Cargando…

Aggravated pneumonia and diabetes in SARS-CoV-2 infected diabetic mice

Multiple clinical and epidemiological studies have shown an interconnection between coronavirus disease 2019 (COVID-19) and diabetes, but experimental evidence is still lacking. Understanding the interplay between them is important because of the global health burden of COVID-19 and diabetes. We fou...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Qing, An, Ran, Wang, Haixuan, Yang, Yun, Tang, Cong, Wang, Junbin, Yu, Wenhai, Zhou, Yanan, Zhang, Yongmei, Wu, Daoju, Li, Bai, Yang, Hao, Lu, Shuaiyao, Peng, Xiaozhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155636/
https://www.ncbi.nlm.nih.gov/pubmed/37060137
http://dx.doi.org/10.1080/22221751.2023.2203782
_version_ 1785036372543799296
author Huang, Qing
An, Ran
Wang, Haixuan
Yang, Yun
Tang, Cong
Wang, Junbin
Yu, Wenhai
Zhou, Yanan
Zhang, Yongmei
Wu, Daoju
Li, Bai
Yang, Hao
Lu, Shuaiyao
Peng, Xiaozhong
author_facet Huang, Qing
An, Ran
Wang, Haixuan
Yang, Yun
Tang, Cong
Wang, Junbin
Yu, Wenhai
Zhou, Yanan
Zhang, Yongmei
Wu, Daoju
Li, Bai
Yang, Hao
Lu, Shuaiyao
Peng, Xiaozhong
author_sort Huang, Qing
collection PubMed
description Multiple clinical and epidemiological studies have shown an interconnection between coronavirus disease 2019 (COVID-19) and diabetes, but experimental evidence is still lacking. Understanding the interplay between them is important because of the global health burden of COVID-19 and diabetes. We found that C57BL/6J mice were susceptible to the alpha strain of SARS-CoV-2. Moreover, diabetic C57BL/6J mice with leptin receptor gene deficiency (db/db mice) showed a higher viral load in the throat and lung and slower virus clearance in the throat after infection than C57BL/6J mice. Histological and multifactor analysis revealed more advanced pulmonary injury and serum inflammation in SARS-CoV-2 infected diabetic mice. Moreover, SARS-CoV-2 infected diabetic mice exhibited more severe insulin resistance and islet cell loss than uninfected diabetic mice. By RNA sequencing analysis, we found that diabetes may reduce the collagen level, suppress the immune response and aggravate inflammation in the lung after infection, which may account for the greater susceptibility of diabetic mice and their more severe lung damage after infection. In summary, we successfully established a SARS-CoV-2 infected diabetic mice model and demonstrated that diabetes and COVID-19 were risk factors for one another.
format Online
Article
Text
id pubmed-10155636
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-101556362023-05-04 Aggravated pneumonia and diabetes in SARS-CoV-2 infected diabetic mice Huang, Qing An, Ran Wang, Haixuan Yang, Yun Tang, Cong Wang, Junbin Yu, Wenhai Zhou, Yanan Zhang, Yongmei Wu, Daoju Li, Bai Yang, Hao Lu, Shuaiyao Peng, Xiaozhong Emerg Microbes Infect Coronaviruses Multiple clinical and epidemiological studies have shown an interconnection between coronavirus disease 2019 (COVID-19) and diabetes, but experimental evidence is still lacking. Understanding the interplay between them is important because of the global health burden of COVID-19 and diabetes. We found that C57BL/6J mice were susceptible to the alpha strain of SARS-CoV-2. Moreover, diabetic C57BL/6J mice with leptin receptor gene deficiency (db/db mice) showed a higher viral load in the throat and lung and slower virus clearance in the throat after infection than C57BL/6J mice. Histological and multifactor analysis revealed more advanced pulmonary injury and serum inflammation in SARS-CoV-2 infected diabetic mice. Moreover, SARS-CoV-2 infected diabetic mice exhibited more severe insulin resistance and islet cell loss than uninfected diabetic mice. By RNA sequencing analysis, we found that diabetes may reduce the collagen level, suppress the immune response and aggravate inflammation in the lung after infection, which may account for the greater susceptibility of diabetic mice and their more severe lung damage after infection. In summary, we successfully established a SARS-CoV-2 infected diabetic mice model and demonstrated that diabetes and COVID-19 were risk factors for one another. Taylor & Francis 2023-05-01 /pmc/articles/PMC10155636/ /pubmed/37060137 http://dx.doi.org/10.1080/22221751.2023.2203782 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Coronaviruses
Huang, Qing
An, Ran
Wang, Haixuan
Yang, Yun
Tang, Cong
Wang, Junbin
Yu, Wenhai
Zhou, Yanan
Zhang, Yongmei
Wu, Daoju
Li, Bai
Yang, Hao
Lu, Shuaiyao
Peng, Xiaozhong
Aggravated pneumonia and diabetes in SARS-CoV-2 infected diabetic mice
title Aggravated pneumonia and diabetes in SARS-CoV-2 infected diabetic mice
title_full Aggravated pneumonia and diabetes in SARS-CoV-2 infected diabetic mice
title_fullStr Aggravated pneumonia and diabetes in SARS-CoV-2 infected diabetic mice
title_full_unstemmed Aggravated pneumonia and diabetes in SARS-CoV-2 infected diabetic mice
title_short Aggravated pneumonia and diabetes in SARS-CoV-2 infected diabetic mice
title_sort aggravated pneumonia and diabetes in sars-cov-2 infected diabetic mice
topic Coronaviruses
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155636/
https://www.ncbi.nlm.nih.gov/pubmed/37060137
http://dx.doi.org/10.1080/22221751.2023.2203782
work_keys_str_mv AT huangqing aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT anran aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT wanghaixuan aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT yangyun aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT tangcong aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT wangjunbin aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT yuwenhai aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT zhouyanan aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT zhangyongmei aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT wudaoju aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT libai aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT yanghao aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT lushuaiyao aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice
AT pengxiaozhong aggravatedpneumoniaanddiabetesinsarscov2infecteddiabeticmice