19 results on '"Schlindwein AD"'
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2. Comparative study of two extraction methods for enteric virus recovery from sewage sludge by molecular methods
- Author
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Schlindwein, AD, primary, Simões, CMO, additional, and Barardi, CRM, additional
- Published
- 2009
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3. Genotyping and Antiretroviral Drug Resistance Mutations among HIV Patients in Southern Santa Catarina, Brazil.
- Author
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Mendes Marcon CE, Schlindwein AD, de Macedo Brigido LF, Lopez-Lopes GI, Cabral GB, and Schuelter-Trevisol F
- Subjects
- Humans, Brazil epidemiology, Male, Female, Cross-Sectional Studies, Adult, Middle Aged, Antiretroviral Therapy, Highly Active, Viral Load, Mutation, Anti-HIV Agents therapeutic use, Anti-HIV Agents pharmacology, Young Adult, Drug Resistance, Viral genetics, HIV Infections drug therapy, HIV Infections virology, HIV-1 genetics, HIV-1 drug effects, Genotype
- Abstract
Introduction: Therapeutic measures have been successful in increasing survival rates and quality of life of HIV/AIDS-infected people. However, some people fail to respond to antiretroviral therapy (HAART) because of viral resistance-associated mutations., Objective: To identify virus genotype and the presence of mutations that alter the susceptibility to HAART, and factors associated with the occurrence of these mutations., Methods: A cross-sectional study was conducted on adults living with HIV attending a specialized outpatient clinic in southern Santa Catarina, Brazil. The participants were interviewed and had blood samples collected for analysis. Those with detectable viral load were genotyped., Results: Out of the 629 patients recruited, 127 subjects were included due to having a detectable viral load. The most common mutations were M184V and K103N. HIV-1 subtype C was the most prevalent strain. Resistance to HAART was associated with modification in the treatment regimen (p <0.001)., Conclusion: This study concluded that the circulating subtype virus was subtype C and that the mutations K103N and M184V were the most prevalent strains in southern Santa Catarina, Brazil., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)
- Published
- 2024
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4. Longitudinal Assessment of Virological Failure and Antiretroviral Drug Resistance among Treatment-naive Subjects Living with HIV.
- Author
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Mendes Marcon CE, Schlindwein AD, and Schuelter-Trevisol F
- Subjects
- Adult, Humans, Prospective Studies, Quality of Life, Anti-Retroviral Agents pharmacology, Anti-Retroviral Agents therapeutic use, Antiretroviral Therapy, Highly Active, Mutation, Drug Resistance, Viral genetics, Genotype, HIV Infections drug therapy, Anti-HIV Agents pharmacology, Anti-HIV Agents therapeutic use
- Abstract
Introduction: Human immunodeficiency virus (HIV) infection, the etiological agent of acquired immunodeficiency syndrome (AIDS), is a serious public health issue. Therapeutic measures have been successful in increasing the survival and improving the quality of life. However, some treatment-naive subjects living with HIV present resistance-associated mutations as a result of late diagnosis and/or mutant strain infections. The objective of this study was to identify the virus genotype and assess the antiretroviral resistance profile based on the results of HIV genotyping in treatment-naive subjects living with HIV, after six months of taking antiretroviral therapy., Methods: This was a prospective cohort study on treatment-naive adults living with HIV attending a specialized outpatient clinic in southern Santa Catarina State, Brazil. The participants were interviewed and had blood samples drawn. The genotypic antiretroviral drug resistance profile was examined in patients with detectable viral loads., Results: 65 treatment-naive subjects living with HIV were recruited for this study. After six months of taking antiretroviral therapy, resistance-associated mutations were observed in 3 (4.6%) subjects living with HIV., Conclusion: Subtype C was identified as the circulating subtype in southern Santa Catarina State, and L10V, K103N, A98G, and Y179D were the most common mutations found in treatment-naive subjects., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)
- Published
- 2023
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5. Emergence of Two Distinct SARS-CoV-2 Gamma Variants and the Rapid Spread of P.1-like-II SARS-CoV-2 during the Second Wave of COVID-19 in Santa Catarina, Southern Brazil.
