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Objectives: This study was conducted to determine the efficacy of mesenchymal stem cells (MSCs) or low-dose gamma radiation (LDR) on liver injury compared to the effect of olive leaf extract as a hepatoprotective agent. Methods: Rats were allocated into six groups; group I served as the negative control. Group II received 5% dextran sodium sulfate (DSS) in its drinking water for 1 week. Group III was injected with a single dose of 1 × 106 bone marrow-derived mesenchymal stem cells (BM-MSCs) intravenously. Group IV was treated as in group III after 5% DSS treatment. Group V was given 5% DSS, followed by olive leaf extract (OLE) (1000 mg/ kg, oral). Group VI: 5% DSS for 1 week, then was exposed to low-dose gamma radiation (LDR) (0.05 Gy). Results: Rats treated with OLE, BM-MSCs, or exposed to LDR exerted significant alleviation in all hepatic biomarkers, significant enhancements in oxidative stress parameters, and improvements in inflammatory biomarkers Interleukin-1 beta (IL-1β) and Interferon gamma (INF-γ) hepatic contents compared with those of the DSS group. Histological pictures emphasized the biochemical findings. Conclusions: BM-MSCs might be a valuable therapeutic approach to overcome hepatic injury. Exposure to LDR provided protective mechanisms that allow the body to survive better. [ABSTRACT FROM AUTHOR]

This study proposed that sodium selenite (SSe) could counteract the inflammatory signaling allied with radiation-induced testicular damage. Mature male Sprague-Dawley rats were exposed to a single-dose γ–radiation (5 Gy) and treated with sodium selenite (SSe) daily for nine days. According to the findings, SSe significantly preserved spermatogenesis activity, reducing the levels of the p-STAT3 protein, NF-кB and IL-1, as well as the relative expression of the Nrf2 protein, antioxidant activity, and serum testosterone in irradiated (IRR) rats. In light of this, we can state that, through targeting the Nrf2/STAT3 pathway, SSe may be able to reduce oxidative damage in the testes of radiation-toxicity rats because of its antioxidant characteristics. Thus, the antioxidant properties of SSe offer a novel method for discovering medicines that can be used in radioprotector clinical trials. [ABSTRACT FROM AUTHOR]

The goal of this study was to assess the influence of bone marrow‐derived mesenchymal stem cells (BM‐MSCs) on the nephrotoxicity induced by fractionated doses of gamma irradiation (Rad) and the cotherapy of levetiracetam and oxcarbazepine in male rats. Adult rats were randomly divided into four groups. Group I: Control, Group II: antiepileptic drugs (AEDs), Group III: AEDs +Rad and Group IV: AEDs + Rad + MSCs. Rats treated with AEDs and exposed to fractionated doses of γ‐irradiation displayed a discernible increase in serum urea, creatinine, kidney injury marker, kidney malondialdehyde, transforming growth factor beta (TGF‐β) and the relative expression of Smad3 along with a decrease in the relative expression of Smad7 and glutathione level. Alternatively, groups treated with BM‐MSCs with AEDs and Rad showed a substantial modification in the majority of the evaluated parameters and looked to be successful in reducing the hazards of the combination therapy of AEDs and radiation. The reno‐histopathological study supports the biochemical analysis. In conclusion, BM‐MSCs exhibited therapeutic potential against nephrotoxicity induced by fractionated doses of γ‐irradiation and AEDs. The outcome was brought about by the downregulation of the TGF‐β/Smad pathway. BM‐MSCs might be suggested as a valuable therapeutic strategy to overcome kidney injury induced by gamma irradiation during AEDs cotherapy. Significance statement: This work concerns the effect of stem cell treatment to eliminate the renal injury induced by gamma irradiation during antiepileptic drug cotherapy. [ABSTRACT FROM AUTHOR]

