776 results on '"Toxoplasmosis pathology"'
Search Results
2. The Toxoplasma secreted effector TgWIP modulates dendritic cell motility by activating host tyrosine phosphatases Shp1 and Shp2.
- Author
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Morales P, Brown AJ, Sangaré LO, Yang S, Kuihon SVNP, Chen B, and Saeij JPJ
- Subjects
- Animals, Humans, Mice, rho-Associated Kinases metabolism, Toxoplasmosis metabolism, Toxoplasmosis parasitology, Toxoplasmosis pathology, Mice, Inbred C57BL, Toxoplasma metabolism, Protein Tyrosine Phosphatase, Non-Receptor Type 11 metabolism, Protein Tyrosine Phosphatase, Non-Receptor Type 11 genetics, Dendritic Cells metabolism, Dendritic Cells parasitology, Cell Movement, Protein Tyrosine Phosphatase, Non-Receptor Type 6 metabolism, Protozoan Proteins metabolism, Protozoan Proteins genetics
- Abstract
The obligate intracellular parasite Toxoplasma gondii causes life-threatening toxoplasmosis to immunocompromised individuals. The pathogenesis of Toxoplasma relies on its swift dissemination to the central nervous system through a 'Trojan Horse' mechanism using infected leukocytes as carriers. Previous work found TgWIP, a protein secreted from Toxoplasma, played a role in altering the actin cytoskeleton and promoting cell migration in infected dendritic cells (DCs). However, the mechanism behind these changes was unknown. Here, we report that TgWIP harbors two SH2-binding motifs that interact with tyrosine phosphatases Shp1 and Shp2, leading to phosphatase activation. DCs infected with Toxoplasma exhibited hypermigration, accompanying enhanced F-actin stress fibers and increased membrane protrusions such as filopodia and pseudopodia. By contrast, these phenotypes were abrogated in DCs infected with Toxoplasma expressing a mutant TgWIP lacking the SH2-binding motifs. We further demonstrated that the Rho-associated kinase (Rock) is involved in the induction of these phenotypes, in a TgWIP-Shp1/2 dependent manner. Collectively, the data uncover a molecular mechanism by which TgWIP modulates the migration dynamics of infected DCs in vitro., (© 2024. The Author(s).)
- Published
- 2024
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3. Observing astrocyte polarization in brains from mouse chronically infected with Toxoplasma gondii.
- Author
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Yao Y, Yuan Y, Sheng S, Li Y, Tang X, and Gu H
- Subjects
- Animals, Mice, Disease Models, Animal, Female, Chronic Disease, Cell Polarity, Glial Fibrillary Acidic Protein metabolism, Glial Fibrillary Acidic Protein genetics, Toxoplasmosis metabolism, Toxoplasmosis parasitology, Toxoplasmosis pathology, Tumor Necrosis Factor-alpha metabolism, Toxoplasmosis, Cerebral parasitology, Toxoplasmosis, Cerebral pathology, Toxoplasmosis, Cerebral metabolism, Astrocytes metabolism, Astrocytes parasitology, Astrocytes pathology, Toxoplasma pathogenicity, Toxoplasma physiology, Brain parasitology, Brain metabolism, Brain pathology
- Abstract
Toxoplasma gondii (T. gondii) is a protozoan parasite that infects approximately one-third of the global human population, often leading to chronic infection. While acute T. gondii infection can cause neural damage in the central nervous system and result in toxoplasmic encephalitis, the consequences of T. gondii chronic infection (TCI) are generally asymptomatic. However, emerging evidence suggests that TCI may be linked to behavioral changes or mental disorders in hosts. Astrocyte polarization, particularly the A1 subtype associated with neuronal apoptosis, has been identified in various neurodegenerative diseases. Nevertheless, the role of astrocyte polarization in TCI still needs to be better understood. This study aimed to establish a mouse model of chronic TCI and examine the transcription and expression levels of glial fibrillary acidic protein (GFAP), C3, C1q, IL-1α, and TNF-α in the brain tissues of the mice. Quantitative real-time PCR (qRT-PCR), enzyme-linked immunosorbent assay, and Western blotting were employed to assess these levels. Additionally, the expression level of the A1 astrocyte-specific marker C3 was evaluated using indirect fluorescent assay (IFA). In mice with TCI, the transcriptional and expression levels of the inflammatory factors C1q, IL-1α, and TNF-α followed an up-down-up pattern, although they remained elevated compared to the control group. These findings suggest a potential association between astrocyte polarization towards the A1 subtype and synchronized changes in these three inflammatory mediators. Furthermore, immunofluorescence assay (IFA) revealed a significant increase in the A1 astrocytes (GFAP
+ C3+ ) proportion in TCI mice. This study provides evidence that TCI can induce astrocyte polarization, a biological process that may be influenced by changes in the levels of three inflammatory factors: C1q, IL-1α, and TNF-α. Additionally, the release of neurotoxic substances by A1 astrocytes may be associated with the development of TCI., (© 2024. The Author(s).)- Published
- 2024
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4. Ileal inflammation is reduced due to treatment with a metalloprotease from BmooMP-α-I snake venom in an experimental model of Toxoplasma gondii infection.
- Author
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Silva TL, Lopes CS, Silva MC, Ferreira FB, Barros HLS, Silva MF, Silva NM, Oliveira F, Mineo TWP, and Mineo JR
- Subjects
- Humans, Animals, Mice, Quality of Life, Mice, Inbred C57BL, Inflammation drug therapy, Metalloproteases, Models, Theoretical, Toxoplasmosis pathology, Toxoplasma, Inflammatory Bowel Diseases
- Abstract
The selection process for advanced therapies in patients with inflammatory bowel diseases (IBDs) must prioritize safety, especially when considering new biologic agents or oral molecule modulators. In C57BL/6 mice, oral infection with Toxoplasma gondii induces intestinal inflammation through excessive tumor necrosis factor (TNF) production, making TNF neutralization a potential therapeutic intervention. Considering this, the present study aimed to evaluate the therapeutic effects of BmooMP-α-I, a snake venom metalloprotease isolated from Bothrops moojeni, which could promote TNF hydrolysis, in treating T. gondii-induced ileitis. The results showed that C57BL/6 mice orally infected with 50 cysts of T. gondii from the Me49 strain and treated with BmooMP-α-I exhibited prolonged survival and improved morbidity scores. Additionally, the treatment ameliorated both the macroscopic and microscopic aspects of the intestine, reduced macrophage influx, and decreased the production of inflammatory mediators by mesenteric lymph node cells. These findings provide compelling experimental evidence supporting the ability of BmooMP-α-I to alleviate ileal inflammation. Considering that the currently available therapeutic protocols are not completely effective and often result in side effects, the exploration of alternative strategies involving novel therapeutic agents, as demonstrated in this study, has the potential to significantly enhance the quality of life for patients suffering from inflammatory bowel diseases., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
- Published
- 2023
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5. Trypanosoma cruzi P21 recombinant protein modulates Toxoplasma gondii infection in different experimental models of the human maternal-fetal interface.
- Author
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de Souza G, Teixeira SC, Fajardo Martínez AF, Silva RJ, Luz LC, de Lima Júnior JP, Rosini AM, Dos Santos NCL, de Oliveira RM, Paschoalino M, Barbosa MC, Alves RN, Gomes AO, da Silva CV, Ferro EAV, and Barbosa BF
- Subjects
- Infant, Newborn, Humans, Female, Pregnancy, Placenta pathology, Interleukin-8, Recombinant Proteins, Trypanosoma cruzi, Toxoplasmosis pathology, Chagas Disease pathology
- Abstract
Introduction: Toxoplasma gondii is the etiologic agent of toxoplasmosis, a disease that affects about one-third of the human population. Most infected individuals are asymptomatic, but severe cases can occur such as in congenital transmission, which can be aggravated in individuals infected with other pathogens, such as HIV-positive pregnant women. However, it is unknown whether infection by other pathogens, such as Trypanosoma cruzi , the etiologic agent of Chagas disease, as well as one of its proteins, P21, could aggravate T. gondii infection., Methods: In this sense, we aimed to investigate the impact of T. cruzi and recombinant P21 (rP21) on T. gondii infection in BeWo cells and human placental explants., Results: Our results showed that T. cruzi infection, as well as rP21, increases invasion and decreases intracellular proliferation of T. gondii in BeWo cells. The increase in invasion promoted by rP21 is dependent on its binding to CXCR4 and the actin cytoskeleton polymerization, while the decrease in proliferation is due to an arrest in the S/M phase in the parasite cell cycle, as well as interleukin (IL)-6 upregulation and IL-8 downmodulation. On the other hand, in human placental villi, rP21 can either increase or decrease T. gondii proliferation, whereas T. cruzi infection increases T. gondii proliferation. This increase can be explained by the induction of an anti-inflammatory environment through an increase in IL-4 and a decrease in IL-6, IL-8, macrophage migration inhibitory factor (MIF), and tumor necrosis factor (TNF)-α production., Discussion: In conclusion, in situations of coinfection, the presence of T. cruzi may favor the congenital transmission of T. gondii , highlighting the importance of neonatal screening for both diseases, as well as the importance of studies with P21 as a future therapeutic target for the treatment of Chagas disease, since it can also favor T. gondii infection., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2023 de Souza, Teixeira, Fajardo Martínez, Silva, Luz, Lima Júnior, Rosini, dos Santos, de Oliveira, Paschoalino, Barbosa, Alves, Gomes, da Silva, Ferro and Barbosa.)
- Published
- 2023
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6. Efficacy of clofazimine against acute and chronic Toxoplasma gondii infection in mice.
- Author
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Biglari-Moghadam N, Najafzadehvarzi H, Gorgani-Firouzjaee T, and Ghasemi-Kasman M
- Subjects
- Animals, Mice, Clofazimine pharmacology, Clofazimine therapeutic use, Persistent Infection, Brain pathology, Zoonoses, Toxoplasma, Toxoplasmosis drug therapy, Toxoplasmosis pathology
- Abstract
Toxoplasmosis is a zoonotic protozoal disease affecting approximately one-third of the world's population. The lack of current treatment options necessitates the development of drugs with good tolerance and effectiveness on the active and cystic stages of the parasite. The present study was established to investigate, for the first time, the potential potency of clofazimine (CFZ) against acute and chronic experimental toxoplasmosis. For this purpose, the type II T. gondii (Me49 strain) was used for induction acute (20 cysts in each mouse) and chronic (10 cysts in each mouse) experimental toxoplasmosis. The mice were treated with 20 mg/kg of CFZ intraperitoneally and orally. The histopathological changes, brain cyst count, total Antioxidant Capacity (TAC), malondialdehyde (MDA) assay, and the level of INF-γ were also evaluated. In the acute toxoplasmosis, both IP and oral administration of CFZ induced a significant reduction in brain parasite burden by 90.2 and 89%, respectively, and increased the survival rate to 100% compared with 60% in untreated controls. In the chronic infection, cyst burden decreased at 85.71 and 76.18% in CFZ-treated subgroups in comparison to infected untreated controls. In addition, 87.5% and 100% of CFZ-treated subgroups survived versus untreated control 62.5%. Moreover, CFZ significantly increased INF-γ levels in acute and chronic toxoplasmosis. Tissue inflammatory lesions were considerably reduced in the CFZ-treated chronic subgroups. CFZ treatment significantly reduced MDA levels and elevated TAC in both acute and chronic infections. In conclusion, CFZ showed a promising finding regarding the ability to reduce cyst burden in acute and chronic infection. Further studies are needed to investigate the therapeutic role of CFZ on toxoplasmosis using the long-term treatment and more advanced approaches. In addition, clofazimine may need to be accompanied by another drug to augment its effect and prevent the regrowth of parasites., Competing Interests: Declaration of competing interest None of the authors have declared conflict of interest., (Copyright © 2023 Elsevier Ltd. All rights reserved.)
- Published
- 2023
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7. Activity of isoflavone biochanin A in chronic experimental toxoplasmosis: impact on inflammation.
- Author
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Aboukamar WA, Elhenawy AA, Elmehankar MS, Elzoheiry MA, El-Gamal R, Elabbasy LM, Hany H, and Nabih N
- Subjects
- Animals, Genistein, Inflammation drug therapy, Mice, RNA, Messenger metabolism, Trimethoprim, Sulfamethoxazole Drug Combination, Tumor Necrosis Factor-alpha genetics, Isoflavones, Toxoplasma genetics, Toxoplasmosis pathology
- Abstract
Toxoplasma gondii is a worldwide prevalent parasite. The infection has been linked to variable inflammatory effects including neuroinflammation. Biochanin A (BCA) is an isoflavone, known for its anti-inflammatory and anti-oxidative properties. In this study, we examined the effect of BCA on the brain and liver inflammatory lesions in a murine model with chronic toxoplasmosis. Mice were divided in to six groups: non-infected control, non-infected BCA-treated, and four infected groups with Toxoplasma gondii Me49-type II cystogenic strain: infected control, BCA (50 mg/kg/day)-treated, combined BCA/cotrimoxazole-treated and cotrimoxazole (370 mg/kg/day) alone-treated. Gene expression of tumor necrosis factor (TNF)-α, interleukin (IL)-1β, and inducible nitric oxide synthase (iNOS) was evaluated by quantitative real-time PCR in the brain and liver tissues. In the infected control group, an upregulation of TNF-α and IL-1β mRNA expression levels was found. However, a downregulation of iNOS expression was detected in the brain of infected control mice. In both BCA- and combined-treated groups, the brain and liver tissues showed significantly reduced inflammatory lesions compared to the infected control mice with inhibited TNF-α and IL-1β mRNA levels. The iNOS expression levels in the brain tissues of BCA group were significantly higher than the levels of the infected control group. BCA alone or combined significantly reduced T. gondii cyst count in the brain tissues. In conclusion, the anti-inflammatory activity of BCA was demonstrated in the brain tissues of mice with chronic toxoplasmosis with decreased TNF-α and IL-1β expression levels and increased iNOS expression levels., (© 2022. The Author(s).)
