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Course of seasonal influenza A/Brisbane/59/07 H1N1 infection in the ferret
Every year, influenza viruses infect approximately 5-20% of the population in the United States leading to over 200,000 hospitalizations and 36,000 deaths from flu-related complications. In this study, we characterized the immune and pathological progression of a seasonal strain of H1N1 influenza vi...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909963/ https://www.ncbi.nlm.nih.gov/pubmed/20618974 http://dx.doi.org/10.1186/1743-422X-7-149 |
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author | McBrayer, Alexis Camp, Jeremy V Tapp, Ron Yamshchikov, Vladimir Grimes, Sheila Noah, Diana L Jonsson, Colleen B Bruder, Carl E |
author_facet | McBrayer, Alexis Camp, Jeremy V Tapp, Ron Yamshchikov, Vladimir Grimes, Sheila Noah, Diana L Jonsson, Colleen B Bruder, Carl E |
author_sort | McBrayer, Alexis |
collection | PubMed |
description | Every year, influenza viruses infect approximately 5-20% of the population in the United States leading to over 200,000 hospitalizations and 36,000 deaths from flu-related complications. In this study, we characterized the immune and pathological progression of a seasonal strain of H1N1 influenza virus, A/Brisbane/59/2007 in a ferret model. The immune response of the animals showed a dose-dependent increase with increased virus challenge, as indicated by the presence of virus specific IgG, IgM, and neutralizing antibodies. Animals infected with higher doses of virus also experienced increasing severity of clinical symptoms and fever at 2 days post-infection (DPI). Interestingly, weight loss was more pronounced in animals infected with lower doses of virus compared to those infected with a higher dose; these results were consistent with viral titers of swabs collected from the nares, but not the throat. Analyzed specimens included nasal and throat swabs from 1, 3, 5, and 7 DPI as well as tissue samples from caudal lung and nasal turbinates. Viral titers of the swab samples in all groups were higher on 1 and 3 DPI and returned to baseline levels by 7 DPI. Analysis of nasal turbinates indicated presence of virus at 3 DPI in all infected groups, whereas virus was only detected in the lungs of animals in the two highest dose groups. Histological analysis of the lungs showed a range of pathology, such as chronic inflammation and bronchial epithelial hypertrophy. The results provided here offer important endpoints for preclinical testing of the efficacy of new antiviral compounds and experimental vaccines. |
format | Text |
id | pubmed-2909963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29099632010-07-27 Course of seasonal influenza A/Brisbane/59/07 H1N1 infection in the ferret McBrayer, Alexis Camp, Jeremy V Tapp, Ron Yamshchikov, Vladimir Grimes, Sheila Noah, Diana L Jonsson, Colleen B Bruder, Carl E Virol J Short Report Every year, influenza viruses infect approximately 5-20% of the population in the United States leading to over 200,000 hospitalizations and 36,000 deaths from flu-related complications. In this study, we characterized the immune and pathological progression of a seasonal strain of H1N1 influenza virus, A/Brisbane/59/2007 in a ferret model. The immune response of the animals showed a dose-dependent increase with increased virus challenge, as indicated by the presence of virus specific IgG, IgM, and neutralizing antibodies. Animals infected with higher doses of virus also experienced increasing severity of clinical symptoms and fever at 2 days post-infection (DPI). Interestingly, weight loss was more pronounced in animals infected with lower doses of virus compared to those infected with a higher dose; these results were consistent with viral titers of swabs collected from the nares, but not the throat. Analyzed specimens included nasal and throat swabs from 1, 3, 5, and 7 DPI as well as tissue samples from caudal lung and nasal turbinates. Viral titers of the swab samples in all groups were higher on 1 and 3 DPI and returned to baseline levels by 7 DPI. Analysis of nasal turbinates indicated presence of virus at 3 DPI in all infected groups, whereas virus was only detected in the lungs of animals in the two highest dose groups. Histological analysis of the lungs showed a range of pathology, such as chronic inflammation and bronchial epithelial hypertrophy. The results provided here offer important endpoints for preclinical testing of the efficacy of new antiviral compounds and experimental vaccines. BioMed Central 2010-07-09 /pmc/articles/PMC2909963/ /pubmed/20618974 http://dx.doi.org/10.1186/1743-422X-7-149 Text en Copyright ©2010 McBrayer 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 | Short Report McBrayer, Alexis Camp, Jeremy V Tapp, Ron Yamshchikov, Vladimir Grimes, Sheila Noah, Diana L Jonsson, Colleen B Bruder, Carl E Course of seasonal influenza A/Brisbane/59/07 H1N1 infection in the ferret |
title | Course of seasonal influenza A/Brisbane/59/07 H1N1 infection in the ferret |
title_full | Course of seasonal influenza A/Brisbane/59/07 H1N1 infection in the ferret |
title_fullStr | Course of seasonal influenza A/Brisbane/59/07 H1N1 infection in the ferret |
title_full_unstemmed | Course of seasonal influenza A/Brisbane/59/07 H1N1 infection in the ferret |
title_short | Course of seasonal influenza A/Brisbane/59/07 H1N1 infection in the ferret |
title_sort | course of seasonal influenza a/brisbane/59/07 h1n1 infection in the ferret |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909963/ https://www.ncbi.nlm.nih.gov/pubmed/20618974 http://dx.doi.org/10.1186/1743-422X-7-149 |
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