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Fecal multi-omics analysis reveals diverse molecular alterations of gut ecosystem in COVID-19 patients
Gut ecosystem has profound effects on host physiology and health. Gastrointestinal (GI) symptoms were frequently observed in patients with COVID-19. Compared with other organs, gut antiviral response can result in more complicated immune responses because of the interactions between the gut microbio...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310733/ https://www.ncbi.nlm.nih.gov/pubmed/34538334 http://dx.doi.org/10.1016/j.aca.2021.338881 |
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author | He, Feixiang Zhang, Ting Xue, Kewen Fang, Zhaoxiong Jiang, Guanmin Huang, Siwen Li, Kexue Gu, Zhiqiang Shi, Honggang Zhang, Zhenyi Zhu, Huijin Lin, Lu Li, Jialin Xiao, Fei Shan, Hong Yan, Ru Li, Xiaofeng Yan, Zhixiang |
author_facet | He, Feixiang Zhang, Ting Xue, Kewen Fang, Zhaoxiong Jiang, Guanmin Huang, Siwen Li, Kexue Gu, Zhiqiang Shi, Honggang Zhang, Zhenyi Zhu, Huijin Lin, Lu Li, Jialin Xiao, Fei Shan, Hong Yan, Ru Li, Xiaofeng Yan, Zhixiang |
author_sort | He, Feixiang |
collection | PubMed |
description | Gut ecosystem has profound effects on host physiology and health. Gastrointestinal (GI) symptoms were frequently observed in patients with COVID-19. Compared with other organs, gut antiviral response can result in more complicated immune responses because of the interactions between the gut microbiota and host immunity. However, there are still large knowledge gaps in the impact of COVID-19 on gut molecular profiles and commensal microbiome, hindering our comprehensive understanding of the pathogenesis of SARS-CoV-2 and the treatment of COVID-19. We performed longitudinal stool multi-omics profiling to systemically investigate the molecular phenomics alterations of gut ecosystem in COVID-19. Gut proteomes of COVID-19 were characterized by disturbed immune, proteolysis and redox homeostasis. The expression and glycosylation of proteins involved in neutrophil degranulation and migration were suppressed, while those of proteases were upregulated. The variable domains of Ig heavy chains were downregulated and the overall glycosylation of IgA heavy chain constant regions, IgGFc-binding protein, and J chain were suppressed with glycan-specific variations. There was a reduction of beneficial gut bacteria and an enrichment of bacteria derived deleterious metabolites potentially associated with multiple types of diseases (such as ethyl glucuronide). The reduction of Ig heave chain variable domains may contribute to the increase of some Bacteroidetes species. Many bacteria ceramide lipids with a C17-sphingoid based were downregulated in COVID-19. In many cases, the gut phenome did not restore two months after symptom onset. Our study indicates widely disturbed gut molecular profiles which may play a role in the development of symptoms in COVID-19. Our findings also emphasis the need for ongoing investigation of the long-term gut molecular and microbial alterations during COVID-19 recovery process. Considering the gut ecosystem as a potential target could offer a valuable approach in managing the disease. |
format | Online Article Text |
id | pubmed-8310733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83107332021-07-26 Fecal multi-omics analysis reveals diverse molecular alterations of gut ecosystem in COVID-19 patients He, Feixiang Zhang, Ting Xue, Kewen Fang, Zhaoxiong Jiang, Guanmin Huang, Siwen Li, Kexue Gu, Zhiqiang Shi, Honggang Zhang, Zhenyi Zhu, Huijin Lin, Lu Li, Jialin Xiao, Fei Shan, Hong Yan, Ru Li, Xiaofeng Yan, Zhixiang Anal Chim Acta Article Gut ecosystem has profound effects on host physiology and health. Gastrointestinal (GI) symptoms were frequently observed in patients with COVID-19. Compared with other organs, gut antiviral response can result in more complicated immune responses because of the interactions between the gut microbiota and host immunity. However, there are still large knowledge gaps in the impact of COVID-19 on gut molecular profiles and commensal microbiome, hindering our comprehensive understanding of the pathogenesis of SARS-CoV-2 and the treatment of COVID-19. We performed longitudinal stool multi-omics profiling to systemically investigate the molecular phenomics alterations of gut ecosystem in COVID-19. Gut proteomes of COVID-19 were characterized by disturbed immune, proteolysis and redox homeostasis. The expression and glycosylation of proteins involved in neutrophil degranulation and migration were suppressed, while those of proteases were upregulated. The variable domains of Ig heavy chains were downregulated and the overall glycosylation of IgA heavy chain constant regions, IgGFc-binding protein, and J chain were suppressed with glycan-specific variations. There was a reduction of beneficial gut bacteria and an enrichment of bacteria derived deleterious metabolites potentially associated with multiple types of diseases (such as ethyl glucuronide). The reduction of Ig heave chain variable domains may contribute to the increase of some Bacteroidetes species. Many bacteria ceramide lipids with a C17-sphingoid based were downregulated in COVID-19. In many cases, the gut phenome did not restore two months after symptom onset. Our study indicates widely disturbed gut molecular profiles which may play a role in the development of symptoms in COVID-19. Our findings also emphasis the need for ongoing investigation of the long-term gut molecular and microbial alterations during COVID-19 recovery process. Considering the gut ecosystem as a potential target could offer a valuable approach in managing the disease. Published by Elsevier B.V. 2021-10-02 2021-07-26 /pmc/articles/PMC8310733/ /pubmed/34538334 http://dx.doi.org/10.1016/j.aca.2021.338881 Text en © 2021 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article He, Feixiang Zhang, Ting Xue, Kewen Fang, Zhaoxiong Jiang, Guanmin Huang, Siwen Li, Kexue Gu, Zhiqiang Shi, Honggang Zhang, Zhenyi Zhu, Huijin Lin, Lu Li, Jialin Xiao, Fei Shan, Hong Yan, Ru Li, Xiaofeng Yan, Zhixiang Fecal multi-omics analysis reveals diverse molecular alterations of gut ecosystem in COVID-19 patients |
title | Fecal multi-omics analysis reveals diverse molecular alterations of gut ecosystem in COVID-19 patients |
title_full | Fecal multi-omics analysis reveals diverse molecular alterations of gut ecosystem in COVID-19 patients |
title_fullStr | Fecal multi-omics analysis reveals diverse molecular alterations of gut ecosystem in COVID-19 patients |
title_full_unstemmed | Fecal multi-omics analysis reveals diverse molecular alterations of gut ecosystem in COVID-19 patients |
title_short | Fecal multi-omics analysis reveals diverse molecular alterations of gut ecosystem in COVID-19 patients |
title_sort | fecal multi-omics analysis reveals diverse molecular alterations of gut ecosystem in covid-19 patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310733/ https://www.ncbi.nlm.nih.gov/pubmed/34538334 http://dx.doi.org/10.1016/j.aca.2021.338881 |
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