- Published
- 2022
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8. The correlation of TNF alpha levels with acute phase proteins in acute Toxoplasma gondii infection in mice.
- Author
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Atmaca N and Atmaca HT
- Subjects
- Acute-Phase Proteins, Animals, C-Reactive Protein, Clusterin, Cytokines metabolism, Haptoglobins, Hemopexin, Mice, Tumor Necrosis Factor-alpha, Toxoplasma, Toxoplasmosis pathology, Toxoplasmosis, Animal pathology
- Abstract
Acute Toxoplasma gondii infections can influence the liver as well as other organs. Many cytokines and proteins play a role in the acute response against infection. Tumor necrosis factor alpha (TNF alpha) is a cytokine that plays a key function in stimulating hepatocytes to produce acute phase proteins. In this study, we investigated TNF alpha levels associated with the levels of macroglobulin, haptoglobin, hemopexin, C-reactive protein (CRP), albumin, serum amyloid alpha protein (SAA), and clusterin, which are acute phase proteins, in serum of mice with T. gondii infection. In the experiment, a total of 24 mice were used; 6 mice constituted the control group and 18 mice were infected with the RH strain. On the 2nd, 4th, and 6th days following the infection, 6 animals were euthanized, and their serums were collected. Compared to the control group, we observed a statistically significant decrease in albumin concentration in the group with T. gondii infection on the 6th day. Also, this group displayed a statistically significant, gradual increase in clusterin levels on the 2nd and 6th days, C-reactive protein levels on the 4th day, haptoglobin levels on the 2nd and 4th days, hemopexin levels on the 2nd day, serum amyloid A levels on the 2nd, 4th, and 6th days, and TNF-α levels on the 2nd, 4th, and 6th days (p < 0.05). TNF-α was strongly positively correlated with CRP, SAA, and clusterin, moderately positively correlated with hemopexin, and strongly negatively correlated with albumin. The increase in CRP, SAA, clusterin, and hemopexin levels on the 2nd day after infection, in parallel with the increase in TNF-α levels, indicates that these proteins can be considered as major acute phase proteins in acute T. gondii infection in mice. The data obtained here may be helpful for the diagnosis of T. gondii infection and for monitoring treatments., (Copyright © 2022 Elsevier Inc. All rights reserved.)
- Published
- 2022
- Full Text
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9. Sulfadiazine Plus Pyrimethamine Therapy Reversed Multiple Behavioral and Neurocognitive Changes in Long-Term Chronic Toxoplasmosis by Reducing Brain Cyst Load and Inflammation-Related Alterations.
- Author
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Castaño BL, Silva AA, Hernandez-Velasco LL, Pinheiro APDS, Gibaldi D, Mineo JR, Silva NM, and Lannes-Vieira J
- Subjects
- Animals, Cytokines, Female, Inflammation drug therapy, Memory Disorders parasitology, Mice, Mice, Inbred C57BL, Brain parasitology, Pyrimethamine pharmacology, Pyrimethamine therapeutic use, Sulfadiazine pharmacology, Sulfadiazine therapeutic use, Toxoplasmosis drug therapy, Toxoplasmosis pathology
- Abstract
Toxoplasma gondii infects one-third of the world population. For decades, it has been considered a silent lifelong infection. However, chronically T. gondii -infected persons may present psychiatric and neurocognitive changes as anxiety, depression, and memory loss. In a model of long-term chronic infection, behavioral alterations parallel neuroinflammation and systemic high cytokine levels, and may reflect brain cyst load. Recent findings support that in chronic infection an active parasite-host interplay involves an immune-mediated control of tissue cysts. Here, we tested the idea that etiological treatment in chronic phase may add advantage to intrinsic immune-mediated cyst control and impact behavioral changes. Thus, we combined sulfadiazine-plus-pyrimethamine (S+P), the first-choice therapy for toxoplasmosis, to study the association of brain cyst load and biological processes related to the immune response (neuroinflammation, blood-brain barrier -BBB- disruption and serum cytokine levels), with behavioral and neurocognitive changes of long-term chronic infection. Female C57BL/6 mice (H-2
b ) were infected (5 cysts, ME-49 strain) and treated with S+P from 30 to 60 days postinfection (dpi), compared with vehicle (Veh)-treated and noninfected controls. At endpoints (pre-therapy, 30 dpi; S+P therapy, 60 dpi; after ceased therapy, 90 dpi), independent groups were subjected to behavioral tests, and brain tissues and sera were collected. Multiple behavioral and neurocognitive changes were detected in the early (30 dpi) and long-term (60 and 90 dpi) chronic infection. S+P therapy resolved locomotor alterations, anxiety, and depressive-like behavior, partially or transiently ameliorated hyperactivity and habituation memory loss. Analysis after therapy cessation showed that S+P therapy reduced the number of stimuli required for aversive memory consolidation. S+P therapy resulted in reduced brain cyst load, neuroinflammation and BBB disruption, and lowered systemic Th1-cytokine levels. Correlation analysis revealed association between IFNγ, TNF and MCP-1/CCL2 serum levels, brain cyst load and behavioral and neurocognitive alterations. Moreover, principal-component analysis (PCA-2D and 3D projections) highlighted distinction between clusters (noninfected; Veh-treated and S+P-treated infected). Thus, our data suggest that S+P therapy added gain to intrinsic brain cyst control and, direct or indirectly, ameliorated inflammation-related alterations, traits associated with behavioral and neurocognitive alterations., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2022 Castaño, Silva, Hernandez-Velasco, Pinheiro, Gibaldi, Mineo, Silva and Lannes-Vieira.)- Published
- 2022
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10. Toxoplasma gondii infection induces cell apoptosis via multiple pathways revealed by transcriptome analysis.
- Author
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DU K, Lu F, Xie C, Ding H, Shen Y, Gao Y, Lu S, and Zhuo X
- Subjects
- Animals, Apoptosis, Chlorocebus aethiops, Gene Expression Profiling, Humans, Mammals genetics, Vero Cells, ras GTPase-Activating Proteins genetics, Toxoplasma genetics, Toxoplasmosis genetics, Toxoplasmosis parasitology, Toxoplasmosis pathology
- Abstract
Toxoplasma gondii is a worldwide parasite that can infect almost all kinds of mammals and cause fatal toxoplasmosis in immunocompromised patients. Apoptosis is one of the principal strategies of host cells to clear pathogens and maintain organismal homeostasis, but the mechanism of cell apoptosis induced by T. gondii remains obscure. To explore the apoptosis influenced by T. gondii , Vero cells infected or uninfected with the parasite were subjected to apoptosis detection and subsequent dual RNA sequencing (RNA-seq). Using high-throughput Illumina sequencing and bioinformatics analysis, we found that pro-apoptosis genes such as DNA damage-inducible transcript 3 ( DDIT3 ), growth arrest and DNA damage-inducible α ( GADD45A ), caspase-3 ( CASP3 ), and high-temperature requirement protease A2 ( HtrA2 ) were upregulated, and anti-apoptosis genes such as poly(adenosine diphosphate (ADP)-ribose) polymerase family member 3 ( PARP3 ), B-cell lymphoma 2 ( Bcl-2 ), and baculoviral inhibitor of apoptosis protein (IAP) repeat containing 5 ( BIRC5 ) were downregulated. Besides, tumor necrosis factor (TNF) receptor-associated factor 1 ( TRAF1 ), TRAF2 , TNF receptor superfamily member 10b ( TNFRSF10b ), disabled homolog 2 (DAB2)-interacting protein ( DAB2IP ), and inositol 1,4,5-trisphosphate receptor type 3 ( ITPR3 ) were enriched in the upstream of TNF, TNF-related apoptosis-inducing ligand (TRAIL), and endoplasmic reticulum (ER) stress pathways, and TRAIL-receptor 2 (TRAIL-R2) was regarded as an important membrane receptor influenced by T. gondii that had not been previously considered. In conclusion, the T. gondii RH strain could promote and mediate apoptosis through multiple pathways mentioned above in Vero cells. Our findings improve the understanding of the T. gondii infection process through providing new insights into the related cellular apoptosis mechanisms.
- Published
- 2022
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11. Tbet Expression by Regulatory T Cells Is Needed to Protect against Th1-Mediated Immunopathology during Toxoplasma Infection in Mice.
- Author
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Warunek J, Jin RM, Blair SJ, Garis M, Marzullo B, and Wohlfert EA
- Subjects
- Animals, Female, Forkhead Transcription Factors genetics, Interferon-gamma metabolism, Lymphocyte Activation, Male, Mice, T-Box Domain Proteins genetics, Toxoplasmosis metabolism, Toxoplasmosis pathology, Tumor Necrosis Factor-alpha metabolism, Forkhead Transcription Factors metabolism, T-Box Domain Proteins metabolism, T-Lymphocytes, Regulatory immunology, Toxoplasmosis immunology
- Abstract
Toxoplasma gondii infection has proven to be an ideal model to understand the delicate balance between protective immunity and immune-mediated pathology during infection. Lethal infection causes a collapse of T regulatory cells (Tregs) mediated by the loss of IL-2 and conversion of Tregs to IFN-γ-producing cells. Importantly, these Tregs highly express the Th1 transcription factor Tbet. To determine the role of Tbet in Tregs, we infected Tbx21
f/f -Foxp3YFPCre and control Foxp3YFPCre mice with the type II strain of T. gondii , ME49. The majority of Tbx21f/f -Foxp3YFPCre mice succumbed to a nonlethal dose. Notably, parasite burden was reduced in Tbx21f/f -Foxp3YFPCre compared with Foxp3YFPCre control mice. We found that Tbx21f/f -Foxp3YFPCre mice have significantly higher serum levels of proinflammatory cytokines IFN-γ and TNF-α, suggestive of a heightened immune response. To test if CD4+ T cells were driving immunopathology, we treated Tbx21f/f -Foxp3YFPCre mice with anti-CD4-depleting Abs and partially rescued these mice. Broad-spectrum antibiotic treatment also improved survival, demonstrating a role for commensal flora in immunopathology in Tbx21f/f -Foxp3YFPCre mice. RNA sequencing analysis reinforced that Tbet regulates several key cellular pathways, including leukocyte activation, regulation of lymphocyte activation, and cell cycle progression, that help to maintain fitness in Tregs during Th1 responses. Taken together, our data show an important role for Tbet in Tregs in preventing lethal immunopathology during T. gondii infection, further highlighting the protective role of Treg plasticity in controlling immune responses to infection and the microbiota., (Copyright © 2021 The Authors.)- Published
- 2021
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12. BEWO trophoblast cells and Toxoplasma gondii infection modulate cell death mechanisms in THP-1 monocyte cells by interference in the expression of death receptor and intracellular proteins.
- Author
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da Silva Castro A, Angeloni MB, de Freitas Barbosa B, de Miranda RL, Teixeira SC, Guirelli PM, de Oliveira FC, José da Silva R, Franco PS, Ribeiro M, Milian ICB, de Oliveira Gomes A, Ietta F, Júnior SF, Mineo TWP, Mineo JR, de Oliveira Simões Alves CM, and Ferro EAV
- Subjects
- Caspase 3 metabolism, Cell Death drug effects, Cell Line, Culture Media, Conditioned pharmacology, Down-Regulation drug effects, Fas Ligand Protein metabolism, Humans, MAP Kinase Signaling System drug effects, Macrophage Migration-Inhibitory Factors pharmacology, Monocytes drug effects, Monocytes metabolism, Phosphorylation drug effects, THP-1 Cells, Trophoblasts drug effects, Trophoblasts metabolism, fas Receptor metabolism, Intracellular Space metabolism, Monocytes parasitology, Monocytes pathology, Proteins metabolism, Receptors, Death Domain metabolism, Toxoplasmosis pathology, Trophoblasts parasitology
- Abstract
Crosstalk between trophoblast and monocytes is essential for gestational success, and it can be compromised in congenital toxoplasmosis. Cell death is one of the mechanisms involved in the maintenance of pregnancy, and this study aimed to evaluate the role of trophoblast in the modulation of monocyte cell death in the presence or absence of Toxoplasma gondii infection. THP-1 cells were stimulated with supernatants of BeWo cells and then infected or not with T. gondii. The supernatants were collected and analyzed for the secretion of human Fas ligand, and cells were used to determine cell death and apoptosis, cell death receptor, and intracellular proteins expression. Cell death and apoptosis index were higher in uninfected THP-1 cells stimulated with supernatants of BeWo cells; however, apoptosis index was reduced by T. gondii infection. Macrophage migration inhibitory factor (MIF) and transforming growth factor (TGF)-β1, secreted by BeWo cells, altered the cell death and apoptosis rates in THP-1 cells. In infected THP-1 cells, the expression of Fas/CD95 and secretion of FasL was significantly higher; however, caspase 3 and phosphorylated extracellular-signal-regulated kinase (ERK1/2) were downregulated. Results suggest that soluble factors secreted by BeWo cells induce cell death and apoptosis in THP-1 cells, and Fas/CD95 can be involved in this process. On the other hand, T. gondii interferes in the mechanism of cell death and inhibits THP-1 cell apoptosis, which can be associated with active caspase 3 and phosphorylated ERK1/2. In conclusion, our results showed that human BeWo trophoblast cells and T. gondii infection modulate cell death in human THP-1 monocyte cells., (Copyright © 2021 Elsevier Ltd. All rights reserved.)
- Published
- 2021
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13. Expression of immunoproteasome subunits in the brains of Toxoplasma gondii-infected mice.
