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Antigenic and genomic characterization of local fowlpox virus isolate in 2017 [electronic resource]

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Language: English Summary language: Arabic Description: p. 31–39Uniform titles:

Journal of applied veterinary sciences, 2020 v.5 (3)

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Journal of Applied Veterinary Sciences 2020.v.5(3)Summary: This study presents a local isolate of fowl pox virus (FPV) isolated and propagated from backyard naturally infected laying hens in El-Sharkia Governorate, Egypt, during the period of January to November 2017. Isolation and propagation were carried out from collected skin lesions on the chorioallantoic membrane (CAM) and chicken embryo fibroblast (CEF) with obtained 4th passage virus titers 4.0 Log10 EID50/ml at the in CAM and 3.5 Log10 TCID50/ml in CEF respectively. They showed characteristic pock lesions of FPV and cytopathic effect (CPE) of FPV at the 3rd passage on CAM and CEF, respectively. Virus neutralization test (VNT) results confirmed that the obtained isolate is FPV. Molecular characterization of (Sharkia2017/VSVRI) was performed with Polymerase chain reaction (PCR) to amplify 578 bp of P4b (fpv167) gene and 1150 bp of fpv140 gene. Sequence and phylogenetic analysis of both genes confirmed the relatedness of (Sharkia2017/VSVRI) isolate to sub-clade A1 of fowl pox viruses with 99.7-100% identity to fowl pox virus sequences published in GenBank.This study reports the antigenic and genomic characterization of the locally isolated FPV (Sharkia2017/VSVRI) using VNT and PCR confirmed by sequence analysis to help in the production of FPV tissue culture vaccine from the obtained local FPV after confirming its immune response as a candidate vaccine.

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This study presents a local isolate of fowl pox virus (FPV) isolated and propagated from backyard naturally infected laying hens
in El-Sharkia Governorate, Egypt, during the period of January to November 2017. Isolation and propagation were carried out from
collected skin lesions on the chorioallantoic membrane (CAM) and chicken embryo fibroblast (CEF) with obtained 4th passage virus
titers 4.0 Log10 EID50/ml at the in CAM and 3.5 Log10 TCID50/ml in CEF respectively. They showed characteristic pock lesions of
FPV and cytopathic effect (CPE) of FPV at the 3rd passage on CAM and CEF, respectively. Virus neutralization test (VNT) results
confirmed that the obtained isolate is FPV. Molecular characterization of (Sharkia2017/VSVRI) was performed with Polymerase
chain reaction (PCR) to amplify 578 bp of P4b (fpv167) gene and 1150 bp of fpv140 gene. Sequence and phylogenetic analysis
of both genes confirmed the relatedness of (Sharkia2017/VSVRI) isolate to sub-clade A1 of fowl pox viruses with 99.7-100% identity
to fowl pox virus sequences published in GenBank.This study reports the antigenic and genomic characterization of the locally
isolated FPV (Sharkia2017/VSVRI) using VNT and PCR confirmed by sequence analysis to help in the production of FPV tissue culture
vaccine from the obtained local FPV after confirming its immune response as a candidate vaccine.

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