Organisms frequently suffer negative effects from large doses of ionizing radiation. However, radiation is not as hazardous at lower doses as was once believed. The current study aims to evaluate the possible radio‐adaptive effect induced by low‐dose radiation (LDR) in modulating high‐dose radiation (HDR) and N‐nitrosodiethylamine (NDEA)‐induced lung injury in male albino rats. Sixty‐four male rats were randomly divided into four groups: Group 1 (control): normal rats; Group 2 (D): rats given NDEA in drinking water; Group 3 (DR): rats administered with NDEA then exposed to fractionated HDR; and Group 4 (DRL): rats administered with NDEA then exposed to LDR + HDR. In the next stage, malondialdehyde (MDA), glutathione reduced (GSH), catalase (CAT), and superoxide dismutase (SOD) levels in the lung tissues were measured. Furthermore, the enzyme‐linked immunoassay analysis technique was performed to assess the Toll‐like receptor 4 (TLR4), interleukin‐1 receptor‐associated kinase 4 (IRAK4), and mitogen‐activated protein kinases (MAPK) expression levels. Histopathological and DNA fragmentation analyses in lung tissue, in addition to hematological and apoptosis analyses of the blood samples, were also conducted. Results demonstrated a significant increase in antioxidant defense and a reduction in MDA levels were observed in LDR‐treated animals compared to the D and DR groups. Additionally, exposure to LDR decreased TLR4, IRAK4, and MAPK levels, decreased apoptosis, and restored all the alterations in the histopathological, hematological parameters, and DNA fragmentation, indicating its protective effects on the lung when compared with untreated rats. Taken together, LDR shows protective action against the negative effects of subsequent HDR and NDEA. This impact may be attributable to the adaptive response induced by LDR, which decreases DNA damage in lung tissue and activates the antioxidative, antiapoptotic, and anti‐inflammatory systems in the affected animals, enabling them to withstand the following HDR exposure. Significance statement: The present work was designed to evaluate the adaptive response of low doses of gamma radiation against high doses of gamma radiation‐induced toxicity in lung tissue. [ABSTRACT FROM AUTHOR]

The current study was designed to investigate the protective effect of kefir milk on ethanol-induced gastric ulcers in γ-irradiated rats. The results of the present study revealed that treatment with γ-irradiation and/or ethanol showed a significant increase in ulcers number, total acidity, peptic, H + K + ATPase, MMP-2 and MMP-9 activities and MDA level, which were accompanied by a significant decrease in the mucus content, the stomach GSH level, the GSH-Px activity and DNA damage. Pre-treatment with kefir milk exert significant improvement in all the tested parameters. Kefir milk exerts comparable effect to that of the antiulcer drug ranitidine. In conclusion, the present study revealed that oral administration of kefir milk prevents ethanol-induced gastric ulcer in γ-irradiated rats that could attribute to its antioxidant, anti-apoptotic and radio-protective activities. [ABSTRACT FROM AUTHOR]

• PVDF and PVDF@CNCs membranes nanofiber were developed. • PVDF shows higher piezoelectric effect than PVDF@CNCs membrane. • PVDF@CNCs membrane shows the highest water flux and oil rejection in oil/water separation. In this communication, we report a smart membrane for both energy harvesting and oil/water separation application. The membrane was manufactured from polyvinylidene fluoride (PVDF) nanofiber blended with cellulose nanocrystals (CNCs) as a sustainable material. A promising result in energy harvesting from the cyclic load effect and in oil/water separation was achieved. The developed membranes were characterized for their morphology, functional group, and surface properties using transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and water contact angle (WCA), respectivley. The membrane shows piezoelectric response result about 3.5 V and 10 nA corresponding to PVDF membrane comparing to PVDF@CNCs membrane. However, in oil/water separation application, PVDF@CNCs shows higher water flux (85646.43 ml/m2.h) comparing to pristine PVDF membrane (73589.29 ml/m2.h). These resulted membranes are promising in oily wastewater separation and in the application of powering sensors that capable of measuring water quality after separation and treatment process. [ABSTRACT FROM AUTHOR]

This study suggested that methylseleninic acid (MSA) could respond to the inflammatory signaling associated with ionizing radiation-induced testicular damage. Mature male rats were divided into four groups: negative control, whole body γ-irradiated (IRR) (5 Gy), MSA (0.5 mg/kg, daily for nine consecutive days), and MSA+ IRR groups. MSA increased serum testosterone level and testicular glutathione peroxidase (GPx) as well as decreased the percentage of sperm abnormalities. Radiation prompted inflammatory signaling in the testes through increasing phospho-janus kinase1 (p-JAK1), phospho-signal transducers and activators of transcription 3 (p-STAT3) protein expressions. This induced increment in the inflammatory markers including nuclear factor- kappa B (NF-κB) and interleukin-1beta (IL-1β) levels. Also, radiation induced elevation of nitric oxide (NO) and malondialdhyde (MDA) levels with consequent reduction in testicular reduced glutathione level (GSH) and superoxide dismutase (SOD) activity. MSA significantly counteracted the radiation effect on testicular nuclear factor erythroid-2-related factor-2 (Nrf2) and suppressor of cytokine signaling (Socs3) protein expressions. In summary, this investigation proposed that MSA preserved spermatogenesis through increasing testosterone levels and GPx activity. Additionally, it diminished testicular inflammation by increasing of Nrf2 and Socs3 levels leading to reducing of p-JAK1, p-STAT3 and NF-κB levels. Histopathological examination results of testicular tissues showed a coincidence with the biochemical analysis. [ABSTRACT FROM AUTHOR]