- Author
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Zhang Y, Hu W, Liu Q, Ma Z, Hu S, Zhang Z, Jia H, and He X
- Subjects
- Animals, Astrocytes metabolism, Astrocytes pathology, Brain metabolism, Brain microbiology, Brain pathology, Humans, Inflammation microbiology, Inflammation pathology, Interferon-gamma genetics, Interleukin-1beta genetics, Interleukin-6 genetics, Mice, Microglia metabolism, Microglia pathology, Neurons metabolism, Neurons pathology, Toxoplasma genetics, Toxoplasma pathogenicity, Toxoplasmosis microbiology, Toxoplasmosis pathology, Tumor Necrosis Factor-alpha genetics, Inflammation genetics, Proteasome Endopeptidase Complex genetics, Toxoplasmosis genetics
- Abstract
The immunoproteasomes are specific proteasomes that clear oxidant-damaged proteins under inflammatory conditions in various diseases. Toxoplasma gondii (T. gondii) infects the central nervous system and causeencephalitis. However, the relationship between the immunoproteasomes and brain inflammation during T. gondii infection is not well characterized. In this study, we established an in vivo mouse model of T. gondii PLK strain infection via intraperitoneal injection and evaluated the expression of immunoproteasome subunits in the brains of infected mice. The results demonstrated that first, pathological changes in the brains of infected mice increase in severity over time. Second, following T. gondii infection, activated microglia and astrocytes undergo a series of functional alterations and morphological transformations, including proliferation and migration. Third, T. gondii infection induces expression of inflammatory cytokines, including IFN-γ, IL-1β, TNF-α, and IL-6. Fourth, the immunoproteasome subunits low-molecular-weight polypeptide 2 (LMP2), LMP7, and LMP10 mRNA and protein levels are significantly upregulated in T. gondii-infected mouse brains, as shown by RT-qPCR and western blot analysis, compared with that in vehicle-treated brains, and their expression is localized in the microglia, astrocytes, and neurons of T. gondii-infected brains, as determined via immunofluorescence staining. Furthermore, the western blot mean gray value for the immunoproteasome subunits and the positive microglia and astrocyte immunohistochemical signals in the brains of T. gondii-infected mice were positively correlated, indicating that the observed relationships were highly significant. Therefore, it was concluded that the induction of the immunoproteasomes is a pathogenic mechanism underlying T. gondii infection-induced inflammation., (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Published
- 2021
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14. IFN-γ mediates Paneth cell death via suppression of mTOR.
- Author
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Araujo A, Safronova A, Burger E, López-Yglesias A, Giri S, Camanzo ET, Martin AT, Grivennikov S, and Yarovinsky F
- Subjects
- Animals, Female, Interferon-gamma genetics, Intestine, Small parasitology, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Toxoplasma, Toxoplasmosis pathology, Cell Death, Interferon-gamma metabolism, Mechanistic Target of Rapamycin Complex 1 metabolism, Paneth Cells pathology
- Abstract
Paneth cells constitutively produce antimicrobial peptides and growth factors that allow for intestinal homeostasis, host protection, and intestinal stem cell replication. Paneth cells rely heavily on the glycolytic metabolic program, which is in part controlled by the kinase complex Mechanistic target of rapamycin (mTORC1). Yet, little is known about mTOR importance in Paneth cell integrity under steady-state and inflammatory conditions. Our results demonstrate that IFN-γ, a crucial mediator of the intestinal inflammation, acts directly on murine Paneth cells to alter their mitochondrial integrity and membrane potential, resulting in an TORC1-dependent cell death mechanism distinct from canonical cell death pathways including apoptosis, necroptosis, and pyroptosis. These results were established with the purified cytokine and a physiologically relevant common Th1-inducing human parasite Toxoplasma gondii . Given the crucial role for IFN-γ, which is a cytokine frequently associated with the development of inflammatory bowel disease and compromised Paneth cell functions, the identified mechanisms underlying mTORC1-dependent Paneth cell death downstream of IFN-γ may provide promising novel approaches for treating intestinal inflammation., Competing Interests: AA, AS, EB, AL, SG, EC, AM, SG, FY No competing interests declared, (© 2021, Araujo et al.)
- Published
- 2021
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15. ERK1/2 phosphorylation and IL-6 production are involved in the differential susceptibility to Toxoplasma gondii infection in three types of human (cyto/ syncytio/ extravillous) trophoblast cells.
- Author
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Oliveira FC, Silva RJ, Ribeiro M, Guirelli PM, Castro AS, Gomes AO, Franco PS, Teixeira SC, Mineo JR, Barbosa BF, and Ferro EAV
- Subjects
- Cell Differentiation, Cell Line, Tumor, Cell Proliferation, Disease Susceptibility, Extracellular Signal-Regulated MAP Kinases antagonists & inhibitors, Humans, Phosphorylation, Up-Regulation, Extracellular Signal-Regulated MAP Kinases metabolism, Giant Cells pathology, Interleukin-6 biosynthesis, Toxoplasmosis pathology, Trophoblasts parasitology, Trophoblasts pathology
- Abstract
During pregnancy, Toxoplasma gondii can triggers serious manifestations and potentially affect the fetal development. In this scenario, differences in susceptibility of trophoblast cells to T. gondii infection might be evaluated in order to establish new therapeutic approaches capable of interfering in the control of fetal infection by T. gondii. This study aimed to evaluate the susceptibility of cytotrophoblast, syncytiotrophoblast and extravillous trophoblast cells to T. gondii infection. Our data demonstrate that HTR-8/SVneo cells (extravillous trophoblast cells) present higher susceptibility to T. gondii infection when compared to syncytiotrophoblast and cytotrophoblast cells, whereas syncytiotrophoblast was the cell type more resistant to the parasite infection. Also, cytotrophoblast and syncytiotrophoblast cells produced significantly more IL-6 than HTR-8/SVneo cells. On the other hand, HTR-8/SVneo cells showed higher ERK1/2 phosphorylation than cytotrophoblast and syncytiotrophoblast cells. ERK1/2 inhibition reduced T. gondii infection and increased IL-6 production in HTR-8/SVneo cells. Thus, it is plausible to conclude that the greater susceptibility of HTR-8/SVneo cells to infection by T. gondii is related to a higher ERK1/2 phosphorylation and lower levels of IL-6 in these cells compared to other cells, suggesting that these mediators may be important to favor the parasite infection in this type of trophoblastic population., (Copyright © 2021 Elsevier Ltd. All rights reserved.)
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- 2021
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16. Structural insights into an atypical secretory pathway kinase crucial for Toxoplasma gondii invasion.
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Lentini G, Ben Chaabene R, Vadas O, Ramakrishnan C, Mukherjee B, Mehta V, Lunghi M, Grossmann J, Maco B, Visentin R, Hehl AB, Korkhov VM, and Soldati-Favre D
- Subjects
- Biological Transport physiology, Cells, Cultured, Host-Parasite Interactions, Humans, Secretory Pathway physiology, Virulence Factors, Cell Membrane parasitology, Protozoan Proteins metabolism, Receptor Protein-Tyrosine Kinases metabolism, Toxoplasma metabolism, Toxoplasmosis pathology
- Abstract
Active host cell invasion by the obligate intracellular apicomplexan parasites relies on the formation of a moving junction, which connects parasite and host cell plasma membranes during entry. Invading Toxoplasma gondii tachyzoites secrete their rhoptry content and insert a complex of RON proteins on the cytoplasmic side of the host cell membrane providing an anchor to which the parasite tethers. Here we show that a rhoptry-resident kinase RON13 is a key virulence factor that plays a crucial role in host cell entry. Cryo-EM, kinase assays, phosphoproteomics and cellular analyses reveal that RON13 is a secretory pathway kinase of atypical structure that phosphorylates rhoptry proteins including the components of the RON complex. Ultimately, RON13 kinase activity controls host cell invasion by anchoring the moving junction at the parasite-host cell interface.
- Published
- 2021
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17. Dissociating direct and indirect effects: a theoretical framework of how latent toxoplasmosis affects cognitive profile across the lifespan.
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Colzato L, Zhang W, Beste C, and Stock AK
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- Aging metabolism, Chronic Disease, Dopamine metabolism, Humans, Inflammation etiology, Male, Nerve Degeneration etiology, Toxoplasmosis metabolism, Toxoplasmosis pathology, Aging psychology, Cognition, Longevity physiology, Toxoplasmosis psychology
- Abstract
About one-third of the world's population has latent toxoplasmosis, which is typically most prevalent in old age due to its lifelong persistence. Most infected people do not reveal clinically relevant symptoms, but T. gondii might trigger cognitive changes in otherwise asymptomatic individuals. As intact cognitive processes are essential for various achievements and successful aging, this review focuses on the cognitive profile associated with latent toxoplasmosis across the lifespan. It could be explained by a shift in balance between direct effects (increased dopamine synthesis) and indirect effects (neurodegeneration and chronic inflammation, which can decrease dopamine levels). Based thereon, we provide a possibly comprehensive framework of how T. gondii can differently affect cognitive performance across the lifespan (i.e., from increased catecholaminergic signaling in young age to decreased signaling in old age). We outline how future studies may inform our knowledge on the role of individual differences in response to T. gondii and how longitudinal studies can help trace the temporal dynamics in the shift of the balance between direct and indirect effects., (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Published
- 2021
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18. The deubiquitinase OTUB1 augments NF-κB-dependent immune responses in dendritic cells in infection and inflammation by stabilizing UBC13.
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Mulas F, Wang X, Song S, Nishanth G, Yi W, Brunn A, Larsen PK, Isermann B, Kalinke U, Barragan A, Naumann M, Deckert M, and Schlüter D
- Subjects
- Animals, CD11 Antigens metabolism, Dendritic Cells parasitology, Gene Deletion, Interferon-gamma metabolism, Interleukin-12 pharmacology, Lipopolysaccharides, Lysine metabolism, Mice, Inbred C57BL, Mice, Transgenic, Polyubiquitin metabolism, Protein Stability, Sepsis immunology, Sepsis pathology, Toxoplasma physiology, Toxoplasmosis immunology, Toxoplasmosis pathology, Ubiquitination, Up-Regulation, Mice, Cysteine Endopeptidases metabolism, Dendritic Cells immunology, Immunity, Inflammation immunology, NF-kappa B metabolism, Ubiquitin-Conjugating Enzymes metabolism
- Abstract
Dendritic cells (DCs) are indispensable for defense against pathogens but may also contribute to immunopathology. Activation of DCs upon the sensing of pathogens by Toll-like receptors (TLRs) is largely mediated by pattern recognition receptor/nuclear factor-κB (NF-κB) signaling and depends on the appropriate ubiquitination of the respective signaling molecules. However, the ubiquitinating and deubiquitinating enzymes involved and their interactions are only incompletely understood. Here, we reveal that the deubiquitinase OTU domain, ubiquitin aldehyde binding 1 (OTUB1) is upregulated in DCs upon murine Toxoplasma gondii infection and lipopolysaccharide challenge. Stimulation of DCs with the TLR11/12 ligand T. gondii profilin and the TLR4 ligand lipopolysaccharide induced an increase in NF-κB activation in OTUB1-competent cells, resulting in elevated interleukin-6 (IL-6), IL-12, and tumor necrosis factor (TNF) production, which was also observed upon the specific stimulation of TLR2, TLR3, TLR7, and TLR9. Mechanistically, OTUB1 promoted NF-κB activity in DCs by K48-linked deubiquitination and stabilization of the E2-conjugating enzyme UBC13, resulting in increased K63-linked ubiquitination of IRAK1 (IL-1 receptor-associated kinase 1) and TRAF6 (TNF receptor-associated factor 6). Consequently, DC-specific deletion of OTUB1 impaired the production of cytokines, in particular IL-12, by DCs over the first 2 days of T. gondii infection, resulting in the diminished production of protective interferon-γ (IFN-γ) by natural killer cells, impaired control of parasite replication, and, finally, death from chronic T. encephalitis, all of which could be prevented by low-dose IL-12 treatment in the first 3 days of infection. In contrast, impaired OTUB1-deficient DC activation and cytokine production by OTUB1-deficient DCs protected mice from lipopolysaccharide-induced immunopathology. Collectively, these findings identify OTUB1 as a potent novel regulator of DCs during infectious and inflammatory diseases.
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- 2021
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19. Integrin-dependent migratory switches regulate the translocation of Toxoplasma-infected dendritic cells across brain endothelial monolayers.
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Ross EC, Ten Hoeve AL, and Barragan A
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- Animals, Blood-Brain Barrier immunology, Blood-Brain Barrier metabolism, Cell Adhesion, Dendritic Cells metabolism, Endothelium, Vascular immunology, Endothelium, Vascular metabolism, Female, Host-Parasite Interactions, Integrins genetics, Male, Mice, Mice, Inbred C57BL, Toxoplasmosis immunology, Toxoplasmosis metabolism, Toxoplasmosis pathology, Blood-Brain Barrier parasitology, Cell Movement, Dendritic Cells parasitology, Endothelium, Vascular parasitology, Integrins metabolism, Toxoplasma physiology, Toxoplasmosis parasitology
- Abstract
Multiple cellular processes, such as immune responses and cancer cell metastasis, crucially depend on interconvertible migration modes. However, knowledge is scarce on how infectious agents impact the processes of cell adhesion and migration at restrictive biological barriers. In extracellular matrix, dendritic cells (DCs) infected by the obligate intracellular protozoan Toxoplasma gondii undergo mesenchymal-to-amoeboid transition (MAT) for rapid integrin-independent migration. Here, in a cellular model of the blood-brain barrier, we report that parasitised DCs adhere to polarised endothelium and shift to integrin-dependent motility, accompanied by elevated transendothelial migration (TEM). Upon contact with endothelium, parasitised DCs dramatically reduced velocities and adhered under both static and shear stress conditions, thereby obliterating the infection-induced amoeboid motility displayed in collagen matrix. The motility of adherent parasitised DCs on endothelial monolayers was restored by blockade of β1 and β2 integrins or ICAM-1, which conversely reduced motility on collagen-coated surfaces. Moreover, parasitised DCs exhibited enhanced translocation across highly polarised primary murine brain endothelial cell monolayers. Blockade of β1, β2 integrins, ICAM-1 and PECAM-1 reduced TEM frequencies. Finally, gene silencing of the pan-integrin-cytoskeleton linker talin (Tln1) or of β1 integrin (Itgb1) in primary DCs resulted in increased motility on endothelium and decreased TEM. Adding to the paradigms of leukocyte diapedesis, the findings provide novel insights in how an intracellular pathogen impacts the migratory plasticity of leukocytes in response to the cellular environment, to promote infection-related dissemination.
