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Experimental avian paramyxovirus serotype-3 infection in chickens and turkeys
Avian paramyxoviruses (APMV) are divided into nine serotypes. Newcastle disease virus (APMV-1) is the most extensively characterized, while relatively little information is available for the other APMV serotypes. In the present study, we examined the pathogenicity of two divergent strains of APMV-3,...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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EDP Sciences
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2939697/ https://www.ncbi.nlm.nih.gov/pubmed/20663473 http://dx.doi.org/10.1051/vetres/2010042 |
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author | Kumar, Sachin Militino Dias, Flavia Nayak, Baibaswata Collins, Peter L. Samal, Siba K. |
author_facet | Kumar, Sachin Militino Dias, Flavia Nayak, Baibaswata Collins, Peter L. Samal, Siba K. |
author_sort | Kumar, Sachin |
collection | PubMed |
description | Avian paramyxoviruses (APMV) are divided into nine serotypes. Newcastle disease virus (APMV-1) is the most extensively characterized, while relatively little information is available for the other APMV serotypes. In the present study, we examined the pathogenicity of two divergent strains of APMV-3, Netherlands and Wisconsin, in (i) 9-day-old embryonated chicken eggs, (ii) 1-day-old specific pathogen free (SPF) chicks and turkeys, and (iii) 2-week-old SPF chickens and turkeys. The mean death time in 9-day-old embryonated chicken eggs was 112 h for APMV-3 strain Netherlands and > 168 h for strain Wisconsin. The intracerebral pathogenicity index in 1-day-old chicks for strain Netherlands was 0.39 and for strain Wisconsin was zero. Thus, both strains are lentogenic. Both the strains replicated well in brain tissue when inoculated intracerebrally in 1-day-old SPF chicks, but without causing death. Mild respiratory disease signs were observed in 1-day-old chickens and turkeys when inoculated through oculonasal route with either strain. There were no overt signs of illness in 2-weeks-old chickens and turkeys by either strain, although all the birds seroconverted after infection. The viruses were isolated predominantly from brain, lungs, spleens, trachea, pancreas and kidney. Immunohistochemistry studies also showed the presence of large amount of viral antigens in both epithelial and sub-epithelial lining of respiratory and alimentary tracts. Our result suggests systemic spread of APMV-3 even though the viral fusion glycoprotein does not contain the canonical furin proteases cleavage site. Furthermore, there was little or no disease despite systemic viral spread and abundant viral replication in all the tissues tested. |
format | Text |
id | pubmed-2939697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | EDP Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-29396972010-09-20 Experimental avian paramyxovirus serotype-3 infection in chickens and turkeys Kumar, Sachin Militino Dias, Flavia Nayak, Baibaswata Collins, Peter L. Samal, Siba K. Vet Res Original Article Avian paramyxoviruses (APMV) are divided into nine serotypes. Newcastle disease virus (APMV-1) is the most extensively characterized, while relatively little information is available for the other APMV serotypes. In the present study, we examined the pathogenicity of two divergent strains of APMV-3, Netherlands and Wisconsin, in (i) 9-day-old embryonated chicken eggs, (ii) 1-day-old specific pathogen free (SPF) chicks and turkeys, and (iii) 2-week-old SPF chickens and turkeys. The mean death time in 9-day-old embryonated chicken eggs was 112 h for APMV-3 strain Netherlands and > 168 h for strain Wisconsin. The intracerebral pathogenicity index in 1-day-old chicks for strain Netherlands was 0.39 and for strain Wisconsin was zero. Thus, both strains are lentogenic. Both the strains replicated well in brain tissue when inoculated intracerebrally in 1-day-old SPF chicks, but without causing death. Mild respiratory disease signs were observed in 1-day-old chickens and turkeys when inoculated through oculonasal route with either strain. There were no overt signs of illness in 2-weeks-old chickens and turkeys by either strain, although all the birds seroconverted after infection. The viruses were isolated predominantly from brain, lungs, spleens, trachea, pancreas and kidney. Immunohistochemistry studies also showed the presence of large amount of viral antigens in both epithelial and sub-epithelial lining of respiratory and alimentary tracts. Our result suggests systemic spread of APMV-3 even though the viral fusion glycoprotein does not contain the canonical furin proteases cleavage site. Furthermore, there was little or no disease despite systemic viral spread and abundant viral replication in all the tissues tested. EDP Sciences 2010-07-23 2010 /pmc/articles/PMC2939697/ /pubmed/20663473 http://dx.doi.org/10.1051/vetres/2010042 Text en © The authors published by INRA/EDP Sciences, 2010 This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted use, distribution, and reproduction in any noncommercial medium, provided the original work is properly cited. |
spellingShingle | Original Article Kumar, Sachin Militino Dias, Flavia Nayak, Baibaswata Collins, Peter L. Samal, Siba K. Experimental avian paramyxovirus serotype-3 infection in chickens and turkeys |
title | Experimental avian paramyxovirus serotype-3 infection in chickens and turkeys |
title_full | Experimental avian paramyxovirus serotype-3 infection in chickens and turkeys |
title_fullStr | Experimental avian paramyxovirus serotype-3 infection in chickens and turkeys |
title_full_unstemmed | Experimental avian paramyxovirus serotype-3 infection in chickens and turkeys |
title_short | Experimental avian paramyxovirus serotype-3 infection in chickens and turkeys |
title_sort | experimental avian paramyxovirus serotype-3 infection in chickens and turkeys |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2939697/ https://www.ncbi.nlm.nih.gov/pubmed/20663473 http://dx.doi.org/10.1051/vetres/2010042 |
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