Background: Minced meat is a valuable source of nutrients, but it is vulnerable to contamination by microorganisms commonly present in the environment. In addition, there is a risk of adulteration with cheaper meat sources, which can be harmful to consumers. Aim: It is crucial to identify meat adulteration with distinct microbiological analysis for legal, economic, religious, and public health purposes. Methods: A total of 100 minced meat samples were collected from several markets in Sharkia Governorate, Egypt. These samples were then subjected to bacteriological testing and an advanced multiplex PCR method. This method enables the detection of bovine, equine, porcine, and dog species in meat samples with just one step. Results: The adulterated samples had a higher total bacterial count and pH values compared to pure bovine meat. These differences in bacterial count and pH values were statistically significant, with p-values of 0.843 (log10) and 0.233, respectively. The frequency of Escherichia coli occurrence was 13%, and the O111 serotype was predominant in the adulterated samples. Listeria monocytogenes and Staphylococcus aureus were isolated with prevalence rates of 3% and 29%, respectively. Besides, the SYBR-green multiplex real-time PCR assay used in this study detected adulteration with dog, equine, and porcine meats in the examined samples at rates of 9%, 5%, and 4%, respectively. Conclusion: This method provides a sensitive and specific approach to detect issues related to well-being and safety. [ABSTRACT FROM AUTHOR]

Background and Aim: Given the rise in stray and imported dogs in Egypt over the past 5 years, it is surprising that no report of Brucella canis infection in dogs or humans has been documented in Egypt's published papers. This study aimed to detect the presence of antibodies against the rough (B. canis) and smooth Brucellae among dogs in Egypt and to characterize the Brucella species circulating in dogs. Materials and Methods: Blood samples (n = 449) were collected from owned and stray dogs in the Greater Cairo region (n = 309) and Damietta governorate (n = 140). The apparent, true, and total seroprevalence of canine brucellosis caused by B. canis infection were calculated using the 2-mercaptoethanol tube agglutination test (2-ME TAT) and rapid slide agglutination test (RSAT). We used the rose Bengal test (RBT) and the buffered acidified plate antigen test (BAPAT) to check the serum samples from dogs for the presence of antibodies against smooth Brucellae. Three polymerase chain reaction (PCR) assays - Bruce-ladder PCR, B. canis species-specific PCR (BcSS-PCR), and Abortus Melitensis Ovis Suis (AMOS)-PCR - were used to determine the Brucella species in the buffy coats of the serologically positive dogs. Results: The overall apparent and true prevalence of B. canis infection in dogs were estimated to be 3.8% and 13.2%. The estimated true prevalence in stray dogs (15%) was higher than in owned dogs (12.5%). The BAPAT and the RBT using smooth antigens revealed that 11 (2.4%) and 9 (2%) were positive. Bruce-ladder PCR targeting eryC, ABC, and Polysaccharide deacetylase genes was able to identify B. canis in nine out of 17 buffy coat samples. AMOS-PCR identified the eight undetermined Brucella species by Bruce-ladder PCR as Brucella abortus (n = 4) and Brucella melitensis (n = 4). To exclude the presence of Brucella suis, a one-step species-specific BcSS-PCR was performed and specifically amplified all B. canis DNA (n = 9) the same as did the Bruce-ladder PCR. Conclusion: To the best of our knowledge, this is the first report of B. canis detection in dogs in Egypt. Molecular identification of B. abortus and B. melitensis in the Egyptian canines highlights the role of stray dogs in brucellosis remerging in Brucellosis-free dairy farms. Brucella canis infection can be diagnosed specifically with the one-step BcSS-PCR. The obtained results set-an-alarm to the veterinary authorities to launch plans to control this disease in dogs. [ABSTRACT FROM AUTHOR]

