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H1N1 exposure during the convalescent stage of SARS-CoV-2 infection results in enhanced lung pathologic damage in hACE2 transgenic mice
The risk of secondary infection with SARS-CoV-2 and influenza A virus is becoming a practical problem that must be addressed as the flu season merges with the COVID-19 pandemic. As SARS-CoV-2 and influenza A virus have been found in patients, understanding the in vivo characteristics of the secondar...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8205102/ https://www.ncbi.nlm.nih.gov/pubmed/34060982 http://dx.doi.org/10.1080/22221751.2021.1938241 |
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author | Li, Heng Zhao, Xin Zhao, Yurong Li, Jing Zheng, Huiwen Xue, Mengyi Guo, Lei Zhou, Jian Yang, Jinling Zuo, Yuanyuan Chen, Yanli Yang, Zening Fan, Qiqi Qin, Li Shi, Haijing Liu, Longding |
author_facet | Li, Heng Zhao, Xin Zhao, Yurong Li, Jing Zheng, Huiwen Xue, Mengyi Guo, Lei Zhou, Jian Yang, Jinling Zuo, Yuanyuan Chen, Yanli Yang, Zening Fan, Qiqi Qin, Li Shi, Haijing Liu, Longding |
author_sort | Li, Heng |
collection | PubMed |
description | The risk of secondary infection with SARS-CoV-2 and influenza A virus is becoming a practical problem that must be addressed as the flu season merges with the COVID-19 pandemic. As SARS-CoV-2 and influenza A virus have been found in patients, understanding the in vivo characteristics of the secondary infection between these two viruses is a high priority. Here, hACE2 transgenic mice were challenged with the H1N1 virus at a nonlethal dose during the convalescent stage on 7 and 14 days post SARS-CoV-2 infection, and importantly, subsequent H1N1 infection showed enhanced viral shedding and virus tissue distribution. Histopathological observation revealed an extensive pathological change in the lungs related to H1N1 infection in mice recovered from SARS-CoV-2 infection, with severe inflammation infiltration and bronchiole disruption. Moreover, upon H1N1 exposure on 7 and 14 dpi of SARS-CoV-2 infection, the lymphocyte population activated at a lower level with T cell suppressed in both PBMC and lung. These findings will be valuable for evaluating antiviral therapeutics and vaccines as well as guiding public health work. |
format | Online Article Text |
id | pubmed-8205102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-82051022021-06-24 H1N1 exposure during the convalescent stage of SARS-CoV-2 infection results in enhanced lung pathologic damage in hACE2 transgenic mice Li, Heng Zhao, Xin Zhao, Yurong Li, Jing Zheng, Huiwen Xue, Mengyi Guo, Lei Zhou, Jian Yang, Jinling Zuo, Yuanyuan Chen, Yanli Yang, Zening Fan, Qiqi Qin, Li Shi, Haijing Liu, Longding Emerg Microbes Infect Research Article The risk of secondary infection with SARS-CoV-2 and influenza A virus is becoming a practical problem that must be addressed as the flu season merges with the COVID-19 pandemic. As SARS-CoV-2 and influenza A virus have been found in patients, understanding the in vivo characteristics of the secondary infection between these two viruses is a high priority. Here, hACE2 transgenic mice were challenged with the H1N1 virus at a nonlethal dose during the convalescent stage on 7 and 14 days post SARS-CoV-2 infection, and importantly, subsequent H1N1 infection showed enhanced viral shedding and virus tissue distribution. Histopathological observation revealed an extensive pathological change in the lungs related to H1N1 infection in mice recovered from SARS-CoV-2 infection, with severe inflammation infiltration and bronchiole disruption. Moreover, upon H1N1 exposure on 7 and 14 dpi of SARS-CoV-2 infection, the lymphocyte population activated at a lower level with T cell suppressed in both PBMC and lung. These findings will be valuable for evaluating antiviral therapeutics and vaccines as well as guiding public health work. Taylor & Francis 2021-06-13 /pmc/articles/PMC8205102/ /pubmed/34060982 http://dx.doi.org/10.1080/22221751.2021.1938241 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Li, Heng Zhao, Xin Zhao, Yurong Li, Jing Zheng, Huiwen Xue, Mengyi Guo, Lei Zhou, Jian Yang, Jinling Zuo, Yuanyuan Chen, Yanli Yang, Zening Fan, Qiqi Qin, Li Shi, Haijing Liu, Longding H1N1 exposure during the convalescent stage of SARS-CoV-2 infection results in enhanced lung pathologic damage in hACE2 transgenic mice |
title | H1N1 exposure during the convalescent stage of SARS-CoV-2 infection results in enhanced lung pathologic damage in hACE2 transgenic mice |
title_full | H1N1 exposure during the convalescent stage of SARS-CoV-2 infection results in enhanced lung pathologic damage in hACE2 transgenic mice |
title_fullStr | H1N1 exposure during the convalescent stage of SARS-CoV-2 infection results in enhanced lung pathologic damage in hACE2 transgenic mice |
title_full_unstemmed | H1N1 exposure during the convalescent stage of SARS-CoV-2 infection results in enhanced lung pathologic damage in hACE2 transgenic mice |
title_short | H1N1 exposure during the convalescent stage of SARS-CoV-2 infection results in enhanced lung pathologic damage in hACE2 transgenic mice |
title_sort | h1n1 exposure during the convalescent stage of sars-cov-2 infection results in enhanced lung pathologic damage in hace2 transgenic mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8205102/ https://www.ncbi.nlm.nih.gov/pubmed/34060982 http://dx.doi.org/10.1080/22221751.2021.1938241 |
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