Isolation, pathotyping and genotyping of Newcastle disease virus from broiler chickens in Egypt
Journal of Virological Sciences • 2017
Publication Information
Authors
13. Ayman S. El-Habbaa; Gabr F. El-Bagoury; Samar F. El-Adaway; Susan S. El-Mahdy
Keywords
HI; ICPI; Lentogenic; MDT; NDV; PCR; Phylogeny; Velogenic
Journal
Journal of Virological Sciences
Publisher
Scope Med.
Volume
1
Issue
1
Pages
114-122
publication.type
International
Paper Link
Not Available
Supplementary Materials
Not Available
Abstract
Background: In Egypt, outbreaks of Newcastle disease (ND) have been occurring in vaccinated chickens with great economic losses.
Objective: This work aimed for diagnosis and characterization of Newcastle Disease Virus (NDV) from infected broiler chickens in Egypt.
Methods: Suspected virus isolates on embryonated chicken eggs was detected by Hemagglutination (HA) test and identified using hemagglutination inhibition (HI) test. F protein encoding gene of NDV was amplified using Reverse Transcription-Polymerase Chain Reaction (RT-PCR) then subjected for nucleotide and amino acid sequence detection.
Results: NDV Giza 2014 isolate and NDV Qualubiya 2014 were characterized as velogenic and lentogenic strains, respectively using Mean Death Time (MDT), Intracerebral Pathogenicity Index (ICPI) and studying amino acid motif of the F protein cleavage site. Phylogeny put NDV Giza 2014 in a separate branch independent from other Egyptian isolates, however it is more related to Lasota (genotype II) and Clone 30 vaccinal strains, while NDV Qualubiya 2014 was grouped more related to Ulster strain (genotype I) and Australian isolates originating from the same ancestral node however it is distantly related to other Egyptian strains 2005 and 2006 grouped together with a common ancestral node but on a separate branch. These results proved diversity between the isolated velogenic NDV Giza 2014 strain and other vaccinal and circulating NDV strains.
Conclusion: It is concluded that further studies on the antigenic characters of that variant isolate is required to study antigenic variation between NDV strains circulating in Egypt.
Objective: This work aimed for diagnosis and characterization of Newcastle Disease Virus (NDV) from infected broiler chickens in Egypt.
Methods: Suspected virus isolates on embryonated chicken eggs was detected by Hemagglutination (HA) test and identified using hemagglutination inhibition (HI) test. F protein encoding gene of NDV was amplified using Reverse Transcription-Polymerase Chain Reaction (RT-PCR) then subjected for nucleotide and amino acid sequence detection.
Results: NDV Giza 2014 isolate and NDV Qualubiya 2014 were characterized as velogenic and lentogenic strains, respectively using Mean Death Time (MDT), Intracerebral Pathogenicity Index (ICPI) and studying amino acid motif of the F protein cleavage site. Phylogeny put NDV Giza 2014 in a separate branch independent from other Egyptian isolates, however it is more related to Lasota (genotype II) and Clone 30 vaccinal strains, while NDV Qualubiya 2014 was grouped more related to Ulster strain (genotype I) and Australian isolates originating from the same ancestral node however it is distantly related to other Egyptian strains 2005 and 2006 grouped together with a common ancestral node but on a separate branch. These results proved diversity between the isolated velogenic NDV Giza 2014 strain and other vaccinal and circulating NDV strains.
Conclusion: It is concluded that further studies on the antigenic characters of that variant isolate is required to study antigenic variation between NDV strains circulating in Egypt.
Staff Members - Benha University