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Padilha DA, Benetti Filho V, Moreira RS, Soratto TAT, Maia GA, Christoff AP, Barazzetti FH, Schörner MA, Ferrari FL, Martins CL, Kawagoe EK, Wachter JK, Sachet P, Baptistella AR, Schlindwein AD, Coelho BK, Fernandes SB, Rovaris DB, Debiasi Dos Anjos MP, Melo FR, Bittencourt B, Cunha S, Meneghetti KL, Wendt N, Madaloz TZ, Rodrigues MVD, Souza DSM, Moraes MH, Baptista RP, Toledo-Silva G, Razzera G, Grisard EC, Stoco PH, de Oliveira LFV, Bazzo ML, Fongaro G, and Wagner G
- Subjects
- Brazil epidemiology, Humans, Mutation, Pandemics, Phylogeny, Spike Glycoprotein, Coronavirus genetics, COVID-19 epidemiology, SARS-CoV-2 genetics
- Abstract
The western mesoregion of the state of Santa Catarina (SC), Southern Brazil, was heavily affected as a whole by the COVID-19 pandemic in early 2021. This study aimed to evaluate the dynamics of the SARS-CoV-2 virus spreading patterns in the SC state from March 2020 to April 2021 using genomic surveillance. During this period, there were 23 distinct variants, including Beta and Gamma, among which the Gamma and related lineages were predominant in the second pandemic wave within SC. A regionalization of P.1-like-II in the Western SC region was observed, concomitant to the increase in cases, mortality, and the case fatality rate (CFR) index. This is the first evidence of the regionalization of the SARS-CoV-2 transmission in SC and it highlights the importance of tracking the variants, dispersion, and impact of SARS-CoV-2 on the public health systems.
- Published
- 2022
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6. Maternal and early childhood factors associated with asthma and obesity in children aged 6 to 7 years: a case control study.
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Silva BBD, Silva JD, Traebert JL, and Schlindwein AD
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- Body Mass Index, Case-Control Studies, Child, Child, Preschool, Female, Humans, Overweight, Pregnancy, Risk Factors, Asthma epidemiology, Pediatric Obesity complications, Pediatric Obesity epidemiology
- Abstract
Objective: To determine the maternal and early childhood factors associated with asthma and obesity in children aged 6 to 7 years., Methods: A case-control study conducted with children aged 6 to 7 years. Applications with questions about asthma symptoms in the last 12 months, maternal and childhood data in the first 2 years of life, and anthropometric data were collected. Children who presented asthma symptoms were considered as cases and those without asthma symptoms were considered as controls, later divided into two subgroups that were eutrophic or overweight/obesity. Logistic regression was performed to estimate the association between asthma symptoms (adequate weight and overweight/obesity) and gestational and personal factors, calculating odds ratio and 95% confidence interval (95%CI). Values of p<0.05 were considered significant., Results: Two hundred and one children were evaluated, 25.4% had asthma symptoms, 37.2% of them were overweight/obesity. Waist circumference, triceps skinfold, and body mass index were higher in the group with overweight/obesity asthma symptoms compared to no asthma symptoms (p<0.05). Factors significantly associated with asthma and overweight/obesity symptoms included: the maternal history of asthma (odds ratio of 3.73; 95%CI: 1.10-12.6) and hypertension during pregnancy (odds ratio of 3.29; 95%CI: 1.08-9.94)., Conclusion: Maternal history of asthma and hypertension during pregnancy increased the chances of children, at 6 and 7 years of age, having symptoms of asthma and obesity.
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- 2022
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7. Benzodiazepine deprescription strategies in chronic users: a systematic review.
- Author
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Ribeiro PRS and Schlindwein AD
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- Aged, Benzodiazepines adverse effects, Counseling, Humans, Prospective Studies, Deprescriptions
- Abstract
Background: As long-term use of benzodiazepines increases, adverse effects also become more frequent, especially in elderly adults. Due the potential of causing dependence, poor patient adherence and a lack of awareness of side effects, deprescription is challenging., Objective: This study aimed to identify what are the effective approaches to motivate and promote deprescription of benzodiazepines., Methods: We used MeSH terms to search in five databases that were MEDLINE, Cochrane CENTRAL, LILACS, SCIELO and Science Direct. Then, we selected articles accordingly to inclusion and exclusion criteria. Risk of bias assessment for randomized controlled trials and prospective interventional studies was made using RoB 2.0 and ROBINS-I tools, respectively. For cohort studies, we used the clarity group by McMaster University tool., Results: Database search retrieved 412 results, and 11 studies were selected for analysis. Interventions focusing on patient education to improve community awareness about deprescription presented better discontinuation rates and more potential on motivating discussions about deprescribing with physicians. Interventions based on counselling by different health professionals were not well evaluated as they presented four of six studies as high, serious or critical risk of bias., Conclusions: Although the comparison of different strategies was impaired by the high risk of bias in some studies, patient education focused interventions presented good results. Future studies should consider doing a follow-up of 6 months or longer with evaluation of withdrawal symptoms and sleep patterns, inclusion of young adults on the sample and some form of cognitive evaluation that might influence the results of the intervention., (© The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
- Published
- 2021
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8. Involvement of NLRP3 inflammasome in schizophrenia-like behaviour in young animals after maternal immune activation.