- Published
- 2021
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20. Reduction of Amyloid Burden by Proliferated Homeostatic Microglia in Toxoplasma gondii -Infected Alzheimer's Disease Model Mice.
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Shin JH, Hwang YS, Jung BK, Seo SH, Ham DW, and Shin EH
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- Animals, Mice, Mice, Transgenic, Alzheimer Disease genetics, Alzheimer Disease metabolism, Alzheimer Disease parasitology, Alzheimer Disease pathology, Amyloid beta-Peptides genetics, Amyloid beta-Peptides metabolism, Microglia metabolism, Microglia parasitology, Microglia pathology, Toxoplasma metabolism, Toxoplasmosis genetics, Toxoplasmosis metabolism, Toxoplasmosis pathology
- Abstract
In this study, we confirmed that the number of resident homeostatic microglia increases during chronic Toxoplasma gondii infection. Given that the progression of Alzheimer's disease (AD) worsens with the accumulation of amyloid β (Aβ) plaques, which are eliminated through microglial phagocytosis, we hypothesized that T. gondii -induced microglial proliferation would reduce AD progression. Therefore, we investigated the association between microglial proliferation and Aβ plaque burden using brain tissues isolated from 5XFAD AD mice (AD group) and T. gondii -infected AD mice (AD + Toxo group). In the AD + Toxo group, amyloid plaque burden significantly decreased compared with the AD group; conversely, homeostatic microglial proliferation, and number of plaque-associated microglia significantly increased. As most plaque-associated microglia shifted to the disease-associated microglia (DAM) phenotype in both AD and AD + Toxo groups and underwent apoptosis after the lysosomal degradation of phagocytosed Aβ plaques, this indicates that a sustained supply of homeostatic microglia is required for alleviating Aβ plaque burden. Thus, chronic T. gondii infection can induce microglial proliferation in the brains of mice with progressed AD; a sustained supply of homeostatic microglia is a promising prospect for AD treatment.
- Published
- 2021
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21. Evaluation of Apoptosis, Proliferation, and Adhesion Molecule Expression in Trophoblastic Tissue of Women With Recurrent Spontaneous Abortion and Infected With Toxoplasma gondii.
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Elsalam SA, Mansor AE, Sarhan MH, Shalaby AM, Gobran MA, and Alabiad MA
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- Abortion, Habitual parasitology, Abortion, Spontaneous parasitology, Adult, Antigens, CD genetics, Antigens, CD metabolism, Cadherins genetics, Cadherins metabolism, Cell Adhesion Molecules genetics, Cell Proliferation, Cyclin-Dependent Kinase Inhibitor p27 genetics, Cyclin-Dependent Kinase Inhibitor p27 metabolism, Female, Humans, Hyaluronan Receptors genetics, Hyaluronan Receptors metabolism, Immunohistochemistry, Ki-67 Antigen genetics, Ki-67 Antigen metabolism, Placenta parasitology, Placenta pathology, Pregnancy, Proto-Oncogene Proteins c-bcl-2 genetics, Proto-Oncogene Proteins c-bcl-2 metabolism, Toxoplasma isolation & purification, Toxoplasmosis parasitology, Trophoblasts parasitology, Trophoblasts pathology, bcl-2-Associated X Protein genetics, bcl-2-Associated X Protein metabolism, Abortion, Habitual pathology, Abortion, Spontaneous pathology, Apoptosis, Cell Adhesion Molecules metabolism, Toxoplasma immunology, Toxoplasmosis pathology
- Abstract
Recurrent spontaneous abortion is an obstetric complication with undefined causes. Apoptosis, proliferation, and adhesion are considered important factors in the pathogenesis of abortion. This work aimed to determine Bax and Bcl-2 as a proapoptotic and antiapoptotic protein, Ki67 and P27kip as proliferative and antiproliferative proteins, and E-cadherin and CD44 as adhesion molecules in the trophoblastic tissues in cases with recurrent miscarriage. Immunohistochemistry and quantitative polymerase chain reaction analysis of Bax, Bcl-2, Ki67, P27kip, E-cadherin, and CD44 in paraffin-embedded sections of placental tissues obtained from 108 women were divided into 3 categories: 66 Toxoplasma gondii-positive women with recurrent abortion, 22 T. gondii-negative women with recurrent abortion, and 20 women with no history of abortion as a control group. The mean ratio of the expression of Bax and P27kip proteins was 35.3% and 36.1%, which is significantly higher than that of the second group (19.88 and 20.02%), and the third group (12.3% and 10.98%), while the mean ratio of the expression of Bcl-2, Ki67, E-cadherin, and CD44 proteins was 12.35%, 11.23%, 10.32%, and 9.97%, which is significantly lower than that of the second group (33.75%, 13.18%, 21.88%, and 23.29%) and that of the third group (38.58%, 39.27%, 37.98%, and 35.79%). The presence of proapoptotic protein (Bax) and antiproliferative protein (P27kip) at high levels and the presence of antiapoptotic protein (Bcl-2), proliferative protein (Ki67), and adhesion molecules (E-cadherin and CD44) in lower levels in the T. gondii-positive group clarify the mechanism involved in the induction of abortion and loss of pregnancy., Competing Interests: The authors declare no conflict of interest., (Copyright © 2020 by the International Society of Gynecological Pathologists.)
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- 2021
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22. Toxoplasmosis: Recent Advances in Understanding the Link Between Infection and Host Behavior.
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Johnson SK and Johnson PTJ
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- Animals, Brain parasitology, Humans, Toxoplasmosis complications, Toxoplasmosis transmission, Behavior, Host-Parasite Interactions, Toxoplasma pathogenicity, Toxoplasmosis pathology
- Abstract
Humans, wildlife, and domestic animals are intimately linked through shared infections. Many parasites and pathogens use multiple host species, either opportunistically or sequentially, such that managing disease risk frequently requires a broader understanding of the ecological community. The coccidian protozoan Toxoplasma gondii infects more than one hundred species of vertebrates, ranging from bats to beluga whales. In humans, acute toxoplasmosis can have serious health consequences for immunocompromised individuals. Even amongst asymptomatic patients, however, toxoplasmosis has been linked to a range of behavioral alterations and conditions, such as changes in risk tolerance, neuroticism, mental illness, suicide, and accident proneness. Whether such links are causal or simply correlational has been the subject of intense study and debate; from an evolutionary standpoint, selection may favor parasite-induced alterations in host behavior that increase the likelihood a host is consumed by the definitive host-in this case a domestic or wild felid. Here, we examine current evidence for parasite-induced manipulations of host behavior, in both humans and other animals. We critically evaluate proposed mechanisms through which infection might influence host behavior, which range from inflammation in the brain to changes in hormones or neurotransmitters. Considering estimates that T. gondii may infect up to one-third of the global human population, we conclude by examining the implications of these changes for human behavior, individual fitness, and emergent cultural properties.
- Published
- 2021
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23. A brain cyst load-associated antigen is a Toxoplasma gondii biomarker for serodetection of persistent parasites and chronic infection.
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Dard C, Swale C, Brenier-Pinchart MP, Farhat DC, Bellini V, Robert MG, Cannella D, Pelloux H, Tardieux I, and Hakimi MA
- Subjects
- Animals, Biomarkers metabolism, Chronic Disease, Mice, Serologic Tests, Toxoplasmosis parasitology, Toxoplasmosis pathology, Brain parasitology, Toxoplasma physiology, Toxoplasmosis diagnosis
- Abstract
Background: Biomarker discovery remains a major challenge for predictive medicine, in particular, in the context of chronic diseases. This is true for the widespread protozoan Toxoplasma gondii which establishes long-lasting parasitism in metazoans, humans included. This microbe successively unfolds distinct genetic programs that direct the transition from high to low replicative potential inside host cells. As a slow-replicating cell, the T. gondii bradyzoite developmental stage persists enclosed in a cyst compartment within tissues including the nervous system, being held by a sustained immune equilibrium which accounts for the prolonged clinically silent phase of parasitism. Serological surveys indicate that nearly one third of the human population has been exposed to T. gondii and possibly host bradyzoites. Because any disruption of the immune balance drives the reverse transition from bradyzoite to fast replicating tachyzoite and uncontrolled growth of the latter, these people are at risk for life-threatening disease. While serological tests for discriminating recent from past infection are available, there is yet no immunogenic biomarker used in the serological test to allow ascertaining the presence of persistent bradyzoites., Results: Capitalizing on genetically engineered parasites induced to produce mature bradyzoites in vitro, we have identified the BCLA/MAG2 protein being restricted to the bradyzoite and the cyst envelope. Using laboratory mice as relevant T. gondii host models, we demonstrated that BCLA/MAG2 drives the generation of antibodies that recognize bradyzoite and the enveloping cyst structure. We have designed an ELISA assay based on a bacterially produced BCLA recombinant polypeptide, which was validated using a large collection of sera from mice of different genetic backgrounds and infected with bcla+ or bcla-null cystogenic and non-cystogenic T. gondii strains. To refine the design of the ELISA assay, we applied high-resolution BCLA epitope mapping and identified a specific combination of peptides and accordingly set up a selective and sensitive ELISA assay which allowed the detection of anti-BCLA/MAG2 antibodies in the sera of human patients with various forms of toxoplasmosis., Conclusions: We brought proof of principle that anti-BCLA/MAG2 antibodies serve as specific and sensitive serological markers in the perspective of a combinatorial strategy for detection of persistent T. gondii parasitism.
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- 2021
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24. Clinical manifestations and visual outcomes associated with ocular toxoplasmosis in a Brazilian population.
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Arruda S, Vieira BR, Garcia DM, Araújo M, Simões M, Moreto R, Rodrigues MW Jr, Belfort R Jr, Smith JR, and Furtado JM
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- Adolescent, Adult, Age Factors, Aged, Antibodies, Protozoan blood, Antiprotozoal Agents therapeutic use, Blindness drug therapy, Blindness immunology, Blindness parasitology, Brazil, Female, Humans, Immunoglobulin G blood, Immunoglobulin M blood, Male, Middle Aged, Pyrimethamine therapeutic use, Recurrence, Retina drug effects, Retina immunology, Retina parasitology, Retina pathology, Risk Factors, Sulfadiazine therapeutic use, Toxoplasma drug effects, Toxoplasma growth & development, Toxoplasmosis drug therapy, Toxoplasmosis immunology, Toxoplasmosis parasitology, Treatment Outcome, Trimethoprim, Sulfamethoxazole Drug Combination therapeutic use, Uveitis, Posterior drug therapy, Uveitis, Posterior immunology, Uveitis, Posterior parasitology, Vision, Ocular drug effects, Visual Acuity drug effects, Blindness pathology, Toxoplasma pathogenicity, Toxoplasmosis pathology, Uveitis, Posterior pathology
- Abstract
Ocular toxoplasmosis is the leading cause of posterior uveitis worldwide. We conducted an observational study of 262 consecutive individuals (n = 344 eyes) with ocular toxoplasmosis who were followed over a 34-month period. Most subjects were T. gondii IgG + /IgM- (n = 242; 92.4%; 317 eyes), and 140 eyes (40.7%) had active lesions. For eyes in which retinal lesions were active at recruitment and best-corrected visual acuity (BCVA) could be measured (n = 133), 21.0% (n = 28) remained blind (BCVA below 20/400) after inflammation resolved. In these eyes, atypical ocular toxoplasmosis (OR 4.99; 95% CI 1.14-22.85; p = 0.0330), macular lesion (OR 9.95; 95% CI 2.45-47.15; p = 0.0019) and any complication (OR 10.26; 95% CI 3.82-30.67; p < 0.0001) were associated with BCVA below 20/200. For eyes with only inactive lesions at recruitment and BCVA measured (n = 178), 28.1% (n = 50) were blind. In these eyes, having at least one lesion larger than one disc-diameter (OR 6.30; 95% CI 2.28-22.46; p = 0.0013) and macular lesion (OR 5.69; 95% CI 2.53-13.54; p < 0.0001) were associated with BCVA below 20/200. Older age (OR 1.02; 95% CI 1.00-1.05; p = 0.0493) and active disease at presentation (OR 4.74; 95% CI 1.95-12.91; p = 0.0011) were associated with recurrences. Additional clinical attention should be directed towards patients with risk factors for poor visual outcome.
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- 2021
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25. Stem cell-derived enteroid cultures as a tool for dissecting host-parasite interactions in the small intestinal epithelium.
