Open Access
Research (Published online: 15-07-2018)
8. Molecular characterization of full fusion protein (F) of Newcastle disease virus genotype VIId isolated from Egypt during 2012-2016
Karim M. Selim, Abdullah Selim, Abdelsatar Arafa, Hussein A. Hussein and Ahmed A. Elsanousi
Veterinary World, 11(7): 930-938

Karim M. Selim: National Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, P.O. Box 264-Dokki, Giza 12618, Egypt.
Abdullah Selim: National Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, P.O. Box 264-Dokki, Giza 12618, Egypt.
Abdelsatar Arafa: National Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, P.O. Box 264-Dokki, Giza 12618, Egypt.
Hussein A. Hussein: Department of Virology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
Ahmed A. Elsanousi: Department of Virology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.

doi: 10.14202/vetworld.2018.930-938

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Article history: Received: 27-03-2018, Accepted: 29-05-2018, Published online: 15-07-2018

Corresponding author: Karim M. Selim

E-mail: dr.kareemseleem_87@yahoo.com

Citation: Selim KM, Selim A, Arafa A, Hussein HA, Elsanousi AA (2018) Molecular characterization of full fusion protein (F) of Newcastle disease virus genotype VIId isolated from Egypt during 2012-2016, Veterinary World, 11(7): 930-938.
Abstract

Aim: The aim of this work was to study the full F gene sequence of Newcastle disease virus (NDV) in regard to pathotyping and genotyping and to study the evolution of this NDV in Egypt.

Materials and Methods: The present study was conducted using samples from seven suspected NDV flocks of vaccinated chickens during 2012-2016 from six governorates in Egypt. The NDV was successfully isolated from pathological specimens through inoculation in specific pathogen-free embryonated chicken eggs.

Results: Pathogenicity of the NDV isolates has been estimated through intracerebral pathogenicity index and ranged from 1.66 to 1.73 which indicates the velogenic type of NDV isolates. Pathotyping and genotyping of these isolates were done through sequencing of full-length F gene. Results indicated that the seven NDV isolates showed characteristic cleavage site motif (112RRQKRF117) for the velogenic strains of NDV. Phylogenetic analysis of the F gene clustered these isolates within Group I of genotype VIId within Israeli strains NDV/IS/2015, NDV-Ch/SD883, and most of the Middle East strains. Six of seven sequenced isolates have six potential N-linked glycosylation sites. The neutralization epitope on the five antigenic sites of fusion is conserved in all Egyptian strains of this study except NDV-KFR-B7-2012 which has a substitution at D 170 N in epitope A4. In all our strains, 10 cysteine residues are recorded, except one loss of cysteine at residue 370 in both NDV-EG-35-2014 and NDV-GHB-328F-2016.

Conclusion: All viruses in this study have 52 amino acid substitutions within fusion gene in compared with Lasota strain that reveals importance for its antigenic and structural function. The present work highlights the important need to sequence F gene of NDV genotype VIId to investigate the evolution of this NDV in Egypt.

Keywords: cleavage site, fusion gene, heptad repeat domains.

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