- Author
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Ventura L, Freiberger V, Thiesen VB, Dias P, Dutra ML, Silva BB, Schlindwein AD, and Comim CM
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- Animals, Animals, Newborn metabolism, Behavior Rating Scale standards, Brain metabolism, Female, Gestational Age, Illness Behavior physiology, Immunity, Active drug effects, Inflammasomes immunology, Injections, Intraperitoneal, Lipopolysaccharides administration & dosage, Lipopolysaccharides adverse effects, Male, Mice, Mice, Inbred C57BL, Mothers, Neurocognitive Disorders immunology, Schizophrenia blood, Animals, Newborn psychology, Inflammasomes metabolism, Interleukin-1beta metabolism, NLR Family, Pyrin Domain-Containing 3 Protein metabolism, Schizophrenia diagnosis
- Abstract
Objective: To evaluate the involvement of nod-like receptor pyrin domain-containing protein 3 (NLRP3) inflammasome in schizophrenia-like behaviour in young animals exposed to maternal immune activation (MIA)., Methods: To this aim, on the 15th gestational day, the females received an injection of lipopolysaccharides. When the animals completed 7, 14 and 45 postnatal days, they were killed and the whole brain was dissected for biochemical analysis. Animals with 45 postnatal days were submitted to behavioural tests of locomotor activity, social interaction and stereotyped movements., Results: It was observed that the animals presented schizophrenia-like behaviour at 45 postnatal days associated with the increase of NLRP3 inflammasome expression and IL-1β levels on 7, 14 and 45 postnatal days., Conclusion: This study shows that MIA may be associated with a schizophrenia-like behaviour. This behaviour can be induced to a neuroinflammatory profile in the brain. These evidences may base future studies on the relationship between neuroinflammation and psychiatric disorders.
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- 2020
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9. The first survey of human T-cell lymphotropic viruses (HTLV) in HIV/AIDS patients in Santa Catarina State, Brazil.
- Author
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Marcon CEM, Campos KR, Silva GBD, Schuelter-Trevisol F, Schlindwein AD, Trevisol DJ, and Caterino-de-Araujo A
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- Adolescent, Adult, Aged, Aged, 80 and over, Brazil epidemiology, Cross-Sectional Studies, Epidemiological Monitoring, Female, HIV Infections complications, HTLV-I Infections complications, HTLV-I Infections diagnosis, HTLV-II Infections complications, Humans, Male, Middle Aged, Prevalence, Young Adult, Antibodies, Viral blood, HIV Infections epidemiology, HTLV-I Infections epidemiology, HTLV-II Infections epidemiology, Human T-lymphotropic virus 1 immunology, Human T-lymphotropic virus 2 immunology
- Abstract
Santa Catarina is a Brazilian State that has reported the lowest prevalence of human T-cell lymphotropic viruses (HTLV-1/2) in blood donors (0.04%). Although it presents ports, airports and roads that facilitate the entrance and dissemination of new infectious agents, no information exists concerning the HTLV-1/2 infections in HIV/AIDS patients. This study searched for HTLV-1/2 antibodies in plasma samples of 625 HIV/AIDS patients from the municipality of Tubarao (Southern Santa Catarina), and disclosed 1.1% of positivity (0.48% HTLV-1, 0.48% HTLV-2 and 0.16% untypeable HTLV), and a positive correlation with the male sex (OR 4.16) and intravenous drug use (OR 35.18). Although the percentage of 1.1% appears to be low, it is 27.5 times higher than the percentage detected in blood donors. Since HTLV-1 and HTLV-2 are circulating in HIV-infected individuals in Southern Santa Catarina, and these retroviruses could cause a differently impact on the HIV/AIDS outcomes, the surveillance of HTLV-1/2 is necessary, and it could support public health policies in preventing the transmission and dissemination of these viruses in this State.
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- 2019
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10. Study of the potential adverse effects caused by the dermal application of Dillenia indica L. fruit extract standardized to betulinic acid in rodents.