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Hares MF, Tiffney EA, Johnston LJ, Luu L, Stewart CJ, Flynn RJ, and Coombes JL
- Subjects
- Animals, Cell Culture Techniques, Coccidiosis parasitology, Cryptosporidium pathogenicity, Humans, Models, Biological, Neospora physiology, Stem Cells parasitology, Toxoplasma pathogenicity, Cryptosporidiosis pathology, Cryptosporidium physiology, Host-Parasite Interactions, Intestinal Mucosa parasitology, Toxoplasma physiology, Toxoplasmosis pathology
- Abstract
Toxoplasma gondii and Cryptosporidium spp. can cause devastating pathological effects in humans and livestock, and in particular to young or immunocompromised individuals. The current treatment plans for these enteric parasites are limited due to long drug courses, severe side effects or simply a lack of efficacy. The study of the early interactions between the parasites and the site of infection in the small intestinal epithelium has been thwarted by the lack of accessible, physiologically relevant and species-specific models. Increasingly, 3D stem cell-derived enteroid models are being refined and developed into sophisticated models of infectious disease. In this review, we shall illustrate the use of enteroids to spearhead research into enteric parasitic infections, bridging the gap between cell line cultures and in vivo experiments., (© 2020 John Wiley & Sons Ltd.)
- Published
- 2021
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26. Toxoplasma gondii infection impairs the colonic motility of rats due to loss of myenteric neurons.
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Machado CCA, Watanabe PDS, Mendes JDL, Pupim ACE, Ortigoza SM, Bergoc HG, Nino BSL, Góis MB, Garcia JL, Blackshaw LA, Sant Ana DMG, and Araújo EJA
- Subjects
- Animals, Colon physiopathology, Muscle, Smooth physiopathology, Myenteric Plexus, Myoelectric Complex, Migrating physiology, Rats, Toxoplasmosis pathology, Colon innervation, Gastrointestinal Motility physiology, Muscle, Smooth innervation, Neurons pathology, Toxoplasmosis physiopathology
- Abstract
Background: Toxoplasma gondii infection causes intestinal inflammation and diarrhea indicating possible intestinal motor dysfunction. Anatomical studies have shown alterations in the colonic myenteric plexus, but it is unknown whether this impacts motility and therefore whether motility is a target for treatment. We determined whether colonic coordinated movements are compromised by toxoplasmic infection and how it is associated with anatomical changes., Methods: Male Wistar rats were evaluated at 6, 12, 24, 48, and 72 hours and 30 days postinfection (dpi) and controls. Infected rats received orally 5 × 10
3 sporulated oocysts of strain ME-49 (genotype II) of T gondii. The colon was collected for anatomical analysis (including the myenteric plexus immunolabeled with HuC/D, nNOS, and ChAT) and motility analysis in vitro (conventional manometry). Fecal output was measured daily., Key Results: At 12 hours postinfection, T gondii caused hypertrophy of the muscularis externa layer of the distal colon. There was loss of total, nitrergic, and cholinergic myenteric neurons in the proximal colon at 30 day postinfection (dpi); however, only loss of cholinergic neurons was found in the distal colon. Contractile complexes in the middle and distal colon were longer in duration in infected animals, which was associated with slower migration of the colonic motor complex. However, gastrointestinal transit time and fecal pellet output remained unchanged during the T gondii infection., Conclusions and Inferences: Toxoplasma gondii caused myenteric neuronal loss in the proximal and distal colon and altered the motility pattern in the middle and distal colon to a more propulsive phenotype., (© 2020 John Wiley & Sons Ltd.)- Published
- 2021
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27. Codetection of pulmonary tuberculosis and toxoplasmosis in a pediatric bronchoalveolar lavage specimen: A cytologist's assistance to clinical management.
- Author
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Vasantham V, Singh G, Jahan A, Gupta R, Dogra RK, Sarin N, and Singh S
- Subjects
- Azure Stains administration & dosage, Bronchoalveolar Lavage methods, Child, Humans, Lymphocytes parasitology, Male, Toxoplasma pathogenicity, Toxoplasmosis diagnosis, Toxoplasmosis pathology, Tuberculosis, Pulmonary diagnosis, Tuberculosis, Pulmonary pathology
- Abstract
Background: Toxoplasmosis causes serious and sometimes life-threatening disease in immunocompromised patients like organ transplant recipients, immunodeficiency disorders or HIV-infected individuals. The co-occurrence of toxoplasmosis in a respiratory sample harboring tuberculosis (TB) may be missed especially in an area endemic for the latter infection., Case Report: A 10-year-old child presented with complaints of fever with loss of appetite and weight. Based on radiological and clinical features, a presumptive diagnosis of pulmonary TB was made and bronchoalveolar lavage (BAL) performed for cytological and microbiological confirmation. Smears from BAL showed numerous lymphocytes along with few ciliated columnar epithelial cells. Ziehl-Neelsen stain for acid-fast bacilli was positive. The Giemsa-stained cytosmears also showed clusters of crescent-shaped tachyzoites of toxoplasma gondii in a background of lymphocytes. The patient was initiated on anti-tubercular therapy with marked clinical improvement., Conclusion: A diligent screening of cytosmears for a possible coinfection in a TB-positive sample is essential for the cytopathologists to detect coexisting toxoplasmosis, which is a rare but treatable disease., (© 2020 Wiley Periodicals LLC.)
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- 2021
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28. Trypanosoma cruzi and Toxoplasma gondii Induce a Differential MicroRNA Profile in Human Placental Explants.
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Medina L, Castillo C, Liempi A, Guerrero-Muñoz J, Rojas-Pirela M, Maya JD, Prieto H, and Kemmerling U
- Subjects
- Female, Humans, Pregnancy, Chagas Disease immunology, Chagas Disease pathology, Gene Expression Regulation immunology, MicroRNAs immunology, Placenta immunology, Placenta parasitology, Placenta pathology, Toxoplasma immunology, Toxoplasmosis immunology, Toxoplasmosis pathology, Trypanosoma cruzi immunology
- Abstract
Trypanosoma cruzi and Toxoplasma gondii are two parasites than can be transmitted from mother to child through the placenta. However, congenital transmission rates are low for T. cruzi and high for T. gondii . Infection success or failure depends on complex parasite-host interactions in which parasites can alter host gene expression by modulating non-coding RNAs such as miRNAs. As of yet, there are no reports on altered miRNA expression in placental tissue in response to either parasite. Therefore, we infected human placental explants ex vivo by cultivation with either T. cruzi or T. gondii for 2 h. We then analyzed the miRNA expression profiles of both types of infected tissue by miRNA sequencing and quantitative PCR, sequence-based miRNA target prediction, pathway functional enrichment, and upstream regulator analysis of differentially expressed genes targeted by differentially expressed miRNAs. Both parasites induced specific miRNA profiles. GO analysis revealed that the in silico predicted targets of the differentially expressed miRNAs regulated different cellular processes involved in development and immunity, and most of the identified KEGG pathways were related to chronic diseases and infection. Considering that the differentially expressed miRNAs identified here modulated crucial host cellular targets that participate in determining the success of infection, these miRNAs might explain the differing congenital transmission rates between the two parasites. Molecules of the different pathways that are regulated by miRNAs and modulated during infection, as well as the miRNAs themselves, may be potential targets for the therapeutic control of either congenital Chagas disease or toxoplasmosis., (Copyright © 2020 Medina, Castillo, Liempi, Guerrero-Muñoz, Rojas-Pirela, Maya, Prieto and Kemmerling.)
- Published
- 2020
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29. Effects of Toxoplasma gondii infection on the function and integrity of human cerebrovascular endothelial cells and the influence of verapamil treatment in vitro.
- Author
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Harun MSR, Marsh V, Elsaied NA, Webb KF, and Elsheikha HM
- Subjects
- Blood-Brain Barrier drug effects, Blood-Brain Barrier metabolism, Brain drug effects, Brain metabolism, Brain physiopathology, Cells, Cultured, Endothelial Cells metabolism, Endothelial Cells pathology, Humans, Toxoplasmosis metabolism, Toxoplasmosis pathology, Blood-Brain Barrier physiopathology, Calcium Channel Blockers pharmacology, Endothelial Cells drug effects, Toxoplasmosis physiopathology, Verapamil pharmacology
- Abstract
Toxoplasma gondii can cause parasitic encephalitis, a life-threatening infection that predominately occurs in immunocompromised individuals. T. gondii has the ability to invade the brain, but the mechanisms by which this parasite crosses the blood-brain-barrier (BBB) remain incompletely understood. The present study reports the changes associated with infection and replication of T. gondii within human brain microvascular endothelial cells (BMECs) in vitro. Our results indicated that exposure to T. gondii had an adverse impact on the function and integrity of the BMECs - through induction of cell cycle arrest, disruption of the BMEC barrier integrity, reduction of cellular viability and vitality, depolarization of the mitochondrial membrane potential, increase of the DNA fragmentation, and alteration of the expression of immune response and tight junction genes. The calcium channel/P-glycoprotein transporter inhibitor verapamil was effective in inhibiting T. gondii crossing the BMECs in a dose-dependent manner. The present study showed that T. gondii can compromise several functions of BMECs and demonstrated the ability of verapamil to inhibit T. gondii crossing of the BMECs in vitro., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)
- Published
- 2020
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30. Granulomas in parasitic diseases: the good and the bad.
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Giorgio S, Gallo-Francisco PH, Roque GAS, and Flóro E Silva M
- Subjects
- Animals, Granuloma parasitology, Host-Parasite Interactions immunology, Humans, Macrophages pathology, Neurocysticercosis pathology, Schistosoma mansoni immunology, Schistosomiasis mansoni pathology, Taenia solium immunology, Toxoplasma immunology, Toxoplasmosis pathology, Granuloma immunology, Granuloma pathology, Macrophages immunology, Neurocysticercosis immunology, Schistosomiasis mansoni immunology, Toxoplasmosis immunology
- Abstract
Parasitic diseases affect more than one billion people worldwide, and most of them are chronic conditions in which the treatment and prevention are difficult. The appearance of granulomas, defined as organized and compact structures of macrophages and other immune cells, during various parasitic diseases is frequent, since these structures will only form when individual immune cells do not control the invading agent. Th2-typering various parasitic diseases are frequent, since these structures will only form when individual immune cells do not control the invading agent. The characterization of granulomas in different parasitic diseases, as well as recent findings in this field, is discussed in this review, in order to understand the significance of the granuloma and its modulation in the host-parasite interaction and in the immune, pathological, and parasitological aspects of this interaction. The parasitic granulomatous diseases granulomatous amebic encephalitis, toxoplasmosis, leishmaniasis, neurocysticercosis, and schistosomiasis mansoni are discussed as well as the mechanistic and dynamical aspects of the infectious granulomas.
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- 2020
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31. Toxoplasma infection induces microglia-neuron contact and the loss of perisomatic inhibitory synapses.
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Carrillo GL, Ballard VA, Glausen T, Boone Z, Teamer J, Hinkson CL, Wohlfert EA, Blader IJ, and Fox MA
- Subjects
- Animals, Female, Male, Mice, Mice, Inbred C57BL, Mice, Transgenic, Microglia parasitology, Microglia pathology, Neurons parasitology, Neurons pathology, Synapses parasitology, Synapses pathology, Toxoplasma, Toxoplasmosis pathology, Cell Communication physiology, Microglia metabolism, Neural Inhibition physiology, Neurons metabolism, Synapses metabolism, Toxoplasmosis metabolism
- Abstract
Infection and inflammation within the brain induces changes in neuronal connectivity and function. The intracellular protozoan parasite, Toxoplasma gondii, is one pathogen that infects the brain and can cause encephalitis and seizures. Persistent infection by this parasite is also associated with behavioral alterations and an increased risk for developing psychiatric illness, including schizophrenia. Current evidence from studies in humans and mouse models suggest that both seizures and schizophrenia result from a loss or dysfunction of inhibitory synapses. In line with this, we recently reported that persistent T. gondii infection alters the distribution of glutamic acid decarboxylase 67 (GAD67), an enzyme that catalyzes GABA synthesis in inhibitory synapses. These changes could reflect a redistribution of presynaptic machinery in inhibitory neurons or a loss of inhibitory nerve terminals. To directly assess the latter possibility, we employed serial block face scanning electron microscopy (SBFSEM) and quantified inhibitory perisomatic synapses in neocortex and hippocampus following parasitic infection. Not only did persistent infection lead to a significant loss of perisomatic synapses, it induced the ensheathment of neuronal somata by myeloid-derived cells. Immunohistochemical, genetic, and ultrastructural analyses revealed that these myeloid-derived cells included activated microglia. Finally, ultrastructural analysis identified myeloid-derived cells enveloping perisomatic nerve terminals, suggesting they may actively displace or phagocytose synaptic elements. Thus, these results suggest that activated microglia contribute to perisomatic inhibitory synapse loss following parasitic infection and offer a novel mechanism as to how persistent T. gondii infection may contribute to both seizures and psychiatric illness., (© 2020 Wiley Periodicals, Inc.)
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- 2020
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32. T. gondii infection induces IL-1R dependent chronic cachexia and perivascular fibrosis in the liver and skeletal muscle.
