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Pathogenesis and Chronologic Localization of the Human Influenza A (H1N1) Virus in Cotton Rats
OBJECTIVES: We aimed to evaluate the pathogenesis and chronologic localization of human influenza A (H1N1) virus in experimentally infected cotton rats. METHODS: The animals were intranasally inoculated with 10(7) plaque-forming units of A/Solomon Islands/3/2006 (H1N1) influenza virus and evaluated...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766908/ https://www.ncbi.nlm.nih.gov/pubmed/24159445 http://dx.doi.org/10.1016/j.phrp.2011.04.005 |
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author | Kwon, Donghyok Shin, Kyeongcheol Shin, Jin-Young Lee, Joo-Yeon Ha, Yooncheol Lee, Nam-Joo Oh, Hee-Bok Chae, Chanhee Kang, Chun |
author_facet | Kwon, Donghyok Shin, Kyeongcheol Shin, Jin-Young Lee, Joo-Yeon Ha, Yooncheol Lee, Nam-Joo Oh, Hee-Bok Chae, Chanhee Kang, Chun |
author_sort | Kwon, Donghyok |
collection | PubMed |
description | OBJECTIVES: We aimed to evaluate the pathogenesis and chronologic localization of human influenza A (H1N1) virus in experimentally infected cotton rats. METHODS: The animals were intranasally inoculated with 10(7) plaque-forming units of A/Solomon Islands/3/2006 (H1N1) influenza virus and evaluated for pathogenicity for a period of 28 days. Virus replication kinetics and pathological properties were assessed chronologically. Acute antiviral responses were evaluated by mean of real-time polymerase chain reaction. RESULTS: Cotton rats infected with A/Solomon Islands/3/2006 virus lost weight until 6 days post-inoculation (DPI) and showed decreased activity until 3 DPI. At necropsy, focal areas of redness and consolidation of lungs were evident at 1, 2, and 3 DPI. Lung histopathology showed moderate to severe interstitial pneumonia, alveolitis and bronchiolitis. Influenza A specific viral protein was detected in bronchiolar epithelial cells, alveolar septa and pneumocytes. Influenza viruses were recovered from the lungs during the early period of infection and the titer peaked at 1 DPI. Viral proteins were detected from 4 hours to 6 hours DPI. These trends correlate with the up-regulation of mRNA expression of the IFN-α, Mx1, and Mx2 genes that play critical roles in the anti-influenza response at the early stage of infection. CONCLUSION: Our results provide evidence that supports the use of cotton rats for the study of influenza virus pathogenesis and the immune response. |
format | Online Article Text |
id | pubmed-3766908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
record_format | MEDLINE/PubMed |
spelling | pubmed-37669082013-10-24 Pathogenesis and Chronologic Localization of the Human Influenza A (H1N1) Virus in Cotton Rats Kwon, Donghyok Shin, Kyeongcheol Shin, Jin-Young Lee, Joo-Yeon Ha, Yooncheol Lee, Nam-Joo Oh, Hee-Bok Chae, Chanhee Kang, Chun Osong Public Health Res Perspect Original Article OBJECTIVES: We aimed to evaluate the pathogenesis and chronologic localization of human influenza A (H1N1) virus in experimentally infected cotton rats. METHODS: The animals were intranasally inoculated with 10(7) plaque-forming units of A/Solomon Islands/3/2006 (H1N1) influenza virus and evaluated for pathogenicity for a period of 28 days. Virus replication kinetics and pathological properties were assessed chronologically. Acute antiviral responses were evaluated by mean of real-time polymerase chain reaction. RESULTS: Cotton rats infected with A/Solomon Islands/3/2006 virus lost weight until 6 days post-inoculation (DPI) and showed decreased activity until 3 DPI. At necropsy, focal areas of redness and consolidation of lungs were evident at 1, 2, and 3 DPI. Lung histopathology showed moderate to severe interstitial pneumonia, alveolitis and bronchiolitis. Influenza A specific viral protein was detected in bronchiolar epithelial cells, alveolar septa and pneumocytes. Influenza viruses were recovered from the lungs during the early period of infection and the titer peaked at 1 DPI. Viral proteins were detected from 4 hours to 6 hours DPI. These trends correlate with the up-regulation of mRNA expression of the IFN-α, Mx1, and Mx2 genes that play critical roles in the anti-influenza response at the early stage of infection. CONCLUSION: Our results provide evidence that supports the use of cotton rats for the study of influenza virus pathogenesis and the immune response. 2011-04-13 2011-06 /pmc/articles/PMC3766908/ /pubmed/24159445 http://dx.doi.org/10.1016/j.phrp.2011.04.005 Text en © 2011 Published by Elsevier B.V. on behalf of Korea Centers for Disease Control and Prevention. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kwon, Donghyok Shin, Kyeongcheol Shin, Jin-Young Lee, Joo-Yeon Ha, Yooncheol Lee, Nam-Joo Oh, Hee-Bok Chae, Chanhee Kang, Chun Pathogenesis and Chronologic Localization of the Human Influenza A (H1N1) Virus in Cotton Rats |
title | Pathogenesis and Chronologic Localization of the Human Influenza A (H1N1) Virus in Cotton Rats |
title_full | Pathogenesis and Chronologic Localization of the Human Influenza A (H1N1) Virus in Cotton Rats |
title_fullStr | Pathogenesis and Chronologic Localization of the Human Influenza A (H1N1) Virus in Cotton Rats |
title_full_unstemmed | Pathogenesis and Chronologic Localization of the Human Influenza A (H1N1) Virus in Cotton Rats |
title_short | Pathogenesis and Chronologic Localization of the Human Influenza A (H1N1) Virus in Cotton Rats |
title_sort | pathogenesis and chronologic localization of the human influenza a (h1n1) virus in cotton rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766908/ https://www.ncbi.nlm.nih.gov/pubmed/24159445 http://dx.doi.org/10.1016/j.phrp.2011.04.005 |
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