Due to the huge number of connected Internet of Things (IoT) devices within a network, denial of service and flooding attacks on networks are on the rise. IoT devices are disrupted and denied service because of these attacks. In this study, we proposed a novel hybrid meta-heuristic adaptive particle swarm optimization–whale optimizer algorithm (APSO-WOA) for optimization of the hyperparameters of a convolutional neural network (APSO-WOA-CNN). The APSO–WOA optimization algorithm's fitness value is defined as the validation set's cross-entropy loss function during CNN model training. In this study, we compare our optimization algorithm with other optimization algorithms, such as the APSO algorithm, for optimization of the hyperparameters of CNN. In model training, the APSO–WOA–CNN algorithm achieved the best performance compared to the FNN algorithm, which used manual parameter settings. We evaluated the APSO–WOA–CNN algorithm against APSO–CNN, SVM, and FNN. The simulation results suggest that APSO–WOA–CNf[N is effective and can reliably detect multi-type IoT network attacks. The results show that the APSO–WOA–CNN algorithm improves accuracy by 1.25%, average precision by 1%, the kappa coefficient by 11%, Hamming loss by 1.2%, and the Jaccard similarity coefficient by 2%, as compared to the APSO–CNN algorithm, and the APSO–CNN algorithm achieves the best performance, as compared to other algorithms. [ABSTRACT FROM AUTHOR]

Biofilm-producing ability has been identified as a serious virulence factor in staphylococci and increases their antimicrobial resistance. This study aimed to investigate the biofilm forming ability of staphylococci isolated from cow milk samples. Moreover, we assessed the antibiofilm activity of silver nanoparticles (AgNPs) against methicillin resistant (MRSA) and biofilm forming staphylococci. The results revealed that 82.14% (23/28) and 91.66% (11/12) of the coagulase positive staphylococci (CPS) and coagulase negative Staphylococci (CNS) isolates, respectively produced biofilm on Congo red agar (CRA). In the case of the microtiter plates (MTP) method, all CPS and CNS isolates produced biofilm at different levels. These results revealed a substantial agreement between CRA and MTP results according to the kappa coefficient test (kappa value = 0.773). Staphylococcus aureus species specific nuc gene and the determinant of methicillin resistance (mecA) gene were amplified from S. aureus isolates (n=10). The intercellular adhesion gene A (icaA), and intercellular adhesion gene D (icaD) were amplified from all the CPS and CNS isolates, but none of the isolates were positive for the biofilm associated protein (bap) gene. Antibiotic susceptibility testing showed that all isolates were oxacillin resistant. AgNPs (100 μg/mL) inhibited the growth of Staphylococci isolates (inhibition zone diameters ranged from 22 to 28 mm). AgNPs decreased biofilm formation in the biofilm forming Staphylococci isolates with percent ranged from 67.05 to 98.02% using MTP assay. In conclusion, AgNPs have antistaphylococcal activity and inhibit biofilm formation. [ABSTRACT FROM AUTHOR]

Background and Aim: Bovine papillomaviruses (BPV) are a heterogeneous group of oncoviruses, distributed globally, which produce major economic losses. In the current study, we compared the results of different diagnostic approaches and compared the strains identified in this study with previously characterized strains at local and international levels. Materials and Methods: Samples of skin warts were collected from five bovines with generalized papillomatosis from two Egyptian provinces, Menya and Ismailia, in 2020. Electron microscopy, molecular characterization, histopathological, and immunohistochemical examination were performed. Results: BPV was detected using electron microscopy in the collected samples. Using molecular characterization, BPV-2 was successfully identified for 1st time in Egypt. The strain has 99.6% identity with the BPV-2 reference strains obtained from GenBank. These results were supported by histopathology and immunohistochemistry examination. Partial nucleotide sequences of the L1 gene were submitted to GenBank with accession numbers MW289843 and MW289844. Conclusion: BPV-2 was reported for 1st time in the current study. The strain was identified grossly, microscopically, and pathologically and confirmed using molecular approaches. All results were consistent. The sequence analysis revealed that this strain has high sequence similarity to the reference Deltapapillomavirus-4, BPV-2 strains from Brazil and China. [ABSTRACT FROM AUTHOR]

