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A Systematic Molecular Pathology Study of a Laboratory Confirmed H5N1 Human Case

Autopsy studies have shown that human highly pathogenic avian influenza virus (H5N1) can infect multiple human organs other than just the lungs, and that possible causes of organ damage are either viral replication and/or dysregulation of cytokines and chemokines. Uncertainty still exists, partly be...

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Autores principales: Gao, Rongbao, Dong, Libo, Dong, Jie, Wen, Leying, Zhang, Ye, Yu, Hongjie, Feng, Zijian, Chen, Minmei, Tan, Yi, Mo, Zhaojun, Liu, Haiyan, Fan, Yunyan, Li, Kunxiong, Li, Chris Ka-Fai, Li, Dexin, Yang, Weizhong, Shu, Yuelong
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953511/
https://www.ncbi.nlm.nih.gov/pubmed/20976271
http://dx.doi.org/10.1371/journal.pone.0013315
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author Gao, Rongbao
Dong, Libo
Dong, Jie
Wen, Leying
Zhang, Ye
Yu, Hongjie
Feng, Zijian
Chen, Minmei
Tan, Yi
Mo, Zhaojun
Liu, Haiyan
Fan, Yunyan
Li, Kunxiong
Li, Chris Ka-Fai
Li, Dexin
Yang, Weizhong
Shu, Yuelong
author_facet Gao, Rongbao
Dong, Libo
Dong, Jie
Wen, Leying
Zhang, Ye
Yu, Hongjie
Feng, Zijian
Chen, Minmei
Tan, Yi
Mo, Zhaojun
Liu, Haiyan
Fan, Yunyan
Li, Kunxiong
Li, Chris Ka-Fai
Li, Dexin
Yang, Weizhong
Shu, Yuelong
author_sort Gao, Rongbao
collection PubMed
description Autopsy studies have shown that human highly pathogenic avian influenza virus (H5N1) can infect multiple human organs other than just the lungs, and that possible causes of organ damage are either viral replication and/or dysregulation of cytokines and chemokines. Uncertainty still exists, partly because of the limited number of cases analysed. In this study, a full autopsy including 5 organ systems was conducted on a confirmed H5N1 human fatal case (male, 42 years old) within 18 hours of death. In addition to the respiratory system (lungs, bronchus and trachea), virus was isolated from cerebral cortex, cerebral medullary substance, cerebellum, brain stem, hippocampus ileum, colon, rectum, ureter, aortopulmonary vessel and lymph-node. Real time RT-PCR evidence showed that matrix and hemagglutinin genes were positive in liver and spleen in addition to positive tissues with virus isolation. Immunohistochemistry and in-situ hybridization stains showed accordant evidence of viral infection with real time RT-PCR except bronchus. Quantitative RT-PCR suggested that a high viral load was associated with increased host responses, though the viral load was significantly different in various organs. Cells of the immunologic system could also be a target for virus infection. Overall, the pathogenesis of HPAI H5N1 virus was associated both with virus replication and with immunopathologic lesions. In addition, immune cells cannot be excluded from playing a role in dissemination of the virus in vivo.
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spelling pubmed-29535112010-10-25 A Systematic Molecular Pathology Study of a Laboratory Confirmed H5N1 Human Case Gao, Rongbao Dong, Libo Dong, Jie Wen, Leying Zhang, Ye Yu, Hongjie Feng, Zijian Chen, Minmei Tan, Yi Mo, Zhaojun Liu, Haiyan Fan, Yunyan Li, Kunxiong Li, Chris Ka-Fai Li, Dexin Yang, Weizhong Shu, Yuelong PLoS One Research Article Autopsy studies have shown that human highly pathogenic avian influenza virus (H5N1) can infect multiple human organs other than just the lungs, and that possible causes of organ damage are either viral replication and/or dysregulation of cytokines and chemokines. Uncertainty still exists, partly because of the limited number of cases analysed. In this study, a full autopsy including 5 organ systems was conducted on a confirmed H5N1 human fatal case (male, 42 years old) within 18 hours of death. In addition to the respiratory system (lungs, bronchus and trachea), virus was isolated from cerebral cortex, cerebral medullary substance, cerebellum, brain stem, hippocampus ileum, colon, rectum, ureter, aortopulmonary vessel and lymph-node. Real time RT-PCR evidence showed that matrix and hemagglutinin genes were positive in liver and spleen in addition to positive tissues with virus isolation. Immunohistochemistry and in-situ hybridization stains showed accordant evidence of viral infection with real time RT-PCR except bronchus. Quantitative RT-PCR suggested that a high viral load was associated with increased host responses, though the viral load was significantly different in various organs. Cells of the immunologic system could also be a target for virus infection. Overall, the pathogenesis of HPAI H5N1 virus was associated both with virus replication and with immunopathologic lesions. In addition, immune cells cannot be excluded from playing a role in dissemination of the virus in vivo. Public Library of Science 2010-10-12 /pmc/articles/PMC2953511/ /pubmed/20976271 http://dx.doi.org/10.1371/journal.pone.0013315 Text en Gao et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gao, Rongbao
Dong, Libo
Dong, Jie
Wen, Leying
Zhang, Ye
Yu, Hongjie
Feng, Zijian
Chen, Minmei
Tan, Yi
Mo, Zhaojun
Liu, Haiyan
Fan, Yunyan
Li, Kunxiong
Li, Chris Ka-Fai
Li, Dexin
Yang, Weizhong
Shu, Yuelong
A Systematic Molecular Pathology Study of a Laboratory Confirmed H5N1 Human Case
title A Systematic Molecular Pathology Study of a Laboratory Confirmed H5N1 Human Case
title_full A Systematic Molecular Pathology Study of a Laboratory Confirmed H5N1 Human Case
title_fullStr A Systematic Molecular Pathology Study of a Laboratory Confirmed H5N1 Human Case
title_full_unstemmed A Systematic Molecular Pathology Study of a Laboratory Confirmed H5N1 Human Case
title_short A Systematic Molecular Pathology Study of a Laboratory Confirmed H5N1 Human Case
title_sort systematic molecular pathology study of a laboratory confirmed h5n1 human case
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953511/
https://www.ncbi.nlm.nih.gov/pubmed/20976271
http://dx.doi.org/10.1371/journal.pone.0013315
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