Serological Status for Newcastle Disease Virus in Unvaccinated Indigenous Chickens in Yewa Division of Ogun State, Nigeria

2006 ◽  
Vol 5 (12) ◽  
pp. 1119-1122 ◽  
Author(s):  
M.A. Oyekunle . ◽  
A.O. Talabi . ◽  
A.O. Okeowo .
2017 ◽  
Vol 5 (34) ◽  
Author(s):  
Celia Abolnik ◽  
Chrisborn Mubamba ◽  
George Dautu ◽  
Bruce Gummow

ABSTRACT The first complete genome sequence of an African-origin Newcastle disease virus belonging to genotype XIII is described here. The virulent strain chicken/Zambia/Chiwoko/2015 was isolated from diseased chickens in 2015.


2019 ◽  
Vol 1 (1) ◽  
pp. 027-034
Author(s):  
Peterside Rinle Kumbish ◽  
King Akpofure Nelson Esievo ◽  
James Saidu Ahmed ◽  
Tobias Pwajok Peter Choji ◽  
Gyang Davou Moses ◽  
...  

2020 ◽  
Vol 45 (3) ◽  
Author(s):  
F. O. Olufemi ◽  
O. Olatunji ◽  
E. O. Omoshaba

Several authors have worked on Newcastle Disease (ND) with respect to the incidence, prevalence and epizootiology of the disease and the antibody status in non-vaccinated birds in Nigeria. However, current information on the antibodies of the Newcastle Disease virus in apparently healthy commercial poultry birds with known vaccination records in Abeokuta Metropolis is scanty. This study was conducted, using Heamagglutination Inhibition assay (HI) technique, to detect Newcastle Disease virus (NDV) antibodies in routinely vaccinated commercial poultry birds in the 3 Local Government Areas (LGAs) of Abeokuta that form the Abeokuta metropolis. Haemagglutinating NDV antibodies were detected in the apparently healthy layers thus indicating a widely circulating NDV in areas. A potency test of the vaccines used on the farms was determined using Heamagglutination test and their values ranged between 2 and 2 . The sero-prevalence of NDVantibodies in the 3 LGAs showed there was no significant difference (p >0.05). Of the 120 sera tested, 82 (68.33%) had detectable NDV antibodies but only 81.67% had HI protective titre of > 2 and 18.33% had low seroconversionwith titre 2 or less.


Viruses ◽  
2021 ◽  
Vol 13 (1) ◽  
pp. 103
Author(s):  
Henry M. Kariithi ◽  
Helena L. Ferreira ◽  
Catharine N. Welch ◽  
Leonard O. Ateya ◽  
Auleria A. Apopo ◽  
...  

Kenyan poultry consists of ~80% free-range indigenous chickens kept in small flocks (~30 birds) on backyard poultry farms (BPFs) and they are traded via live bird markets (LBMs). Newcastle disease virus (NDV) was detected in samples collected from chickens, wild farm birds, and other domestic poultry species during a 2017–2018 survey conducted at 66 BPFs and 21 LBMs in nine Kenyan counties. NDV nucleic acids were detected by rRT-PCR L-test in 39.5% (641/1621) of 1621 analyzed samples, of which 9.67% (62/641) were NDV-positive by both the L-test and a fusion-test designed to identify the virulent virus, with a majority being at LBMs (64.5%; 40/62) compared to BPFs (25.5%; 22/62). Virus isolation and next-generation sequencing (NGS) on a subset of samples resulted in 32 complete NDV genome sequences with 95.8–100% nucleotide identities amongst themselves and 95.7-98.2% identity with other east African isolates from 2010-2016. These isolates were classified as a new sub-genotype, V.3, and shared 86.5–88.9% and 88.5–91.8% nucleotide identities with subgenotypes V.1 and V.2 viruses, respectively. The putative fusion protein cleavage site (113R-Q-K-R↓F 117) in all 32 isolates, and a 1.86 ICPI score of an isolate from a BPF chicken that had clinical signs consistent with Newcastle disease, confirmed the high virulence of the NDVs. Compared to genotypes V and VI viruses, the attachment (HN) protein of 18 of the 32 vNDVs had amino acid substitutions in the antigenic sites. A time-scaled phylogeographic analysis suggests a west-to-east dispersal of the NDVs via the live chicken trade, but the virus origins remain unconfirmed due to scarcity of continuous and systematic surveillance data. This study reveals the widespread prevalence of vNDVs in Kenyan backyard poultry, the central role of LBMs in the dispersal and possibly generation of new virus variants, and the need for robust molecular epidemiological surveillance in poultry and non-poultry avian species.


2016 ◽  
Vol 21 (1) ◽  
pp. 235-248
Author(s):  
Amani Saleh ◽  
Rola Ali ◽  
Mohamed Fawzy ◽  
Mokhtar Eltarabily

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