Molecular Analysis of Newcastle Disease Virus Isolated from A Vaccinated Layer Farm in Indonesia

2nd International Conference on Biosciences

Shofa, M.^1 ; Wibawan, I.W.T.^1 ; Zarkasie, K.^2 ; Setiyaningsih, S.^1

Medical Microbiology, Department of Animal Disease and Veterinary Public Health Faculty of Veterinary Medicine, Bogor Agricultural University, Darmaga, Bogor

16680, Indonesia^1

PT. IPB Shigeta Animal Pharmaceuticals, Bogor Agricultural University, Darmaga, Bogor

16680, Indonesia^2

关键词: Amino acid sequence;    Cleavage sites;    Molecular analysis;    Neuraminidase;    Newcastle disease virus;    phylogenetic;    Phylogenetic analysis;    Prevention measures;   

Others  :  https://iopscience.iop.org/article/10.1088/1755-1315/197/1/012044/pdf
DOI  :  10.1088/1755-1315/197/1/012044

来源: IOP

【 摘 要 】

Newcastle disease (ND) was first identified in Bogor, Java, Indonesia in 1926 and became major infectious in global commercial poultry which has morbidity and mortality rate up to 100%. Vaccination is one of prevention measures to control Newcastle disease virus (NDV) infection in layer poultry; however, cases of NDV infection are still reported in well vaccinated farms around the world. Molecular determination was aimed to examine genomic variation that might contribute to better control NDV infection. A Virulent NDV was isolated by egg inoculation of sample originated from a vaccinated layer farm suffering significant irreversible egg drop production. The NDV isolate was detected using rRT-PCR targeting region of matrix (M) and fusion (F) gene. Confirmation of virulence was determined by sequence analysis of partial F and hemagglutinin-neuraminidase (HN) genes. Phylogenetic analysis shows the isolate clustered within sub genotype VIIh with Indonesia NDV isolates. Identification of polybasic motif of 112RRRKR/F117 in the cleavage site of fusion protein confirms its virulence. Analysis of putative amino acid sequence highlighted E347K substitution in HN region, which has been reported to affect the capability of NDV in infecting vaccinated poultry. This finding indicates the urgent need of NDV molecular surveillance in vaccinated farms in larger area.