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Melchor SJ, Hatter JA, Castillo ÉAL, Saunders CM, Byrnes KA, Sanders I, Abebayehu D, Barker TH, and Ewald SE
- Subjects
- Animals, Cachexia metabolism, Cachexia pathology, Disease Models, Animal, Fibrosis metabolism, Fibrosis pathology, Hepatic Stellate Cells drug effects, Hepatic Stellate Cells metabolism, Interleukin-1alpha pharmacology, Liver Cirrhosis metabolism, Liver Cirrhosis pathology, Mice, Muscle, Skeletal metabolism, Muscle, Skeletal pathology, Muscular Atrophy metabolism, Muscular Atrophy parasitology, Muscular Atrophy pathology, Myofibroblasts drug effects, Myofibroblasts metabolism, Signal Transduction physiology, Toxoplasmosis metabolism, Toxoplasmosis pathology, Cachexia parasitology, Liver Cirrhosis parasitology, Muscle, Skeletal parasitology, Receptors, Interleukin-1 metabolism, Toxoplasmosis complications
- Abstract
Cachexia is a progressive muscle wasting disease that contributes to death in a wide range of chronic diseases. Currently, the cachexia field lacks animal models that recapitulate the long-term kinetics of clinical disease, which would provide insight into the pathophysiology of chronic cachexia and a tool to test therapeutics for disease reversal. Toxoplasma gondii (T. gondii) is a protozoan parasite that uses conserved mechanisms to infect rodents and human hosts. Infection is lifelong and has been associated with chronic weight loss and muscle atrophy in mice. We have recently shown that T. gondii-induced muscle atrophy meets the clinical definition of cachexia. Here, the longevity of the T. gondii-induced chronic cachexia model revealed that cachectic mice develop perivascular fibrosis in major metabolic organs, including the adipose tissue, skeletal muscle, and liver by 9 weeks post-infection. Development of cachexia, as well as liver and skeletal muscle fibrosis, is dependent on intact signaling through the type I IL-1R receptor. IL-1α is sufficient to activate cultured fibroblasts and primary hepatic stellate cells (myofibroblast precursors in the liver) in vitro, and IL-1α is elevated in the sera and liver of cachectic, suggesting a mechanism by which chronic IL-1R signaling could be leading to cachexia-associated fibrosis.
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- 2020
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33. Toxoplasma gondii infection damages the perineuronal nets in a murine model.
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Meurer YDSR, Brito RMM, da Silva VP, Andade JMA, Linhares SSG, Pereira Junior A, de Andrade-Neto VF, de Sá AL, and Oliveira CBS
- Subjects
- Animals, Cerebellum cytology, Disease Models, Animal, Mice, Motor Neurons metabolism, Neurons metabolism, Toxoplasma, Toxoplasmosis metabolism, Cerebellum metabolism, Extracellular Matrix metabolism, Motor Neurons cytology, Neurons pathology, Toxoplasmosis pathology, Toxoplasmosis, Animal
- Abstract
Background: Behavioral and neurochemical alterations associated with toxoplasmosis may be influenced by the persistence of tissue cysts and activation of an immune response in the brain of Toxoplasma gondii-infected hosts. The cerebral extracellular matrix is organised as perineuronal nets (PNNs) that are both released and ensheath by some neurons and glial cells. There is evidences to suggest that PNNs impairment is a pathophysiological mechanism associated with neuropsychiatric conditions. However, there is a lack of information regarding the impact of parasitic infections on the PNNs integrity and how this could affect the host's behavior., Objectives: In this context, we aimed to analyse the impact of T. gondii infection on cyst burden, PNNs integrity, and possible effects in the locomotor activity of chronically infected mice., Methods: We infected mice with T. gondii ME-49 strain. After thirty days, we assessed locomotor performance of animals using the open field test, followed by evaluation of cysts burden and PNNs integrity in four brain regions (primary and secondary motor cortices, prefrontal and somesthetic cortex) to assess the PNNs integrity using Wisteria floribunda agglutinin (WFA) labeling by immunohistochemical analyses., Findings and Main Conclusions: Our findings revealed a random distribution of cysts in the brain, the disruption of PNNs surrounding neurons in four areas of the cerebral cortex and hyperlocomotor behavior in T. gondii-infected mice. These results can contribute to elucidate the link toxoplasmosis with the establishment of neuroinflammatory response in neuropsychiatric disorders and to raise a discussion about the mechanisms related to changes in brain connectivity, with possible behavioral repercussions during chronic T. gondii infection.
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- 2020
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34. Neuroprotective Effect of Chronic Intracranial Toxoplasma gondii Infection in a Mouse Cerebral Ischemia Model.
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Lee SH, Jung BK, Song H, Seo HG, Chai JY, and Oh BM
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- Animals, Brain cytology, Brain metabolism, Brain pathology, Brain Ischemia parasitology, Brain Ischemia pathology, Disease Models, Animal, Gene Expression, Hypoxia-Inducible Factor 1, alpha Subunit genetics, Mice, Inbred ICR, Organ Size, Toxoplasmosis metabolism, Toxoplasmosis pathology, Brain parasitology, Brain Ischemia prevention & control, Host-Parasite Interactions, Hypoxia-Inducible Factor 1, alpha Subunit metabolism, Neuroprotection, Toxoplasma physiology, Toxoplasmosis physiopathology
- Abstract
Toxoplasma gondii is an obligate intracellular protozoan parasite that can invade various organs in the host body, including the central nervous system. Chronic intracranial T. gondii is known to be associated with neuroprotection against neurodegenerative diseases through interaction with host brain cells in various ways. The present study investigated the neuroprotective effects of chronic T. gondii infection in mice with cerebral ischemia experimentally produced by middle cerebral artery occlusion (MCAO) surgery. The neurobehavioral effects of cerebral ischemia were assessed by measurement of Garcia score and Rotarod behavior tests. The volume of brain ischemia was measured by triphenyltetrazolium chloride staining. The expression levels of related genes and proteins were determined. After cerebral ischemia, corrected infarction volume was significantly reduced in T. gondii infected mice, and their neurobehavioral function was significantly better than that of the uninfection control group. Chronic T. gondii infection induced the expression of hypoxia-inducible factor 1-alpha (HIF-1α) in the brain before MCAO. T. gondii infection also increased the expression of vascular endothelial growth factor after the cerebral ischemia. It is suggested that chronic intracerebral infection of T. gondii may be a potential preconditioning strategy to reduce neural deficits associated with cerebral ischemia and induce brain ischemic tolerance through the regulation of HIF-1α expression.
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- 2020
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35. A negative covariation between toxoplasmosis and CoVID-19 with alternative interpretations.
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Jankowiak Ł, Rozsa L, Tryjanowski P, and Møller AP
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- Betacoronavirus isolation & purification, COVID-19, Coronavirus Infections epidemiology, Coronavirus Infections virology, Disease Susceptibility economics, Humans, Linear Models, Pandemics, Pneumonia, Viral epidemiology, Pneumonia, Viral virology, Prevalence, SARS-CoV-2, Toxoplasmosis epidemiology, Toxoplasmosis parasitology, Coronavirus Infections pathology, Pneumonia, Viral pathology, Toxoplasmosis pathology
- Abstract
Coronaviruses may exert severely negative effects on the mortality and morbidity of birds and mammals including humans and domestic animals. Most recently CoVID-19 has killed about half million people (27th of June, 2020). Susceptibility to this disease appears to differ markedly across different societies but the factors underlying this variability are not known. Given that prevalence of toxoplasmosis in human societies may serve as a proxy for hygiene, and it also exerts both direct and immune-mediated antiviral effects, we hypothesize a negative covariation between toxoplasmosis and measures of the CoVID-19 pandemic across countries. We obtained aged-adjusted toxoplasmosis prevalence of pregnant women from the literature. Since the differences in the CoVID-19 morbidity and mortality may depend on the different timing of the epidemics in each country, we applied the date of first documented CoVID-19 in each country as a proxy of susceptibility, with a statistical control for population size effects. Using these two indices, we show a highly significant negative co-variation between the two pandemics across 86 countries. Then, considering that the wealth of nations often co-varies with the prevalence of diseases, we introduced GDP per capita into our model. The prevalence of toxoplasmosis co-varies negatively, while the date of first CoVID-19 co-varies positively with GDP per capita across countries. Further, to control for the strong spatial autocorrelation among countries, we carried out a Spatial Structure Analyses of the relationships between the date of first CoVID-19, prevalence of toxoplasmosis, and GDP per capita. Results of this analysis did not confirm a direct causal relationship between toxoplasmosis and susceptibility to the CoVID-19 pandemics. As far as an analysis of observational data let us to suggest, it appears that the interaction between CoVID-19 and toxoplasmosis is mediated by GDP per capita and spatial effects. This prompts the question whether the formerly known covariations of CoVID-19 and BCG vaccination or air pollution might have also emerged as spurious indirect effects.
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- 2020
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36. Catastrophic consequences: can the feline parasite Toxoplasma gondii prompt the purrfect neuroinflammatory storm following traumatic brain injury?
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Baker TL, Sun M, Semple BD, Tyebji S, Tonkin CJ, Mychasiuk R, and Shultz SR
- Subjects
- Animals, Brain microbiology, Brain pathology, Cats, Humans, Inflammation, Toxoplasma, Brain Injuries, Traumatic microbiology, Brain Injuries, Traumatic pathology, Brain Injuries, Traumatic physiopathology, Toxoplasmosis complications, Toxoplasmosis pathology
- Abstract
Traumatic brain injury (TBI) is one of the leading causes of morbidity and mortality worldwide; however, treatment development is hindered by the heterogenous nature of TBI presentation and pathophysiology. In particular, the degree of neuroinflammation after TBI varies between individuals and may be modified by other factors such as infection. Toxoplasma gondii, a parasite that infects approximately one-third of the world's population, has a tropism for brain tissue and can persist as a life-long infection. Importantly, there is notable overlap in the pathophysiology between TBI and T. gondii infection, including neuroinflammation. This paper will review current understandings of the clinical problems, pathophysiological mechanisms, and functional outcomes of TBI and T. gondii, before considering the potential synergy between the two conditions. In particular, the discussion will focus on neuroinflammatory processes such as microglial activation, inflammatory cytokines, and peripheral immune cell recruitment that occur during T. gondii infection and after TBI. We will present the notion that these overlapping pathologies in TBI individuals with a chronic T. gondii infection have the strong potential to exacerbate neuroinflammation and related brain damage, leading to amplified functional deficits. The impact of chronic T. gondii infection on TBI should therefore be investigated in both preclinical and clinical studies as the possible interplay could influence treatment strategies.
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- 2020
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37. Ancient MAPK ERK7 is regulated by an unusual inhibitory scaffold required for Toxoplasma apical complex biogenesis.
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Back PS, O'Shaughnessy WJ, Moon AS, Dewangan PS, Hu X, Sha J, Wohlschlegel JA, Bradley PJ, and Reese ML
- Subjects
- Extracellular Signal-Regulated MAP Kinases chemistry, Extracellular Signal-Regulated MAP Kinases genetics, Humans, Phosphorylation, Protein Conformation, Protein Transport, Protozoan Proteins chemistry, Protozoan Proteins genetics, Signal Transduction, Toxoplasmosis metabolism, Toxoplasmosis parasitology, Extracellular Signal-Regulated MAP Kinases metabolism, Fibroblasts parasitology, Organelle Biogenesis, Protozoan Proteins metabolism, Toxoplasma pathogenicity, Toxoplasmosis pathology
- Abstract
Apicomplexan parasites use a specialized cilium structure called the apical complex to organize their secretory organelles and invasion machinery. The apical complex is integrally associated with both the parasite plasma membrane and an intermediate filament cytoskeleton called the inner-membrane complex (IMC). While the apical complex is essential to the parasitic lifestyle, little is known about the regulation of apical complex biogenesis. Here, we identify AC9 (apical cap protein 9), a largely intrinsically disordered component of the Toxoplasma gondii IMC, as essential for apical complex development, and therefore for host cell invasion and egress. Parasites lacking AC9 fail to successfully assemble the tubulin-rich core of their apical complex, called the conoid. We use proximity biotinylation to identify the AC9 interaction network, which includes the kinase extracellular signal-regulated kinase 7 (ERK7). Like AC9, ERK7 is required for apical complex biogenesis. We demonstrate that AC9 directly binds ERK7 through a conserved C-terminal motif and that this interaction is essential for ERK7 localization and function at the apical cap. The crystal structure of the ERK7-AC9 complex reveals that AC9 is not only a scaffold but also inhibits ERK7 through an unusual set of contacts that displaces nucleotide from the kinase active site. ERK7 is an ancient and autoactivating member of the mitogen-activated kinase (MAPK) family and its regulation is poorly understood in all organisms. We propose that AC9 dually regulates ERK7 by scaffolding and concentrating it at its site of action while maintaining it in an "off" state until the specific binding of a true substrate., Competing Interests: The authors declare no competing interest., (Copyright © 2020 the Author(s). Published by PNAS.)
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- 2020
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38. Comparative ex vivo infection with Trypanosoma cruzi and Toxoplasma gondii of human, canine and ovine placenta: Analysis of tissue damage and infection efficiency.
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Liempi A, Castillo C, Medina L, Galanti N, Maya JD, Parraguez VH, and Kemmerling U
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- Animals, Chagas Disease veterinary, Dogs parasitology, Female, Humans, In Vitro Techniques, Pregnancy, Sheep parasitology, Toxoplasma pathogenicity, Trypanosoma cruzi pathogenicity, Chagas Disease pathology, Placenta parasitology, Placenta pathology, Toxoplasmosis pathology, Toxoplasmosis, Animal pathology
- Abstract
Trypanosoma cruzi, the causative agent of Chagas disease, and Toxoplasma gondii, which is responsible for Toxoplasmosis, are two parasites that cause significant protozoan zoonoses and consequently important economic losses in human, companion animals and livestock. For the congenital transmission to occur, both parasites must cross the barrier present in the mammalian placenta, which differs between species. Particularly, hemochorial, endotheliochorial and epitheliochorial placental barriers are present, respectively, in human, dog and sheep. The type of placental barrier has been associated with the probability of transmission of pathogens. In this study, we used experimental placental ex vivo infection models of T. cruzi and T. gondii in the above-mentioned mammals in order to study tissue alterations and to compare infection efficiency. Here, we infected placental term explants from human, dog and sheep and analyzed tissue damage by standard histological and histochemical methods. Comparative infection efficiency was determined by quantitative PCR. Both parasites are able to infect the different placental explants; however, more T. gondii parasites were detected, and T. gondii causes a more severe tissue damage in human and canine explants than T. cruzi. The histopathological changes observed in ovine placenta explants were similar in presence of both parasites. We conclude that the infection efficiency of T. gondii is higher, compared to T. cruzi, during the ex vivo infection of human, canine and ovine placental explants. In addition, the ex vivo infection of mammalian placental explants constitutes an interesting experimental approach to study part of the infection mechanisms as well as host responses during congenital infection of both parasites., Competing Interests: Declaration of Competing Interest None., (Copyright © 2020 Elsevier B.V. All rights reserved.)