Pseudomonas aeruginosa is known to be multidrug-resistant organisms so its infection is challenging. This study aimed to use the sponge-like reduced protocol in preparation of P. aeruginosa ghosts (PAGs) as a vaccine alternative and evaluate its competency in stimulating the immune response in Nile tilapia. Characterization of PAGs was done using the light, fluorescent and transmission electron microscope. 240 fish have been divided into four groups (60 fish each; three groups were injected with a high, medium, or low dose of PAGs, and a control group. Total and differential leukocyte count, phagocytic activity, lysozyme activity, and gene expression of some immune-related genes were done after the first and booster ghost dose injection. All fish groups were challenged intraperitoneally with P. aeruginosa (1 × 107 CFU ml−1); the mean percent mortality was calculated. Significant immunization potency of the large dose of PAGs was prominent. It is associated with a significant increased number of WBCs, heterophile, lymphocytes, and monocytes. Also the phagocytic activity and indexes were significantly increased by the high and moderate dose of PAGs. Additionally, significant upregulation of immune-related gene (MHC-II) and inflammatory-related gene (IL8) and maintained expression level of TLR7 were recorded. We conclude that chemically prepared P. aeruginosa ghosts maintained both the 3D structure and surface molecules of live bacteria and also are capable of inducing specific immune responses in Nile Tilapia, and reduced mortalities in challenged fish. Our results indicate the advantage of this procedure for production of bacterial ghost, which can be used in wide a range of hosts. [ABSTRACT FROM AUTHOR]

Immunity occupies the top priority in aquaculture. Great efforts have been made to study fish immunity, but little is known about the immunity of grey mullet, Mugil cephalus despite of its importance. We evaluated the effect of different doses (0, 1, 10 and 100 µg/kg body weight) of lipopolysaccharide (LPS) on the expression of non‐specific immune response genes (interleukin (il) 1β, il8, il10 and tumour necrosis factor alpha (tnfα)) in the liver, as well as its effect on the fractionation of serum protein in juvenile grey mullet along different times and concentrations. Analysis revealed that LPS initially caused an upregulation in the studied cytokines. After that, transcripts levels were switched sequentially between downregulation and upregulation, ending with an upregulation at 1 week post injection in il8, il10 and tnfα. Regarding il1β, its initial upregulation was followed by gradual decreases, which reached a marked downregulation at 1 week post injection. Protein fractionation exhibited many changes among doses and time. Nine fractions were discernable in protein electrophoresis of serum in all doses. The most pronounced changes were detected in fractions 7–9 (generally refer to γ globulins or immunoglobulins) using densitometric analysis. In addition, LPS suggested to modulate the levels of serum transferrin. It is known that LPS is a component of the cell wall of Gram negative bacteria, and this study sheds light on the molecular fitness mechanisms against bacterial infection, which could help in developing a strategy to improve resistance to bacterial diseases, or possibly to enhance immune response in grey mullet. [ABSTRACT FROM AUTHOR]

Few data are available on the thermal tolerance of Nile tilapia fish larvae in relation to their immune status and survival. The aims of this work were to evaluate the immune status of one day old Nile tilapia (Oreochromis niloticus) larval stage collected at the beginning (March), middle (August) and at the end (October) of hatching season through morphometric assessment of the larvae parameters including yolk sac diameter, body length and width as well as the expression of some immune-related genes (rag, sacs and tlr), inflammatory (il1b and il8) and stress related genes (hsp27 , hsp70). Also, to compare the effect of three different immunostimulants (β-glucan, Vitamin C, and methionine/lysine amino acids mix) on the expression of the studied genes at two variant temperatures (23 ± 1 °C and 30 ± 1 °C) in experimental study for 21 days. The immune status of Nile tilapia is affected by thermal fluctuation throughout the hatching season reflected by altered yolk sac size, length, and expression of the immune and stress related genes of the larvae, the best performances was observed at the beginning of the hatching season (March). High temperature (30 °C) suppress immune and stress responses throughout downregulation of all the genes under study, mask any effects for the immunostimulants, increased mortality in fish larvae suggesting narrow thermal tolerance range for the larvae compared with the adult fish. We recommend the use of amino acid mix as immunostimulant for Nile tilapia larvae, it reduces the mortality percentage and improve cellular response. Also, the use of β-glucan should be prohibited during this developmental stage of larvae, it induced the highest mortality percentage. • Nile tilapia larvae hatched in March has larger yolk sac and body length, better expression of immune and stress genes. • High temperature (30 °C) impair gene expression and increased mortality in the larvae. • Nile tilapia larvae has narrower thermal tolerance range than the adult fish. • Amino acid mix is recommended for Nile tilapia larvae, it reduce the mortality % and improve cellular response. • β-glucan should be prohibited during this developmental stage of larvae, it induced the highest mortality %. [ABSTRACT FROM AUTHOR]

