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Intraepithelial lymphocytes (IELs) provide the first line of immunological defense after the invasion of the intestine by a pathogen. To understand the changes of IEL response in chickens, we measured the population of different subsets of avian IELs at different time points after primary inoculation of Newcastle disease virus (NDV) lentogenic strain (LaSota) and subsequent challenge with NDV velogenic strain- genotypes VII and VIII. Furthermore, NDV shed after each treatment was quantified. Specific-pathogen-free chickens were randomly divided into six groups of chickens, one to six, inoculated with phosphate buffered saline; NDV lentogenic strain (LaSota); genotype VII (GVII); LaSota and challenged with GVII (LSGVII); genotype VIII (GVIII); and group of LaSota and challenged with GVIII (LSGVIII). The chickens were euthanized at 12, 36, and 60 h postchallenge. Immunophenotyping of CD25

In spite of the available information on the role of natural killer (NK) cells in several viral infections, the interactions between chicken intraepithelial-NK (IEL-NK) cells and Newcastle disease virus (NDV) are poorly understood. In this study, we investigated these interactions following the inoculation of chickens with NDV vaccine strain LaSota and subsequent challenge with velogenic NDV (vNDV) genotype VII (GVII) and VIII (GVIII), through quantification of IEL-NK cell's apoptosis and expression profiling of its surface receptors. Specific-pathogen-free chickens were randomly divided into six groups, as follows: one group of an uninfected control, one group infected with NDV LaSota, two groups each infected with either GVII or GVIII, and two groups inoculated with NDV LaSota and challenged with either GVII (LaSota-genotype VII [LSGVII]) or GVIII (LaSota-genotype VIII [LSGVIII]). Avian intraepithelial lymphocytes (IEL) were isolated from the duodenal loops, and CD3- cells were characterized. Immunophenotyping and apoptosis analysis of CD3-/CD25+/CD45+IEL NK cells were conducted using a flow cytometer. In addition, a gene expression study was conducted using real-time quantitative PCR. Data were analyzed using two-way analysis of variance. The results showed that vNDV GVII or GVIII caused apoptosis of IEL-NK cells; however, following inoculation of LSGVII or LSGVIII, the effect of vNDV GVII and GVIII to cause a reduction in the population of viable IEL-NK cells was significantly reduced. Furthermore, the expression profiles of activating receptors CD69, NK-lysin, and IFN-γ, were generally upregulated in chickens inoculated with LSGVII or LSGVIII. In contrast, B-NK, an inhibitory receptor, was downregulated in these treatment groups. In NDV GVII- and GVIII-challenged groups, however, B-NK was upregulated, whereas the other receptors were generally downregulated. The findings of this study showed that NDV vaccine strain LaSota may prevent apoptosis and cause upregulation of activating receptors of chicken IEL-NK cells in velogenic virus-challenged settings.Perfiles de expresión de genes relacionados con la inmunidad y estudio de apoptosis de células asesinas naturales intraepiteliales aviares en pollos inoculados con la cepa vacunal del virus de la enfermedad de Newcastle (NDV) y desafiados con de Newcastle virulento. A pesar de la información disponible sobre el papel de las células asesinas naturales (NK) en varias infecciones virales, se conoce poco acerca de las interacciones entre las células NK intraepiteliales de pollo (IEL-NK) y el virus de la enfermedad de Newcastle (NDV). En este estudio, investigamos estas interacciones luego de la inoculación de pollos con la cepa vacunal LaSota y con el desafío posterior con los genotipo VII (GVII) y VIII (GVIII) velogénico de NDV (vNDV), mediante la cuantificación de la apoptosis de las células IEL-NK y los perfiles de expresión de sus receptores de superficie. Los pollos libres de patógenos específicos se dividieron aleatoriamente en seis grupos, de la siguiente manera: un grupo de control no infectado, un grupo infectado con LaSota, dos grupos cada uno infectado con GVII o GVIII, y dos grupos inoculados con LaSota y desafiados con ya sea el genotipo GVII (LaSota-genotipo VII [LSGVII]) o con el genotipo GVIII (LaSota-genotipo VIII [LSGVIII]). Se aislaron células NK intraepiteliales de pollo de las asas duodenales y se caracterizaron las células CD3-. La inmunofenotipificación y el análisis de apoptosis de las células NK CD3-/CD25+/CD45+IEL se realizaron utilizando citometría de flujo. Además, se realizó un estudio de expresión de genes mediante PCR cuantitativa en tiempo real. Los datos se analizaron utilizando un análisis de varianza de dos vías. Los resultados mostraron que el virus de Newcastle genotipos GVII o GVIII causaron apoptosis de células NK intraepiteliales; sin embargo, después de por los tratamientos LaSota-genotipo VII o LaSota-genotipo VIII, el efecto de del virus virulento de Newcastle GVII y GVIII para provocar una reducción en la población de células NK intraepiteliales viables se redujo significativamente. Además, los perfiles de expresión de los receptores activadores CD69, NK-lisina e IFN-γ generalmente aumentaron en pollos inoculados con los tratamientos LaSota-genotipo VII o LaSota-genotipo VIII. Por el contrario, B-NK, que es un receptor inhibidor, se reguló a la baja en estos grupos de tratamiento. Sin embargo, en los grupos expuestos a los virus de Newcastle genotipos GVII y GVIII, el gene B-NK estaba regulado al alza, mientras que los otros receptores generalmente estaban regulados a la baja. Los hallazgos de este estudio mostraron que la cepa vacunal LaSota puede prevenir la apoptosis y causar una regulación al alza de los receptores activadores de las células NK intraepiteliales de pollo en entornos expuestos al virus velogénico.