- Author
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Fernandes FS, da Silva GS, Hilel AS, Carvalho AC, Remor KVT, Schlindwein AD, Kanis LA, Martins DF, and Kviecinski MR
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- Administration, Cutaneous, Animals, Fruit chemistry, Humans, Leukocytes, Mononuclear drug effects, Mice, Pentacyclic Triterpenes, Photosensitizing Agents chemistry, Plant Extracts chemistry, Plant Extracts pharmacology, Rats, Skin Irritancy Tests, Triterpenes chemistry, Triterpenes pharmacology, Betulinic Acid, Clobetasol pharmacology, Dilleniaceae chemistry, Photosensitizing Agents pharmacology, Skin drug effects
- Abstract
This study aimed to evaluate the potential adverse effects of the dermal administration of Dillenia indica Linnaeus (D. indica) fruit extract in healthy rodents; the extract was standardized to betulinic acid. In the initial phase, the acute effects were evaluated on the skin application site of a single extract dose. A skin irritation test was performed in male Wistar rats (n = 8/group) receiving the extract (50-150 mg/mL) with betulinic acid (0.5-1.5%, respectively). A photosensitivity test was performed in male BALB/c mice (n = 6/group) receiving the extract (150 mg/mL). Afterwards, other BALB/c mice (n = 20, male:female, 1:1) were used to assess the systemic alterations caused by 14 daily repeated doses (150 mg/mL) by monitoring the effects on mortality, body morphology, behavior, nutrition status, neuromotor reactions, organ morphology and weight, and blood tests. At this time, 0.5 mg/mL clobetasol was used as the positive control. The skin irritation index suggested that negligible skin irritation had occurred, even when the extract was applied to the rat skin at 150 mg/mL. However, the extract acted as a photosensitizer on mouse skin, showing a photosensitizing activity close to that of 10 mg/mL 5-methoxypsoralen. Repeated doses caused no mouse mortality, aggressiveness, piloerection, diarrhea, convulsions, neuromotor alterations or nutrition status changes. The mouse organ weights did not change, and the mice did not have alterations in their blood compositions. Clobetasol caused a reduction in the mononuclear leukocyte numbers. In general, the data suggest that the extract was safe in healthy rodents but indicate that caution should be taken with the photosensitizing activity; in addition, this activity should be further explored as it may be useful for phototherapeutic drug development., Competing Interests: The authors have declared that no competing interests exist.
- Published
- 2019
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11. Neonatal Immune Activation May Provoke Long-term Depressive Attributes.
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Schelder-Marzzani SH, Dias P, Freiberger V, Ventura L, Silva BB, Dutra ML, Bobinski F, Schlindwein AD, Cassol OJ, and Comim CM
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- Animals, Animals, Newborn, Corticosterone pharmacology, Depression chemically induced, Depression immunology, Depressive Disorder chemically induced, Depressive Disorder drug therapy, Depressive Disorder immunology, Disease Models, Animal, Hippocampus drug effects, Lipopolysaccharides pharmacology, Mice, Inbred C57BL, Depression drug therapy, Hippocampus immunology, Imipramine pharmacology, Time
- Abstract
Background: Studies have shown the relationship between neuroinflammation and depressive- like parameters. However, research still has not been carried out to evaluate neuroinflammation in the neonatal period and psychiatric disorders in adulthood., Objective: To verify the association between neonatal immune activation and depressive-like parameters in adulthood using an animal model., Methods: Two days old C57BL/6 animals were exposed to lipopolysaccharides (LPS) or phosphate- buffered saline (PBS). When the animals were 46 days old, they received PBS or Imipramine at 14 days. At 60 days, the consumption of sucrose; immobility time; adrenal gland and the hippocampus weight; levels of plasma corticosterone and hippocampal Brain-derived neurotrophic factor (BDNF) were evaluated., Results: It was observed that the animals exposed to LPS in the neonatal period and evaluated in adulthood decreased the consumption of sucrose and had reducted hippocampus weight. Also, the exposed animals presented an increase of immobility time, adrenal gland weight and plasma levels of corticosteroids. The use of imipramine did not only modify the decreased hippocampal weight. On the other hand, there were no alterations in the BDNF levels in the hippocampus with or without the use of imipramine., Conclusion: These results suggest that neonatal immune activation may be associated with depressive- like parameters in adulthood. It is believed that endotoxemia may trigger physiological and behavioral alterations, increasing vulnerability for the development of depression in adulthood., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)
- Published
- 2019
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12. Temporal analysis of the relationship between leptospirosis, rainfall levels and seasonality, Santa Catarina, Brazil, 2005-2015.
