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Experimental infection of hamsters with avian paramyxovirus serotypes 1 to 9
Avian paramyxoviruses (APMVs) are frequently isolated from domestic and wild birds throughout the world and are separated into nine serotypes (APMV-1 to -9). Only in the case of APMV-1, the infection of non-avian species has been investigated. The APMVs presently are being considered as human vaccin...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052182/ https://www.ncbi.nlm.nih.gov/pubmed/21345199 http://dx.doi.org/10.1186/1297-9716-42-38 |
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author | Samuel, Arthur S Subbiah, Madhuri Shive, Heather Collins, Peter L Samal, Siba K |
author_facet | Samuel, Arthur S Subbiah, Madhuri Shive, Heather Collins, Peter L Samal, Siba K |
author_sort | Samuel, Arthur S |
collection | PubMed |
description | Avian paramyxoviruses (APMVs) are frequently isolated from domestic and wild birds throughout the world and are separated into nine serotypes (APMV-1 to -9). Only in the case of APMV-1, the infection of non-avian species has been investigated. The APMVs presently are being considered as human vaccine vectors. In this study, we evaluated the replication and pathogenicity of all nine APMV serotypes in hamsters. The hamsters were inoculated intranasally with each virus and monitored for clinical disease, pathology, histopathology, virus replication, and seroconversion. On the basis of one or more of these criteria, each of the APMV serotypes was found to replicate in hamsters. The APMVs produced mild or inapparent clinical signs in hamsters except for APMV-9, which produced moderate disease. Gross lesions were observed over the pulmonary surface of hamsters infected with APMV-2 & -3, which showed petechial and ecchymotic hemorrhages, respectively. Replication of all of the APMVs except APMV-5 was confirmed in the nasal turbinates and lungs, indicating a tropism for the respiratory tract. Histologically, the infection resulted in lung lesions consistent with bronchointerstitial pneumonia of varying severity and nasal turbinates with blunting or loss of cilia of the epithelium lining the nasal septa. The majority of APMV-infected hamsters exhibited transient histological lesions that self resolved by 14 days post infection (dpi). All of the hamsters infected with the APMVs produced serotype-specific HI or neutralizing antibodies, confirming virus replication. Taken together, these results demonstrate that all nine known APMV serotypes are capable of replicating in hamsters with minimal disease and pathology. |
format | Text |
id | pubmed-3052182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30521822011-03-10 Experimental infection of hamsters with avian paramyxovirus serotypes 1 to 9 Samuel, Arthur S Subbiah, Madhuri Shive, Heather Collins, Peter L Samal, Siba K Vet Res Research Avian paramyxoviruses (APMVs) are frequently isolated from domestic and wild birds throughout the world and are separated into nine serotypes (APMV-1 to -9). Only in the case of APMV-1, the infection of non-avian species has been investigated. The APMVs presently are being considered as human vaccine vectors. In this study, we evaluated the replication and pathogenicity of all nine APMV serotypes in hamsters. The hamsters were inoculated intranasally with each virus and monitored for clinical disease, pathology, histopathology, virus replication, and seroconversion. On the basis of one or more of these criteria, each of the APMV serotypes was found to replicate in hamsters. The APMVs produced mild or inapparent clinical signs in hamsters except for APMV-9, which produced moderate disease. Gross lesions were observed over the pulmonary surface of hamsters infected with APMV-2 & -3, which showed petechial and ecchymotic hemorrhages, respectively. Replication of all of the APMVs except APMV-5 was confirmed in the nasal turbinates and lungs, indicating a tropism for the respiratory tract. Histologically, the infection resulted in lung lesions consistent with bronchointerstitial pneumonia of varying severity and nasal turbinates with blunting or loss of cilia of the epithelium lining the nasal septa. The majority of APMV-infected hamsters exhibited transient histological lesions that self resolved by 14 days post infection (dpi). All of the hamsters infected with the APMVs produced serotype-specific HI or neutralizing antibodies, confirming virus replication. Taken together, these results demonstrate that all nine known APMV serotypes are capable of replicating in hamsters with minimal disease and pathology. BioMed Central 2011 2011-02-23 /pmc/articles/PMC3052182/ /pubmed/21345199 http://dx.doi.org/10.1186/1297-9716-42-38 Text en Copyright ©2011 Samuel et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Samuel, Arthur S Subbiah, Madhuri Shive, Heather Collins, Peter L Samal, Siba K Experimental infection of hamsters with avian paramyxovirus serotypes 1 to 9 |
title | Experimental infection of hamsters with avian paramyxovirus serotypes 1 to 9 |
title_full | Experimental infection of hamsters with avian paramyxovirus serotypes 1 to 9 |
title_fullStr | Experimental infection of hamsters with avian paramyxovirus serotypes 1 to 9 |
title_full_unstemmed | Experimental infection of hamsters with avian paramyxovirus serotypes 1 to 9 |
title_short | Experimental infection of hamsters with avian paramyxovirus serotypes 1 to 9 |
title_sort | experimental infection of hamsters with avian paramyxovirus serotypes 1 to 9 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052182/ https://www.ncbi.nlm.nih.gov/pubmed/21345199 http://dx.doi.org/10.1186/1297-9716-42-38 |
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