LPS significantly changed the lymphocytes count at different doses and times postinjection without interaction between LPS doses and time ( I p i = .002 for LPS; I p i = .015 for time; I p i > .05 for interaction). GLO:7ZE/01jan20:are14309-fig-0003.jpg PHOTO (COLOR): The effects of different doses of LPS and time intervals on the catalase (CAT) enzyme activities (U/g tissue) in the liver of grey mullet, Mugil cephalus. Catalase enzyme, H/L ratio, lipopolysaccharides, Mugil cephalus, oxidative stress, sodium oxide dismutase. [Extracted from the article]

• Characterization of AIV-H9N2, pathogenicity and seroprevalence in poultry flocks were conducted. • Interestingly, the PI of the H9N2 broiler strain ranged 1.2–1.9, indicating a high pathogenicity. • A firstly recorded clinical signs, lesions and IHC revealed a systemic infection of H9N2. • A higher seroprevalence was shown in backyard chicken flocks (57.7%) than duck flocks (12.2%). • As a first report, a tested high pathogenicity H9N2 virus requires a continuous monitoring. This study was conducted to perform the comparative molecular characterization of avian influenza virus (AIV) H9N2, pathogenicity and seroprevalence in commercial and backyard poultry flocks. Fifty commercial poultry flocks were investigated between 2012 and 2015. Eighteen flocks (36%) out of 50 were positive HA. Seven (38.9%) out of 18 were positive by chromatographic strip test for AI common antigen. By Real-time RT-PCR, only two flocks were positive H9. The molecular characterization of two different AI-H9N2 viruses, one isolated from a broiler flock (A/chicken/Egypt/Mansoura-18/2013) and the other from a layer flock (A/chicken/Egypt/Mansoura-36/2015) was conducted on HA gene. Moreover, a higher seroprevalence, using the broiler strain as a known antigen, was shown in backyard chicken flocks 15/26 (57.7%) than duck flocks 9/74 (12.2%). Interestingly, the pathogenicity index (PI) of the H9N2 broiler strain in inoculated experimental chickens ranged from 1.2 (oculonasal route) to 1.9 (Intravenous route). The PI indicated a highly pathogenic effect, with high mortality (up to 100%) in the inoculated chickens correlated with the high mortality (80%) in the flock where the virus was isolated. The firstly recorded clinical signs, including cyanosis in the combs and wattles and subcutaneous haemorrhages in the leg shanks and lesions, as well as histopathology and immunohistochemistry, revealed a systemic infection of the high pathogenicity with the H9N2 virus. Conversely, the H9N2 layer strain showed a low pathogenicity. In conclusion, as a first report, the molecular analysis and pathogenicity of the tested strains confirmed the presence of a high pathogenicity AIV-H9N2 with systemic infections. [ABSTRACT FROM AUTHOR]

Efficacy maximization of inactivated avian influenza vaccine using safe adjuvants was investigated. Chitosan nanoparticles were prepared by ionic gelation method with average size of 150 nm and their Zeta potential was 11.5 mV. After encapsulation of avian influenza vaccine, the average size was 397 nm and Zeta potential was 4.29 mV. The highest HI antibody titer results were shown in chicken group vaccinated with inactivated avian influenza virus AIV-chitosan followed by the group vaccinated with inactivated AIV-chitosan nanoparticles then the group vaccinated with oil inactivated AIV vaccine, on using chicken antigen at 2 weeks post second vaccination. Upon using duck antigen, the highest HI antibody titers were shown in chicken group vaccinated with inactivated AIV oil emulsion vaccine followed by chicken group vaccinated with AIV-chitosan nanoparticles then the group vaccinated with AIV–chitosan. Chicken in the group vaccinated with AIV-chitosan nanoparticles induced the best results of lymphocyte proliferation assay. The results of phagocytic activity percentage and phagocytic index of AIV-chitosan nanoparticles and AIV–chitosan groups at 3 days post first vaccination were increased significantly in comparison with other groups, whereas at 14 days post first vaccination, group vaccinated with AIV-chitosan nanoparticles showed significant increase in phagocytic activity percentage and phagocytic index. [ABSTRACT FROM AUTHOR]