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Ghizzo Filho J, Nazário NO, Freitas PF, Pinto GA, and Schlindwein AD
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- Brazil epidemiology, Humans, Incidence, Leptospirosis epidemiology, Rain, Seasons
- Abstract
The objective of the study is to analyze the temporal trend of leptospirosis incidence, according to rainfall levels in Santa Catarina, according to seasonality, from 2005 to 2015. This is an ecological study of time series, with date of leptospirosis, rainfall levels and population. The incidence rates of leptospirosis, relative excess of incidence, Pearson's correlation coefficient (r) and an angular coefficient (β) were analyzed from the linear regression adjustment, with a 5% significance level. Distribution of leptospirosis cases, rainfall levels and cases reason/rainfall levels, stratified by month of occurrence were presented. There were 5,274 cases of leptospirosis, with the monthly average being 439 cases, ranging from 211 in September to 770 in January. The mean rate of leptospirosis was 7.03 per 100,000 habitants. The average rainfall level was 158.68 mm, with the lowest levels occurring in August, average of 124.9 mm, and the highest in January average of 213.20 mm. The positive correlation between leptospirosis rates and rainfall levels, during the period from January to December (r = 0.68, p = 0.023), indicates a positive temporal association between the amount of rainfall and the cases of the disease. The disease occurred all year round and presented a distinct seasonality from October to March.
- Published
- 2018
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13. Isoniazid-induced control of Mycobacterium tuberculosis by primary human cells requires interleukin-1 receptor and tumor necrosis factor.
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Yamashiro LH, Eto C, Soncini M, Horewicz V, Garcia M, Schlindwein AD, Grisard EC, Rovaris DB, and Báfica A
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- Bacterial Proteins metabolism, Cells, Cultured, Humans, Macrophages metabolism, Monocytes metabolism, Phosphatidylinositol 3-Kinases immunology, Receptors, Interleukin-1 antagonists & inhibitors, Tuberculosis drug therapy, Tuberculosis immunology, Tumor Necrosis Factor-alpha antagonists & inhibitors, Antitubercular Agents pharmacology, Interleukin-1beta immunology, Isoniazid pharmacology, Mycobacterium tuberculosis drug effects, Receptors, Interleukin-1 immunology, Tumor Necrosis Factor-alpha immunology
- Abstract
Proinflammatory cytokines are critical mediators that control Mycobacterium tuberculosis (Mtb) growth during active tuberculosis (ATB). To further inhibit bacterial proliferation in diseased individuals, drug inhibitors of cell wall synthesis such as isoniazid (INH) are employed. However, whether INH presents an indirect effect on bacterial growth by regulating host cytokines during ATB is not well known. To examine this hypothesis, we used an in vitro human granuloma system generated with primary leukocytes from healthy donors adapted to model ATB. Intense Mtb proliferation in cell cultures was associated with monocyte/macrophage activation and secretion of IL-1β and TNF. Treatment with INH significantly reduced Mtb survival, but altered neither T-cell-mediated Mtb killing, nor production of IL-1β and TNF. However, blockade of both IL-1R1 and TNF signaling rescued INH-induced killing, suggesting synergistic roles of these cytokines in mediating control of Mtb proliferation. Additionally, mycobacterial killing by INH was highly dependent upon drug activation by the pathogen catalase-peroxidase KatG and involved a host PI3K-dependent pathway. Finally, experiments using coinfected (KatG-mutated and H37Rv strains) cells suggested that active INH does not directly enhance host-mediated killing of Mtb. Our results thus indicate that Mtb-stimulated host IL-1 and TNF have potential roles in TB chemotherapy., (© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)
- Published
- 2016
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14. Mycobacteria mobility shift assay: a method for the rapid identification of Mycobacterium tuberculosis and nontuberculous mycobacteria.
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Wildner LM, Bazzo ML, Liedke SC, Nogueira CL, Segat G, Senna SG, Schlindwein AD, Oliveira JG, Rovaris DB, Bonjardim CA, Kroon EG, and Ferreira PC
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- Bacterial Proteins genetics, Bacterial Typing Techniques, DNA, Bacterial genetics, Humans, Mycobacterium Infections microbiology, Mycobacterium Infections, Nontuberculous microbiology, Mycobacterium tuberculosis classification, Nontuberculous Mycobacteria classification, Polymerase Chain Reaction, Electrophoretic Mobility Shift Assay, Mycobacterium tuberculosis isolation & purification, Nontuberculous Mycobacteria isolation & purification, RNA, Ribosomal, 16S genetics
- Abstract
The identification of mycobacteria is essential because tuberculosis (TB) and mycobacteriosis are clinically indistinguishable and require different therapeutic regimens. The traditional phenotypic method is time consuming and may last up to 60 days. Indeed, rapid, affordable, specific and easy-to-perform identification methods are needed. We have previously described a polymerase chain reaction-based method called a mycobacteria mobility shift assay (MMSA) that was designed for Mycobacterium tuberculosis complex (MTC) and nontuberculous mycobacteria (NTM) species identification. The aim of this study was to assess the MMSA for the identification of MTC and NTM clinical isolates and to compare its performance with that of the PRA-hsp65 method. A total of 204 clinical isolates (102 NTM and 102 MTC) were identified by the MMSA and PRA-hsp65. For isolates for which these methods gave discordant results, definitive species identification was obtained by sequencing fragments of the 16S rRNA and hsp65 genes. Both methods correctly identified all MTC isolates. Among the NTM isolates, the MMSA alone assigned 94 (92.2%) to a complex or species, whereas the PRA-hsp65 method assigned 100% to a species. A 91.5% agreement was observed for the 94 NTM isolates identified by both methods. The MMSA provided correct identification for 96.8% of the NTM isolates compared with 94.7% for PRA-hsp65. The MMSA is a suitable auxiliary method for routine use for the rapid identification of mycobacteria.