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- 2020
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39. Chronic Toxoplasma gondii infection contributes to decreasing of perineuronal nets surrounding neurons in the Corpus striatum of mice.
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de Medeiros Brito RM, da Silva Rodrigues Meurer Y, da Silva Santos L, de Melo Marcelino BM, and de Andrade-Neto VF
- Subjects
- Animals, Chronic Disease, Extracellular Matrix pathology, Female, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Neurons metabolism, Plant Lectins, Receptors, N-Acetylglucosamine, Toxoplasma, Toxoplasmosis metabolism, Corpus Striatum pathology, Neurons pathology, Toxoplasmosis pathology
- Abstract
Recent advances in chronic toxoplasmosis understanding became the focus of discussion about behavioral abnormalities, which could be explained by cyst location and neuronal impairment in specific brain areas. Perineuronal nets (PNNs) are specialized extracellular matrices that surround the neuronal body and proximal dendrites and play key roles in neuronal circuitry maintenance and stabilization. Its impairment can lead to abnormal synaptic functioning with behavioral repercussions. In this context, we analyzed the impact of Toxoplasma gondii infection on neuronal integrity in the Corpus striatum of chronically infected mice. C57BL/6 and Balb/c female mice were infected with T. gondii ME49 cysts. Brain sections were submitted to immunohistochemistry with Wisteria floribunda agglutinin (WFA) for PNN labeling followed by quantification of tissue cyst and labeled neuronal cells 30 days after infection. Our results revealed that C57BL/6 exhibited a significant decrease in PNN-positive (WFA+) labeled neurons and an expressively higher number of tissue cysts than Balb/c mice. It was also possible to observe that the number of T. gondii tissue cysts and the number of WFA+ neurons were inversely correlated for C57BL/6-infected mice. However, no correlation was observed for Balb/c mice. These data suggest how the impact of parasite dissemination in the brain and host characteristics can influence neuronal integrity impairment during infection by decreasing WFA+ neurons. This might be a plausible pathway in which the presence of T. gondii contributes to behavioral changes in the infected host.
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- 2020
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40. Silver Nanoparticle-Induced Apoptosis in ARPE-19 Cells Is Inhibited by Toxoplasma gondii Pre-Infection Through Suppression of NOX4-Dependent ROS Generation.
- Author
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Quan JH, Gao FF, Ismail HAHA, Yuk JM, Cha GH, Chu JQ, and Lee YH
- Subjects
- Animals, Autophagy drug effects, Cell Line, Cell Shape drug effects, Disease Models, Animal, Fibroblasts drug effects, Fibroblasts parasitology, G1 Phase drug effects, Humans, MAP Kinase Signaling System drug effects, Male, Mice, Mitochondria drug effects, Mitochondria metabolism, Models, Biological, Phosphorylation drug effects, Apoptosis drug effects, Metal Nanoparticles chemistry, NADPH Oxidase 4 metabolism, Reactive Oxygen Species metabolism, Retinal Pigment Epithelium metabolism, Retinal Pigment Epithelium parasitology, Silver pharmacology, Toxoplasmosis pathology
- Abstract
Purpose: External and internal stimuli easily affect the retina. Studies have shown that cells infected with Toxoplasma gondii are resistant to multiple inducers of apoptosis. Nanoparticles (NPs) have been widely used in biomedical fields; however, little is known about cytotoxicity caused by NPs in the retina and the modulators that inhibit nanotoxicity., Materials and Methods: ARPE-19 cells from human retinal pigment epithelium were treated with silver nanoparticles (AgNPs) alone or in combination with T. gondii . Then, the cellular toxicity, apoptosis, cell cycle analysis, autophagy, ROS generation, NOX4 expression, and MAPK/mTOR signaling pathways were investigated. To confirm the AgNP-induced cytotoxicity in ARPE-19 cells and its modulatory effects caused by T. gondii infection, the major experiments carried out in ARPE-19 cells were performed again using human foreskin fibroblast (HFF) cells and bone marrow-derived macrophages (BMDMs) from NOX4
-/ - mice., Results: AgNPs dose-dependently induced cytotoxicity and cell death in ARPE-19 cells. Apoptosis, sub-G1 phase cell accumulation, autophagy, JNK phosphorylation, and mitochondrial apoptotic features, such as caspase-3 and PARP cleavages, mitochondrial membrane potential depolarization, and cytochrome c release into the cytosol were observed in AgNP-treated cells. AgNP treatment also increased the Bax, Bik, and Bim protein levels as well as NOX4-dependent ROS generation. However, T. gondii -infected ARPE-19 cells inhibited AgNP-induced apoptosis, JNK phosphorylation, sub-G1 phase cell accumulation, autophagy, NOX4-mediated ROS production, and mitochondrial apoptosis. Furthermore, mitochondrial apoptosis was found in AgNP-treated HFF cells and BMDMs, and AgNP-induced mitochondrial apoptosis inhibition via NOX4-dependent ROS suppression in T. gondii pre-infected HFF cells and BMDMs was also confirmed., Conclusion: AgNPs induced mitochondrial apoptosis in human RPE cells combined with cell cycle dysregulation and autophagy; however, these effects were significantly inhibited by T. gondii pre-infection by suppression of NOX4-mediated ROS production, suggesting that T. gondii is a strong inhibitory modulator of nanotoxicity in in vitro models., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (© 2020 Quan et al.)- Published
- 2020
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41. Toxoplasma GRA15 and GRA24 are important activators of the host innate immune response in the absence of TLR11.
- Author
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Mukhopadhyay D, Arranz-Solís D, and Saeij JPJ
- Subjects
- Animals, Cytokines genetics, Cytokines immunology, Humans, Immunity, Innate genetics, Macrophages parasitology, Macrophages pathology, Mice, Mice, Knockout, RAW 264.7 Cells, Toll-Like Receptors genetics, Toxoplasmosis genetics, Toxoplasmosis pathology, Immunity, Innate immunology, Macrophages immunology, Protozoan Proteins immunology, Toll-Like Receptors immunology, Toxoplasma immunology, Toxoplasmosis immunology
- Abstract
The murine innate immune response against Toxoplasma gondii is predominated by the interaction of TLR11/12 with Toxoplasma profilin. However, mice lacking Tlr11 or humans, who do not have functional TLR11 or TLR12, still elicit a strong innate immune response upon Toxoplasma infection. The parasite factors that determine this immune response are largely unknown. Herein, we investigated two dense granule proteins (GRAs) secreted by Toxoplasma, GRA15 and GRA24, for their role in stimulating the innate immune response in Tlr11-/- mice and in human cells, which naturally lack TLR11/TLR12. Our results show that GRA15 and GRA24 synergistically shape the early immune response and parasite virulence in Tlr11-/- mice, with GRA15 as the predominant effector. Nevertheless, acute virulence in Tlr11-/- mice is still dominated by allelic combinations of ROP18 and ROP5, which are effectors that determine evasion of the immunity-related GTPases. In human macrophages, GRA15 and GRA24 play a major role in the induction of IL12, IL18 and IL1β secretion. We further show that GRA15/GRA24-mediated IL12, IL18 and IL1β secretion activates IFNγ secretion by peripheral blood mononuclear cells (PBMCs), which controls Toxoplasma proliferation. Taken together, our study demonstrates the important role of GRA15 and GRA24 in activating the innate immune response in hosts lacking TLR11., Competing Interests: The authors have declared that no competing interests exist.
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- 2020
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42. Toxoplasma gondii dense granule protein GRA24 drives MyD88-independent p38 MAPK activation, IL-12 production and induction of protective immunity.
- Author
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Mercer HL, Snyder LM, Doherty CM, Fox BA, Bzik DJ, and Denkers EY
- Subjects
- Animals, Enzyme Activation genetics, Enzyme Activation immunology, Interleukin-12 genetics, MAP Kinase Signaling System genetics, Macrophages parasitology, Macrophages pathology, Mice, Mice, Knockout, Myeloid Differentiation Factor 88 genetics, Protozoan Proteins genetics, Toxoplasma genetics, Toxoplasmosis genetics, Toxoplasmosis pathology, p38 Mitogen-Activated Protein Kinases genetics, Interleukin-12 immunology, MAP Kinase Signaling System immunology, Macrophages immunology, Myeloid Differentiation Factor 88 immunology, Protozoan Proteins immunology, Toxoplasma immunology, Toxoplasmosis immunology, p38 Mitogen-Activated Protein Kinases immunology
- Abstract
The apicomplexan Toxoplasma gondii induces strong protective immunity dependent upon recognition by Toll-like receptors (TLR)11 and 12 operating in conjunction with MyD88 in the murine host. However, TLR11 and 12 proteins are not present in humans, inspiring us to investigate MyD88-independent pathways of resistance. Using bicistronic IL-12-YFP reporter mice on MyD88+/+ and MyD88-/- genetic backgrounds, we show that CD11c+MHCII+F4/80- dendritic cells, F4/80+ macrophages, and Ly6G+ neutrophils were the dominant cellular sources of IL-12 in both wild type and MyD88 deficient mice after parasite challenge. Parasite dense granule protein GRA24 induces p38 MAPK activation and subsequent IL-12 production in host macrophages. We show that Toxoplasma triggers an early and late p38 MAPK phosphorylation response in MyD88+/+ and MyD88-/- bone marrow-derived macrophages. Using the uracil auxotrophic Type I T. gondii strain cps1-1, we demonstrate that the late response does not require active parasite proliferation, but strictly depends upon GRA24. By i. p. inoculation with cps1-1 and cps1-1:Δgra24, we identified unique subsets of chemokines and cytokines that were up and downregulated by GRA24. Finally, we demonstrate that cps1-1 triggers a strong host-protective GRA24-dependent Th1 response in the absence of MyD88. Our data identify GRA24 as a major mediator of p38 MAPK activation, IL-12 induction and protective immunity that operates independently of the TLR/MyD88 cascade., Competing Interests: The authors have declared that no competing interests exist.
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- 2020
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43. Screening of compound libraries for inhibitors of Toxoplasma growth and invasion.
- Author
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Han Y, Adeyemi OS, Kabir MHB, and Kato K
- Subjects
- Animals, Cell Differentiation drug effects, Cell Survival drug effects, Flavonoids pharmacology, Humans, Nitriles pharmacology, Pyrimethamine pharmacology, Signal Transduction drug effects, Sulfones pharmacology, Toxoplasma drug effects, Toxoplasma pathogenicity, Toxoplasmosis pathology, Tyrphostins pharmacology, Antiprotozoal Agents pharmacology, Protein Kinase Inhibitors pharmacology, Protein Kinases drug effects, Toxoplasma growth & development, Toxoplasmosis drug therapy
- Abstract
Toxoplasma gondii can infect virtually all warm-blooded animals, including humans. It can differentiate between rapidly replicating tachyzoites that cause acute infection and slowly growing bradyzoites in tissue cysts. Treatment options for toxoplasmosis are challenging because current therapies cannot eradicate the latent T. gondii infection that is mainly caused by the bradyzoite forms. Accordingly, recurrence of infection is a problem for immunocompromised patients and congenitally infected patients. Protein kinases have been widely studied in eukaryotic cells, and while little is known about signaling in Toxoplasma infection, it is likely that protein kinases play a key role in parasite proliferation, differentiation, and probably invasion. To identify optimized new kinase inhibitors for drug development against T. gondii, we screened a library of kinase inhibitor compounds for anti-Toxoplasma activity and host cell cytotoxicity. Pyrimethamine served as a positive control and 0.5% DMSO was used as a negative control. Among the 80 compounds screened, 6 compounds demonstrated ≥ 80% parasite growth inhibition at concentrations at which 5 compounds did not suppress host cell viability, while 3 kinase inhibitors (Bay 11-7082, Tyrphostin AG 1295 and PD-98059) had suppressive effects individually on parasite growth and host cell invasion, but did not strongly induce bradyzoite formation.
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- 2020
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44. ICOS-deficient and ICOS YF mutant mice fail to control Toxoplasma gondii infection of the brain.
- Author
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O'Brien CA and Harris TH
- Subjects
- Animals, Antibodies, Protozoan blood, Brain cytology, Brain immunology, Disease Models, Animal, Forkhead Transcription Factors metabolism, Inducible T-Cell Co-Stimulator Protein deficiency, Inducible T-Cell Co-Stimulator Protein metabolism, Interleukin-2 Receptor alpha Subunit metabolism, Leukocytes, Mononuclear cytology, Mice, Mice, Inbred C57BL, Mice, Knockout, Mutagenesis, Site-Directed, Phosphatidylinositol 3-Kinases metabolism, T-Lymphocytes, Regulatory immunology, T-Lymphocytes, Regulatory metabolism, Toxoplasmosis metabolism, Toxoplasmosis parasitology, Brain metabolism, Inducible T-Cell Co-Stimulator Protein genetics, Toxoplasmosis pathology
- Abstract
Resistance to chronic Toxoplasma gondii infection requires ongoing recruitment of T cells to the brain. Thus, the factors that promote, sustain, and regulate the T cell response to the parasite in the brain are of great interest. The costimulatory molecule ICOS (inducible T cell costimulator) has been reported to act largely through the PI3K pathway in T cells, and can play pro-inflammatory or pro-regulatory roles depending on the inflammatory context and T cell type being studied. During infection with T. gondii, ICOS promotes early T cell responses, while in the chronic stage of infection ICOS plays a regulatory role by limiting T cell responses in the brain. We sought to characterize the role of ICOS signaling through PI3K during chronic infection using two models of ICOS deficiency: total ICOS knockout (KO) mice and ICOS YF mice that are unable to activate PI3K signaling. Overall, ICOS KO and ICOS YF mice had similar severe defects in parasite-specific IgG production and parasite control compared to WT mice. Additionally, we observed expanded effector T cell populations and a loss of Treg frequency in the brains of both ICOS KO and ICOS YF mice. When comparing the remaining Treg populations in infected mice, ICOS KO Tregs expressed WT levels of Foxp3 and CD25, while ICOS YF Tregs expressed significantly less Foxp3 and CD25 compared to both WT and ICOS KO mice. Together, these results suggest that PI3K-independent signaling downstream of ICOS plays an important role in Treg stability in the context of chronic inflammation., Competing Interests: The authors have declared that no competing interests exist.
