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Gut microbiota in antiviral strategy from bats to humans: a missing link in COVID-19

Bats are a potential natural reservoir for SARS-CoV-2 virus and other viruses detrimental to humans. Accumulated evidence has shown that, in their adaptation to a flight-based lifestyle, remodeling of the gut microbiota in bats may have contributed to immune tolerance to viruses. This evidence from...

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Detalles Bibliográficos
Autores principales: Luo, Jia, Liang, Shan, Jin, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Science China Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847806/
https://www.ncbi.nlm.nih.gov/pubmed/33521857
http://dx.doi.org/10.1007/s11427-020-1847-7
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author Luo, Jia
Liang, Shan
Jin, Feng
author_facet Luo, Jia
Liang, Shan
Jin, Feng
author_sort Luo, Jia
collection PubMed
description Bats are a potential natural reservoir for SARS-CoV-2 virus and other viruses detrimental to humans. Accumulated evidence has shown that, in their adaptation to a flight-based lifestyle, remodeling of the gut microbiota in bats may have contributed to immune tolerance to viruses. This evidence from bats provides profound insights into the potential influence of gut microbiota in COVID-19 disease in humans. Here, we highlight recent advances in our understanding of the mechanisms by which the gut microbiota helps bats tolerate deadly viruses, and summarize the current clinical evidence on the influence of gut microbiota on the susceptibility to SARS-CoV-2 infection and risk of COVID-19 leading to a fatal outcome. In addition, we discuss the implications of gut microbiota-targeted approaches for preventing infection and reducing disease severity in COVID-19 patients.
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spelling pubmed-78478062021-02-01 Gut microbiota in antiviral strategy from bats to humans: a missing link in COVID-19 Luo, Jia Liang, Shan Jin, Feng Sci China Life Sci Review Bats are a potential natural reservoir for SARS-CoV-2 virus and other viruses detrimental to humans. Accumulated evidence has shown that, in their adaptation to a flight-based lifestyle, remodeling of the gut microbiota in bats may have contributed to immune tolerance to viruses. This evidence from bats provides profound insights into the potential influence of gut microbiota in COVID-19 disease in humans. Here, we highlight recent advances in our understanding of the mechanisms by which the gut microbiota helps bats tolerate deadly viruses, and summarize the current clinical evidence on the influence of gut microbiota on the susceptibility to SARS-CoV-2 infection and risk of COVID-19 leading to a fatal outcome. In addition, we discuss the implications of gut microbiota-targeted approaches for preventing infection and reducing disease severity in COVID-19 patients. Science China Press 2021-01-27 2021 /pmc/articles/PMC7847806/ /pubmed/33521857 http://dx.doi.org/10.1007/s11427-020-1847-7 Text en © Science China Press and Springer-Verlag GmbH Germany, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review
Luo, Jia
Liang, Shan
Jin, Feng
Gut microbiota in antiviral strategy from bats to humans: a missing link in COVID-19
title Gut microbiota in antiviral strategy from bats to humans: a missing link in COVID-19
title_full Gut microbiota in antiviral strategy from bats to humans: a missing link in COVID-19
title_fullStr Gut microbiota in antiviral strategy from bats to humans: a missing link in COVID-19
title_full_unstemmed Gut microbiota in antiviral strategy from bats to humans: a missing link in COVID-19
title_short Gut microbiota in antiviral strategy from bats to humans: a missing link in COVID-19
title_sort gut microbiota in antiviral strategy from bats to humans: a missing link in covid-19
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847806/
https://www.ncbi.nlm.nih.gov/pubmed/33521857
http://dx.doi.org/10.1007/s11427-020-1847-7
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