- Published
- 2014
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15. Immunological responses of the mangrove oysters Crassostrea gasar naturally infected by Perkinsus sp. in the Mamanguape Estuary, Paraíba state (Northeastern, Brazil).
- Author
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Queiroga FR, Marques-Santos LF, Hégaret H, Soudant P, Farias ND, Schlindwein AD, and Mirella da Silva P
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- Animals, Aquaculture, Brazil, Estuaries, Flow Cytometry veterinary, Hemocytes cytology, Hemocytes metabolism, Phagocytosis, Reactive Oxygen Species metabolism, Seasons, Alveolata physiology, Crassostrea immunology, Crassostrea microbiology
- Abstract
Perkinsus genus includes protozoan parasites of marine mollusks, especially bivalves. In the last four years, this parasite has been detected in mangrove oysters Crassostrea rhizophorae and Crassostrea gasar from the Northeastern region of Brazil. Hemocytes are the key cells of the oyster immune system, being responsible for a variety of cellular and humoral reactions, such as phagocytosis, encapsulation and the release of several effector molecules that control the invasion and proliferation of microorganisms. In Brazil, there is little information on perkinsosis and none on the immune responses of native oysters' species against Perkinsus spp. The objective of this study was to determine the effects of natural infection by Perkinsus sp. on the immunological parameters of mangrove oysters C. gasar cultured in the Mamanguape River Estuary (Paraíba, Brazil). Adults oysters (N = 40/month) were sampled in December 2011, March, May, August and October 2012. Gills were removed and used to determine the presence and intensity of the Perkinsus sp. infection, according to a scale of four levels (1-4), using the Ray's fluid thioglycollate medium assay. Immunological parameters were measured in hemolymph samples by flow cytometry, including: total hemocyte count (THC), differential hemocyte count (DHC), cell mortality, phagocytic capacity, and production of Reactive Oxygen Species (ROS). The plasma was used to determine the hemagglutination activity. The results showed the occurrence of Perkinsus sp. with the highest mean prevalence (93.3%) seen so far in oyster populations in Brazil. Despite that, no oyster mortality was associated. In contrast, we observed an increase in hemocyte mortality and a suppression of two of the main defense mechanisms, phagocytosis and ROS production in infected oysters. The increase in the percentage of blast-like cells on the hemolymph, and the increase in THC in oysters heavily infected (at the maximum intensity, 4) suggest an induction of hemocytes proliferation. The immunological parameters varied over the studied months, which may be attributed to the dynamics of infection by Perkinsus sp. The results of the present study demonstrate that Perkinsus sp. has a deleterious effect on C. gasar immune system, mainly in high intensities, which likely renders oysters more susceptible to other pathogens and diseases., (Copyright © 2013 Elsevier Ltd. All rights reserved.)
- Published
- 2013
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16. The genome of Anopheles darlingi, the main neotropical malaria vector.