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- 2020
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45. Treatment with Lycopodium clavatum 200dH Intensifies Kidney and Liver Injury in Mice Infected with Toxoplasma gondii.
- Author
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Pereira AV, Gois MB, Lera KRJL, Miranda-Sapla MM, Falkowski-Temporini GJ, Bezerril JE, Zanusso-Junior G, Ferraz FN, da Silva SS, Aleixo DL, Conchon-Costa I, Sant'Ana DMG, da Costa IN, de Araújo SM, and Pavanelli WR
- Subjects
- Animals, Collagen metabolism, Disease Models, Animal, Fibrosis, Glomerulonephritis metabolism, Glomerulonephritis parasitology, Hepatitis metabolism, Hepatitis parasitology, Male, Mice, Plant Preparations adverse effects, Toxoplasma pathogenicity, Toxoplasmosis pathology, Transforming Growth Factor beta1 metabolism, Glomerulonephritis pathology, Hepatitis pathology, Homeopathy adverse effects, Lycopodium adverse effects, Toxoplasmosis drug therapy
- Abstract
The effects of infection with Toxoplasma gondii vary from asymptomatic to the development of alterations in various organs (including the liver and kidneys) which may be irreversible, and lead to the death of the host. Whereas homeopathy is an alternative and effective method for treating various diseases, including those caused by protozoa, we questioned the effect of using Lycopodium clavatum in mice infected with T. gondii. One hundred male Swiss mice, 60 days old, were divided into four groups (n = 25/group): NIC (uninfected and untreated control), IC (infected and treated with un-dynamized 7% alcohol solution [vehicle]), G48 (infected and treated 48 h before infection and treated three more times; at 2, 4, and 6 days post-infection (dpi) with L. clavatum 200dH), and G72 (infected and treated for 3 consecutive days before infection with L. clavatum 200dH). In this study, physiological, histopathological, and immunological parameters were evaluated. The L. clavatum 200dH intensified renal damage in mice infected with T. gondii from 7 dpi, causing severe and progressive alterations during this period, such as various degrees of inflammation, edema, atrophy, and tubular cystic dilation, degenerated tubules with intra-cytoplasmic vacuoles and coalescing spots, severe vascular lesions, glomerulonephritis, and peri-glomerular congestion. In the G72 animals, which received L. clavatum 200dH, more severe cortex damage was observed (91.66-96.66%) as compared to the IC group (55-80%) and more renal corpuscle, and renal tubule injury was observed (80 ± 5 to 96.7% ± 2.89 of the total area) during all periods, as compared to the IC group (p < 0.05). Both groups presented high liver enzyme levels, and the highest values for AST were observable at 60 dpi. We observed significant increases of type I and III collagen, as well as high levels of TGF-β1 in both organs of the treated animals, the main factor involved in fibrosis in areas damaged by the process. L. clavatum 200dH intensifies kidney and liver alterations in mice infected with T. gondii. Our results reinforce caution when indicating administration schemes and dosages for ultra-diluted drugs.
- Published
- 2020
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46. Characterization of the Role of Amylo-Alpha-1,6-Glucosidase Protein in the Infectivity of Toxoplasma gondii .
- Author
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Cao XZ, Wang JL, Elsheikha HM, Li TT, Sun LX, Liang QL, Zhang ZW, and Lin RQ
- Subjects
- Animals, CRISPR-Cas Systems, Female, Gene Knockdown Techniques, Glycogen Debranching Enzyme System genetics, Mice, Mutation, Protozoan Proteins genetics, Toxoplasma genetics, Toxoplasma ultrastructure, Toxoplasmosis mortality, Toxoplasmosis pathology, Virulence, Glycogen Debranching Enzyme System metabolism, Protozoan Proteins metabolism, Toxoplasma metabolism, Toxoplasmosis parasitology
- Abstract
In this study, we characterized the role of amylo-alpha-1,6-glucosidase (Aa16GL) in the biology and infectivity of Toxoplasma gondii , using Aa16GL-deficient parasites of type I RH and type II Prugniaud (Pru) strains. The subcellular localization of Aa16GL protein was characterized by tagging a 3 × HA to the 3' end of the Aa16GL gene endogenous locus. Immunostaining of the expressed Aa16GL protein revealed that it is located in several small cytoplasmic puncta. Functional characterization of ΔAa16GL mutants using plaque assay, egress assay and intracellular replication assay showed that parasites lacking Aa16GL exhibit a slight reduction in the growth rate, but remained virulent to mice. Although PruΔAa16GL tachyzoites retained the ability to differentiate into bradyzoites in vitro , they exhibited slight reduction in their ability to form cysts in mice. These findings reveal new properties of Aa16GL and suggest that while it does not have a substantial role in mediating T. gondii infectivity, this protein can influence the formation of parasite cysts in mice., (Copyright © 2019 Cao, Wang, Elsheikha, Li, Sun, Liang, Zhang and Lin.)
- Published
- 2019
- Full Text
- View/download PDF
47. Toxoplasma gondii causes lipofuscinosis, collagenopathy and spleen and white pulp atrophy during the acute phase of infection.
- Author
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Pereira AV, Gois MB, Silva MS, Miranda Junior NR, Campos CBHF, Schneider LCL, Barbosa CP, Nogueira-Melo GA, and Sant'Ana DMG
- Subjects
- Animals, Atrophy, Inflammation, Mice, Spleen metabolism, Toxoplasmosis metabolism, Collagen metabolism, Lipofuscin metabolism, Spleen pathology, Toxoplasma, Toxoplasmosis pathology
- Abstract
In this study, we evaluated homeostatic and functional disorders of the spleen in mice inoculated with Toxoplasma gondii. The kinetics of megakaryocyte and leukocyte production, body and spleen mass and certain histopathological aspects were analyzed. There was increased (P < 0.05) the accumulation of lipofuscin in the red pulp of the spleen, in the periods of 30 and 60 dpi of the infection, that is, in the chronification stage of the disease and decrease of the white pulp area. In addition, we observed (from 7dpi) a quantitative and qualitative increase (P < 0.05) in the deposition of collagen fibers in the spleen of all infected mice. Since resolution of the inflammatory process resulted in pathophysiological changes, we can suggest that the T. gondii invaded and multiplied in the cells of the white and red pulps of the spleen. Although we did not find the parasite in the spleen, this hypothesis is supported by the presence of diffuse inflammatory infiltrate, which extended through the spleen parenchyma of all inoculated mice. Taken together, our results suggest that T. gondii causes severe homeostatic disorders that have altered spleen physiology, including diffuse parenchymal inflammation, lipofuscinosis in histiocytes, early aging, collagenopathy, systemic sclerosis and spleen and white pulp atrophy., (© FEMS 2020.)
- Published
- 2019
- Full Text
- View/download PDF
48. The GRA15 protein from Toxoplasma gondii enhances host defense responses by activating the interferon stimulator STING.
- Author
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Wang P, Li S, Zhao Y, Zhang B, Li Y, Liu S, Du H, Cao L, Ou M, Ye X, Li P, Gao X, Wang P, Jing C, Shao F, Yang G, and You F
- Subjects
- Animals, Disease Models, Animal, HEK293 Cells, Humans, Interferon-gamma metabolism, Interleukin-12 Subunit p35 genetics, Interleukin-12 Subunit p35 metabolism, Membrane Proteins deficiency, Membrane Proteins genetics, Mice, Mice, Inbred C57BL, Mice, Knockout, Nucleotidyltransferases deficiency, Nucleotidyltransferases genetics, Protein Multimerization, Protozoan Proteins chemistry, Protozoan Proteins genetics, Spleen metabolism, Survival Rate, Toxoplasma pathogenicity, Toxoplasmosis mortality, Toxoplasmosis parasitology, Toxoplasmosis pathology, Tumor Necrosis Factor Receptor-Associated Peptides and Proteins metabolism, Ubiquitination, Immunity, Innate, Membrane Proteins metabolism, Protozoan Proteins metabolism, Toxoplasma metabolism
- Abstract
Toxoplasma gondii is an important neurotropic pathogen that establishes latent infections in humans that can cause toxoplasmosis in immunocompromised individuals. It replicates inside host cells and has developed several strategies to manipulate host immune responses. However, the cytoplasmic pathogen-sensing pathway that detects T. gondii is not well-characterized. Here, we found that cyclic GMP-AMP synthase (cGAS), a sensor of foreign dsDNA, is required for activation of anti- T. gondii immune signaling in a mouse model. We also found that mice deficient in STING ( Sting
gt/gt mice) are much more susceptible to T. gondii infection than WT mice. Of note, the induction of inflammatory cytokines, type I IFNs, and interferon-stimulated genes in the spleen from Stinggt/gt mice was significantly impaired. Stinggt/gt mice exhibited more severe symptoms than cGAS-deficient mice after T. gondii infection. Interestingly, we found that the dense granule protein GRA15 from T. gondii is secreted into the host cell cytoplasm and then localizes to the endoplasmic reticulum, mediated by the second transmembrane motif in GRA15, which is essential for activating STING and innate immune responses. Mechanistically, GRA15 promoted STING polyubiquitination at Lys-337 and STING oligomerization in a TRAF protein-dependent manner. Accordingly, GRA15-deficient T. gondii failed to elicit robust innate immune responses compared with WT T. gondii. Consequently, GRA15-/- T. gondii was more virulent and caused higher mortality of WT mice but not Stinggt/gt mice upon infection. Together, T. gondii infection triggers cGAS/STING signaling, which is enhanced by GRA15 in a STING- and TRAF-dependent manner., (© 2019 Wang et al.)- Published
- 2019
- Full Text
- View/download PDF
49. The hitchhiker's guide to parasite dissemination.
- Author
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Drewry LL and Sibley LD
- Subjects
- Animals, Blood-Brain Barrier metabolism, Blood-Brain Barrier parasitology, Cell Movement, Central Nervous System Infections immunology, Host-Pathogen Interactions, Humans, Integrins metabolism, Leukocytes metabolism, Toxoplasma genetics, Toxoplasma metabolism, Toxoplasmosis immunology, Toxoplasmosis metabolism, Toxoplasmosis pathology, Transendothelial and Transepithelial Migration, Central Nervous System Infections parasitology, Leukocytes parasitology, Macrophages parasitology, Monocytes parasitology, Toxoplasma pathogenicity, Toxoplasmosis parasitology
- Abstract
Toxoplasma gondii (T. gondii) is a parasitic protist that can infect nearly all nucleated cell types and tissues of warm-blooded vertebrate hosts. T. gondii utilises a unique form of gliding motility to cross cellular barriers, enter tissues, and penetrate host cells, thus enhancing spread within an infected host. However, T. gondii also disseminates by hijacking the migratory abilities of infected leukocytes. Traditionally, this process has been viewed as a route to cross biological barriers such as the blood-brain barrier. Here, we review recent findings that challenge this view by showing that infection of monocytes downregulates the program of transendothelial migration. Instead, infection by T. gondii enhances Rho-dependent interstitial migration of monocytes and macrophages, which enhances dissemination within tissues. Collectively, the available evidence indicates that T. gondii parasites use multiple means to disseminate within the host, including enhanced motility in tissues and translocation across biological barriers., (© 2019 John Wiley & Sons Ltd.)
- Published
- 2019
- Full Text
- View/download PDF
50. A CRISPR platform for targeted in vivo screens identifies Toxoplasma gondii virulence factors in mice.
- Author
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Young J, Dominicus C, Wagener J, Butterworth S, Ye X, Kelly G, Ordan M, Saunders B, Instrell R, Howell M, Stewart A, and Treeck M
- Subjects
- Animals, Cell Line, Clustered Regularly Interspaced Short Palindromic Repeats, Gene Knockout Techniques methods, Gene Library, Genome, Protozoan, Humans, Mice, Inbred C57BL, RNA, Guide, CRISPR-Cas Systems, Toxoplasma pathogenicity, Toxoplasmosis genetics, Toxoplasmosis parasitology, Toxoplasmosis pathology, CRISPR-Cas Systems, Toxoplasma genetics, Virulence Factors genetics
- Abstract
Genome-wide CRISPR screening is a powerful tool to identify genes required under selective conditions. However, the inherent scale of genome-wide libraries can limit their application in experimental settings where cell numbers are restricted, such as in vivo infections or single cell analysis. The use of small scale CRISPR libraries targeting gene subsets circumvents this problem. Here we develop a method for rapid generation of custom guide RNA (gRNA) libraries using arrayed single-stranded oligonucleotides for reproducible pooled cloning of CRISPR/Cas9 libraries. We use this system to generate mutant pools of different sizes in the protozoan parasite Toxoplasma gondi and describe optimised analysis methods for small scale libraries. An in vivo genetic screen in the murine host identifies novel and known virulence factors and we confirm results using cloned knock-out parasites. Our study also reveals a potential trans-rescue of individual knock-out parasites in pools of mutants compared to homogenous knock-out lines of the key virulence factor MYR1.
- Published
- 2019
- Full Text
- View/download PDF
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