This cross sectional survey was conducted from July to December 2015 in order to investigate the burden of gastrointestinal helminthes among guinea fowls in Gombe, Northeastern Nigeria. A total of six hundred fowls (viscera) were purchased from six randomly selected slaughter slabs. Out of the 600 birds examined, 479 (79.83%; 95% CI: 76.4, 82.9) were found harbouring one or more gastrointestinal helminthes. Of this, 238 birds (39.7%; 35.8, 43.6) were infected by nematode species and 392 birds (65.3%; 61.4, 69.0) by cestode species. A total of nine nematodes and seven cestodes species were recovered from these birds. There was no any trematode observed among the studied birds. The prevalences of the nematodes identified in descending order were: Ascaridia galli 56.7% (52.7, 60.6); Ascaridia numidae 38.0% (34.2, 42.0); Heterakis gallinarum 17.2% (14.4, 20.4); Heterakis meleagridis 8.3% (6.4, 10.8); Strongyloides avium 3.5% (2.3, 5.3); Subulura brumpti 3.2% (2.0, 5.0); Gongylonema ingluvicola 2.2% (1.3, 3.7) and both Dispharynx spiralis and Tetrameres numidae had 0.7% (0.3, 1.7). While for cestodes: Raillietina tetragona 72.8% (69.1, 76.2); Raillietina echinobothrida 67.3% (63.5, 71.0); Raillietina cesticillus 50% (46.0, 54.0); Raillietina magninumida 25.7% (22.3, 29.3); Hymenolopsis cantaniana 17.3% (14.5, 20.6); Davainea nana 4.2% (2.8, 6.1) and the lowest was observed in Choanotaenia infundibulum with 2% (1.2, 3.5). Infection rates did not differ significantly based on sex (P > 0.05). However, the occurrence of mixed infection as compared with single infection was statistically significant in both cestodes and nematodes (P

Objective: This study was designed to investigate the seroprevalence of Chicken Infectious Anemia Virus (CIAV) among selected poultry species in Maiduguri, Nigeria. Materials and method: ELISA kit (X-Ovo FlockscreenTM, Cat. No.V085 5 plates. February, 2014 - Xnew kit format), Chicken serum, enzyme conjugate reagent, adhesive cover, wash buffer, substrate reagent, stop solution. Serum samples from village chickens, broilers, layers, ducks, turkeys and geese in Maiduguri were tested for CIAV antibodies using Enzyme Linked Immunosorbent Assay (ELISA) as per the manufacturers protocols at the Viral Research Laboratory, Faculty of Veterinary Medicine, University of Maiduguri, Nigeria. The results were presented in simple percentages, bar charts and analyzed using SPSS Version 16 software. Results: Out of 944 sera from different species of poultry tested, an overall seroprevalence of 38.5% (n=363/944) was recorded in this study. The species distribution showed village chickens had 41.4% (n=166/944) prevalence, layers with 23.0% (n=12/52), broilers 46.6% (n=146/313), turkeys 23.6% (n=30/127), ducks 13.7% (n=4/29) and geese 22.7% (n=5/22) prevalence for CIAV antibodies. Conclusion: The result of this study shows that CIAV infection is present among different poultry species in the study area and therefore highlight the need for continuous surveillance so as to control further spread of the virus. [J Adv Vet Anim Res 2017; 4(4.000): 385-389]

Background and Aim: Bovine tuberculosis (bTB) still remains a major zoonotic bacterial disease affecting livestock and humans worldwide. The disease remains a poorly managed tropical disease in most developing countries of the world; where in addition to productivity losses and significance in international trade, it posed a major public health threat to both humans and animals. A retrospective study was designed to investigate the occurrence of bTB lesions at Bauchi municipal abattoir. Materials and Methods: The study utilized abattoir records spanning a period of 10 years (2004-2013). The records indicated that a total of 1,08,638 heads of cattle comprising n = 56,070 males and n = 52,570 females were slaughtered at the municipal abattoir during the study period. Results: Of these heads, n = 1230 (1.13%) (95% confidence interval [CI]: 1.07, 1.19) had tuberculous lesions. The annual occurrence during the study period varied significantly (p