- Author
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Marinotti O, Cerqueira GC, de Almeida LG, Ferro MI, Loreto EL, Zaha A, Teixeira SM, Wespiser AR, Almeida E Silva A, Schlindwein AD, Pacheco AC, Silva AL, Graveley BR, Walenz BP, Lima Bde A, Ribeiro CA, Nunes-Silva CG, de Carvalho CR, Soares CM, de Menezes CB, Matiolli C, Caffrey D, Araújo DA, de Oliveira DM, Golenbock D, Grisard EC, Fantinatti-Garboggini F, de Carvalho FM, Barcellos FG, Prosdocimi F, May G, Azevedo Junior GM, Guimarães GM, Goldman GH, Padilha IQ, Batista Jda S, Ferro JA, Ribeiro JM, Fietto JL, Dabbas KM, Cerdeira L, Agnez-Lima LF, Brocchi M, de Carvalho MO, Teixeira Mde M, Diniz Maia Mde M, Goldman MH, Cruz Schneider MP, Felipe MS, Hungria M, Nicolás MF, Pereira M, Montes MA, Cantão ME, Vincentz M, Rafael MS, Silverman N, Stoco PH, Souza RC, Vicentini R, Gazzinelli RT, Neves Rde O, Silva R, Astolfi-Filho S, Maciel TE, Urményi TP, Tadei WP, Camargo EP, and de Vasconcelos AT
- Subjects
- Animals, Anopheles classification, Brazil, Chromosomes, Insect genetics, DNA Transposable Elements, Evolution, Molecular, Female, Genetic Variation, Host-Parasite Interactions, Insect Proteins genetics, Insect Vectors classification, Insecticide Resistance, Insecticides pharmacology, Malaria parasitology, Male, Molecular Sequence Annotation, Phylogeny, Synteny, Transcriptome, Anopheles genetics, Genome, Insect, Insect Vectors genetics
- Abstract
Anopheles darlingi is the principal neotropical malaria vector, responsible for more than a million cases of malaria per year on the American continent. Anopheles darlingi diverged from the African and Asian malaria vectors ∼100 million years ago (mya) and successfully adapted to the New World environment. Here we present an annotated reference A. darlingi genome, sequenced from a wild population of males and females collected in the Brazilian Amazon. A total of 10 481 predicted protein-coding genes were annotated, 72% of which have their closest counterpart in Anopheles gambiae and 21% have highest similarity with other mosquito species. In spite of a long period of divergent evolution, conserved gene synteny was observed between A. darlingi and A. gambiae. More than 10 million single nucleotide polymorphisms and short indels with potential use as genetic markers were identified. Transposable elements correspond to 2.3% of the A. darlingi genome. Genes associated with hematophagy, immunity and insecticide resistance, directly involved in vector-human and vector-parasite interactions, were identified and discussed. This study represents the first effort to sequence the genome of a neotropical malaria vector, and opens a new window through which we can contemplate the evolutionary history of anopheline mosquitoes. It also provides valuable information that may lead to novel strategies to reduce malaria transmission on the South American continent. The A. darlingi genome is accessible at www.labinfo.lncc.br/index.php/anopheles-darlingi.
- Published
- 2013
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17. The Trypanosoma rangeli trypomastigote surfaceome reveals novel proteins and targets for specific diagnosis.
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Wagner G, Eiko Yamanaka L, Moura H, Denardin Lückemeyer D, Schlindwein AD, Hermes Stoco P, Bunselmeyer Ferreira H, Robert Barr J, Steindel M, and Grisard EC
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- Animals, Humans, Mice, Serologic Tests methods, Trypanosomiasis diagnosis, Proteomics, Protozoan Proteins metabolism, Trypanosoma rangeli metabolism, Trypanosomiasis metabolism
- Abstract
Sympatric distribution and sharing of hosts and antigens by Trypanosoma rangeli and Trypanosoma cruzi, the etiological agent of Chagas' disease, often incur in misdiagnosis and improper epidemiological inferences. Many secreted and surface proteins (SP) have been described as important antigens shared by these species. This work describes the T. rangeli surfaceome obtained by gel-free (LC-ESI-MS/MS) and gel-based (GeLC-ESI-MS/MS) proteomic approaches, and immunoblotting analyses and the comparison of these SP with T. cruzi. A total of 138 T. rangeli proteins and 343 T. cruzi proteins were obtained, among which, 42 and 157 proteins were exclusively identified in T. rangeli or T. cruzi trypomastigotes, respectively. Immunoblotting assays using sera from experimentally infected mice revealed a distinct band pattern for each species. MS/MS analysis of T. rangeli exclusive bands revealed two unique GP63-related proteins and flagellar calcium-binding protein. Also, a ~32kDa band composed of 12 distinct proteins was exclusively recognized by anti-T. cruzi serum. This highly sensitive proteomic assessment of surface proteins characterized the T. rangeli surfaceome, revealing several differences and similarities between these two parasites. The study reports new T. rangeli-specific proteins with promising use in differential diagnosis from T. cruzi., Biological Significance: In this manuscript, we report the first proteomic analysis of the T. rangeli surface (surfaceome), a non-pathogenic parasite occurring in sympatry with T. cruzi, the etiological agent of Chagas disease. This comparative proteomic analysis was performed using high-throughput in-gel and gel-free proteomic approaches combined with immunoblotting, allowing us to identify new T. rangeli-specific proteins with promising use in differential serodiagnosis, among several other protein not previously reported for this taxon. Additionally, cross-recognition assays showed that T. cruzi surface proteins were recognized by heterologous serum (anti-T. rangeli) that strengthens the possibility of misdiagnosis of Chagas disease in humans and other mammals. Thus, this work provides new insights to understand the serological cross-reactivity between T. cruzi and T. rangeli, as well as, the identification of targets for specific T. rangeli diagnosis as revealed by the comparative surfaceome analysis. We strongly believe that this research is of importance to the readers of Journal of Proteomics since it provides new potential markers for diagnosis of both T. cruzi and T. rangeli parasites increasing the spectrum of specific targets for unambiguous diagnosis of T. rangeli and T. cruzi infections, besides describing new approaches to assess the trypanosomatids proteome., (Copyright © 2013 Elsevier B.V. All rights reserved.)
