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Introduction of a Newcastle disease virus challenge strain (sub-genotype VII.1.1) isolated in Iran

Newcastle disease virus (NDV) sub-genotype VII.1.1 is the most common circulating NDV in Iran. In this study, a velogenic NDV isolate was plaque purified and then characterized according to Office International des Epizooties (OIE) standard protocols. The biological properties of the purified isolat...

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Autores principales: Khabiri, Aliakbar, Toroghi, Reza, Mohammadabadi, Mohammadreza, Tabatabaeizadeh, Seyed-Elias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Urmia University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10170471/
https://www.ncbi.nlm.nih.gov/pubmed/37181855
http://dx.doi.org/10.30466/vrf.2022.548152.3373
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author Khabiri, Aliakbar
Toroghi, Reza
Mohammadabadi, Mohammadreza
Tabatabaeizadeh, Seyed-Elias
author_facet Khabiri, Aliakbar
Toroghi, Reza
Mohammadabadi, Mohammadreza
Tabatabaeizadeh, Seyed-Elias
author_sort Khabiri, Aliakbar
collection PubMed
description Newcastle disease virus (NDV) sub-genotype VII.1.1 is the most common circulating NDV in Iran. In this study, a velogenic NDV isolate was plaque purified and then characterized according to Office International des Epizooties (OIE) standard protocols. The biological properties of the purified isolate named CH/RT40/IR/2011 were characterized using sequencing and phylogenetic analysis, measurement of pathogenicity indexes and challenge studies. The isolate was plaque purified on chicken embryo fibroblast cells for three rounds and then characterized using molecular and biological approaches. Phylogenetic and evolutionary distance analysis of fusion and hemagglutinin-neuraminidase genes classified the virus in sub-genotype VII.1.1. No mutation was observed in the glycosylation and neutralizing epitope sites of the fusion and hemagglutinin-neuraminidase proteins compared to other reported Iranian NDV VII.1.1 isolates. The presence of the 112RRQKRF117 motif in the fusion protein cleavage site together with mean death time, intracerebral pathogenicity index and intravenous pathogenicity index of 57 hr, 1.80 and 2.50 respectively, revealed that the RT40 isolate was a velogenic NDV. In the challenge study, all chickens were inoculated via eye drop, and intranasal route with RT40 isolate died within a week. While all chickens in the vaccinated and challenged group survived and showed no clinical signs. In conclusion, according to genetic analysis, pathotyping and challenge study, the RT40 isolate was similar to virulent NDVs in Iran and was a suitable candidate for a national standard challenge strain, vaccine trials and vaccine production in commercial levers.
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spelling pubmed-101704712023-05-11 Introduction of a Newcastle disease virus challenge strain (sub-genotype VII.1.1) isolated in Iran Khabiri, Aliakbar Toroghi, Reza Mohammadabadi, Mohammadreza Tabatabaeizadeh, Seyed-Elias Vet Res Forum Original Article Newcastle disease virus (NDV) sub-genotype VII.1.1 is the most common circulating NDV in Iran. In this study, a velogenic NDV isolate was plaque purified and then characterized according to Office International des Epizooties (OIE) standard protocols. The biological properties of the purified isolate named CH/RT40/IR/2011 were characterized using sequencing and phylogenetic analysis, measurement of pathogenicity indexes and challenge studies. The isolate was plaque purified on chicken embryo fibroblast cells for three rounds and then characterized using molecular and biological approaches. Phylogenetic and evolutionary distance analysis of fusion and hemagglutinin-neuraminidase genes classified the virus in sub-genotype VII.1.1. No mutation was observed in the glycosylation and neutralizing epitope sites of the fusion and hemagglutinin-neuraminidase proteins compared to other reported Iranian NDV VII.1.1 isolates. The presence of the 112RRQKRF117 motif in the fusion protein cleavage site together with mean death time, intracerebral pathogenicity index and intravenous pathogenicity index of 57 hr, 1.80 and 2.50 respectively, revealed that the RT40 isolate was a velogenic NDV. In the challenge study, all chickens were inoculated via eye drop, and intranasal route with RT40 isolate died within a week. While all chickens in the vaccinated and challenged group survived and showed no clinical signs. In conclusion, according to genetic analysis, pathotyping and challenge study, the RT40 isolate was similar to virulent NDVs in Iran and was a suitable candidate for a national standard challenge strain, vaccine trials and vaccine production in commercial levers. Urmia University Press 2023 2023-04-15 /pmc/articles/PMC10170471/ /pubmed/37181855 http://dx.doi.org/10.30466/vrf.2022.548152.3373 Text en © 2023 Urmia University. All rights reserved https://creativecommons.org/licenses/by-nc-sa/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.https://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Original Article
Khabiri, Aliakbar
Toroghi, Reza
Mohammadabadi, Mohammadreza
Tabatabaeizadeh, Seyed-Elias
Introduction of a Newcastle disease virus challenge strain (sub-genotype VII.1.1) isolated in Iran
title Introduction of a Newcastle disease virus challenge strain (sub-genotype VII.1.1) isolated in Iran
title_full Introduction of a Newcastle disease virus challenge strain (sub-genotype VII.1.1) isolated in Iran
title_fullStr Introduction of a Newcastle disease virus challenge strain (sub-genotype VII.1.1) isolated in Iran
title_full_unstemmed Introduction of a Newcastle disease virus challenge strain (sub-genotype VII.1.1) isolated in Iran
title_short Introduction of a Newcastle disease virus challenge strain (sub-genotype VII.1.1) isolated in Iran
title_sort introduction of a newcastle disease virus challenge strain (sub-genotype vii.1.1) isolated in iran
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10170471/
https://www.ncbi.nlm.nih.gov/pubmed/37181855
http://dx.doi.org/10.30466/vrf.2022.548152.3373
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