In many enterprises and the private sector, the Internet of Things (IoT) has spread globally. The growing number of different devices connected to the IoT and their various protocols have contributed to the increasing number of attacks, such as denial-of-service (DoS) and remote-to-local (R2L) ones. There are several approaches and techniques that can be used to construct attack detection models, such as machine learning, data mining, and statistical analysis. Nowadays, this technique is commonly used because it can provide precise analysis and results. Therefore, we decided to study the previous literature on the detection of IoT attacks and machine learning in order to understand the process of creating detection models. We also evaluated various datasets used for the models, IoT attack types, independent variables used for the models, evaluation metrics for assessment of models, and monitoring infrastructure using DevSecOps pipelines. We found 49 primary studies, and the detection models were developed using seven different types of machine learning techniques. Most primary studies used IoT device testbed datasets, and others used public datasets such as NSL-KDD and UNSW-NB15. When it comes to measuring the efficiency of models, both numerical and graphical measures are commonly used. Most IoT attacks occur at the network layer according to the literature. If the detection models applied DevSecOps pipelines in development processes for IoT devices, they were more secure. From the results of this paper, we found that machine learning techniques can detect IoT attacks, but there are a few issues in the design of detection models. We also recommend the continued use of hybrid frameworks for the improved detection of IoT attacks, advanced monitoring infrastructure configurations using methods based on software pipelines, and the use of machine learning techniques for advanced supervision and monitoring. [ABSTRACT FROM AUTHOR]

Exposure to ionizing radiation usually results in cellular oxidative damage and may induce liver toxicity. The efficiency of the ethanol extracts of Washingtonia filifera (EWF) and Washingtonia robusta (EWR) leaves in alleviating γ-radiation-induced oxidative hepatotoxicity was herein explored. Proximate and macronutrient composition of the leaves was determined to establish reliable quality control criteria. Colorimetric estimation of total phenolic (TPC) and flavonoid (TFC) contents revealed their occurrence in larger amounts in EWR. In vitro evaluation of the antioxidant capacity by 2,2-azinobis (3-ethylbenzothiazoline-6-sulfonic acid (ABTS) and ferric reducing antioxidant power (FRAP) assays confirmed higher efficiency of EWR designating a close correlation with phenolic composition. Four phenolics, viz., naringenin, kaempferol, quercetin, and gallic acid, were isolated from EWR. In vivo assessment of the extracts' antioxidant potential was performed on γ-irradiated (7.5 Gy) female rats. EWR was found more efficient in restoring the elevated liver index, ALT, albumin, cholesterol, and reactive oxygen species (ROS) levels. Both extracts ameliorated the increase in the stimulator of interferon gene (STING) expression. Bioactivity was confirmed by immuno-histochemical examination of inflammatory and apoptotic biomarkers (TNF-α, IL-6 and caspase-3) and histopathological architecture. In addition, the interactions of the isolated compounds with STING were assessed in silico by molecular docking. Therefore, Washingtonia robusta leaves might be suggested as a valuable nutritional supplement to alleviate radiotherapy-induced hepatotoxicity. [ABSTRACT FROM AUTHOR]

Highly pathogenic avian influenza (HPAI) H5N1 and H5N8 have become endemic among domestic poultry in Egypt since 2006 and 2016, respectively. In parallel, the low pathogenic avian influenza H9N2 virus has been endemic since 2010. Despite the continuous circulation of these subtypes for several years, no natural reassortant has been detected so far among the domestic poultry population in Egypt. In this study, the HPAI (H5N2) virus was isolated from a commercial duck farm, giving evidence of the emergence of the first natural reassortment event in domestic poultry in Egypt. The virus was derived as a result of genetic reassortment between avian influenza viruses of H5N8 and H9N2 subtypes circulating in Egypt. The exchange of the neuraminidase segment and high number of acquired mutations might be associated with an alteration in the biological propensities of this virus. [ABSTRACT FROM AUTHOR]