- Published
- 2013
- Full Text
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18. Identification of differentially transcribed genes in shrimp Litopenaeus vannamei exposed to osmotic stress and challenged with WSSV virus.
- Author
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Gonçalves-Soares D, Seiffert WQ, Schlindwein AD, Toledo-Silva G, Zanette J, Marques MR, and Bainy AC
- Subjects
- Animals, Gene Expression Profiling, Gene Expression Regulation, Host-Pathogen Interactions, Osmotic Pressure, Penaeidae physiology, Penaeidae genetics, Penaeidae virology, White spot syndrome virus 1 physiology
- Abstract
The effects of hyposmotic stress and white spot syndrome virus (WSSV) challenge in expression was studied in the marine shrimp Litopenaeus vannamei. Messenger RNA from gills of shrimp submitted to osmotic stress was isolated to identify genes differentially expressed through the suppressive subtractive hybridization (SSH) method. Two subtractive libraries forward and two reverse were constructed to identify up and down-regulated genes under these conditions. About 192 clones were sequenced, of which 46 genes were identified. These genes encode proteins corresponding to a wide range of biological roles, including defense, cell signaling, electron transfer, cell proliferation and differentiation, apoptosis, intermediary metabolism, cytoskeleton and digestion. Among the identified genes, 19 were up-regulated and 27 were down-regulated in the animals kept at a lower ion concentration. We evaluated the expression of eight genes by RT-qPCR in shrimp submitted to hyposmotic conditions with and without WSSV challenge. The SSH enabled the identification of genes that are influenced by hyposmotic stress. A significant up-regulation was observed in lectin-C, QM, TGF beta inducible nuclear protein 1, ciclophilin, malate dehydrogenase, mitochondrial ATP synthase F chain and ATP synthase subunit 9 precursor transcripts. However, the expression of these genes in L. vannamei was not affected by WSSV infection both at isosmotic and hyposmotic conditions., (Copyright © 2011 Elsevier Inc. All rights reserved.)
- Published
- 2012
- Full Text
- View/download PDF
19. Detection of enteric viruses in sewage sludge and treated wastewater effluent.
- Author
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Schlindwein AD, Rigotto C, Simões CM, and Barardi CR
- Subjects
- Animals, Brazil, Cell Line, DNA, Viral isolation & purification, Humans, RNA, Viral isolation & purification, Seasons, Time Factors, Polymerase Chain Reaction methods, Sewage virology, Viruses isolation & purification, Waste Disposal, Fluid methods, Water Microbiology
- Abstract
Sewage sludge and treated wastewater when contaminated with enteric virus and discharged into the environment, could pose a human health risk. The aim of study was to verify the presence and viability of enteric viruses in sewage sludge and treated wastewater at a local sewage plant in Florianopolis city, Brazil. Sewage sludge was concentrated by organic flocculation and polyethylene glycol precipitation and wastewater by electronegative membrane filtration and ultrafiltration by Centriprep Concentrator. Adenovirus (AdV), hepatitis A virus (HAV), and Rotavirus (RV) were examined for all samples for 12 months and Poliovirus (PV) was also tested for in sewage sludge samples. AdV was the most prevalent in both kind of samples, followed by RV, PV (in sludge) and HAV. Viral viability by cell culture (ICC-PCR) was: AdV: 100%, HAV: 16.7%, PV: 91.7%, RV: 25% in sludge and AdV: 66.6%, HAV: 66.6% and RV: 0% in wastewater. IFA for AdV in sludge ranged from 70 to 300 FFU/ml. QPCR for AdV ranged from 4.6 x 10(4) to 1.2 x 10(6) and from 50 to 1.3 x 10(4) gc/ml in sludge and wastewater, respectively. HAV quantification in sludge ranged from 3.1 x 10(2) to 5.4 x 10(2) gc/ml. In conclusion, it was possible to correlate presence and viability of enteric viruses in the environmental samples analyzed.
- Published
- 2010
- Full Text
- View/download PDF
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