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Enriched Opportunistic Pathogens Revealed by Metagenomic Sequencing Hint Potential Linkages between Pharyngeal Microbiota and COVID-19

As a respiratory tract virus, SARS-CoV-2 infected people through contacting with the upper respiratory tract first. Previous studies indicated that microbiota could modulate immune response against pathogen infection. In the present study, we performed metagenomic sequencing of pharyngeal swabs from...

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Autores principales: Xiong, Dongyan, Muema, Caroline, Zhang, Xiaoxu, Pan, Xinming, Xiong, Jin, Yang, Hang, Yu, Junping, Wei, Hongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114661/
https://www.ncbi.nlm.nih.gov/pubmed/33978940
http://dx.doi.org/10.1007/s12250-021-00391-x
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author Xiong, Dongyan
Muema, Caroline
Zhang, Xiaoxu
Pan, Xinming
Xiong, Jin
Yang, Hang
Yu, Junping
Wei, Hongping
author_facet Xiong, Dongyan
Muema, Caroline
Zhang, Xiaoxu
Pan, Xinming
Xiong, Jin
Yang, Hang
Yu, Junping
Wei, Hongping
author_sort Xiong, Dongyan
collection PubMed
description As a respiratory tract virus, SARS-CoV-2 infected people through contacting with the upper respiratory tract first. Previous studies indicated that microbiota could modulate immune response against pathogen infection. In the present study, we performed metagenomic sequencing of pharyngeal swabs from eleven patients with COVID-19 and eleven Non-COVID-19 patients who had similar symptoms such as fever and cough. Through metagenomic analysis of the above two groups and a healthy group from the public data, there are 6502 species identified in the samples. Specifically, the Pielou index indicated a lower evenness of the microbiota in the COVID-19 group than that in the Non-COVID-19 group. Combined with the linear discriminant analysis (LDA) and the generalized linear model, eighty-one bacterial species were found with increased abundance in the COVID-19 group, where 51 species were enriched more than 8 folds. The top three enriched genera were Streptococcus, Prevotella and Campylobacter containing some opportunistic pathogens. More interestingly, through experiments, we found that two Streptococcus strains, S. suis and S. agalactiae, could stimulate the expression of ACE2 of Vero cells in vitro, which may promote SARS-CoV-2 infection. Therefore, these enriched pathogens in the pharynxes of COVID-19 patients may involve in the virus-host interactions to affect SARS-CoV-2 infection and cause potential secondary bacterial infections through changing the expression of the viral receptor ACE2 and/or modulate the host’s immune system. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12250-021-00391-x.
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spelling pubmed-81146612021-05-12 Enriched Opportunistic Pathogens Revealed by Metagenomic Sequencing Hint Potential Linkages between Pharyngeal Microbiota and COVID-19 Xiong, Dongyan Muema, Caroline Zhang, Xiaoxu Pan, Xinming Xiong, Jin Yang, Hang Yu, Junping Wei, Hongping Virol Sin Research Article As a respiratory tract virus, SARS-CoV-2 infected people through contacting with the upper respiratory tract first. Previous studies indicated that microbiota could modulate immune response against pathogen infection. In the present study, we performed metagenomic sequencing of pharyngeal swabs from eleven patients with COVID-19 and eleven Non-COVID-19 patients who had similar symptoms such as fever and cough. Through metagenomic analysis of the above two groups and a healthy group from the public data, there are 6502 species identified in the samples. Specifically, the Pielou index indicated a lower evenness of the microbiota in the COVID-19 group than that in the Non-COVID-19 group. Combined with the linear discriminant analysis (LDA) and the generalized linear model, eighty-one bacterial species were found with increased abundance in the COVID-19 group, where 51 species were enriched more than 8 folds. The top three enriched genera were Streptococcus, Prevotella and Campylobacter containing some opportunistic pathogens. More interestingly, through experiments, we found that two Streptococcus strains, S. suis and S. agalactiae, could stimulate the expression of ACE2 of Vero cells in vitro, which may promote SARS-CoV-2 infection. Therefore, these enriched pathogens in the pharynxes of COVID-19 patients may involve in the virus-host interactions to affect SARS-CoV-2 infection and cause potential secondary bacterial infections through changing the expression of the viral receptor ACE2 and/or modulate the host’s immune system. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12250-021-00391-x. Springer Singapore 2021-05-12 /pmc/articles/PMC8114661/ /pubmed/33978940 http://dx.doi.org/10.1007/s12250-021-00391-x Text en © Wuhan Institute of Virology, CAS 2021
spellingShingle Research Article
Xiong, Dongyan
Muema, Caroline
Zhang, Xiaoxu
Pan, Xinming
Xiong, Jin
Yang, Hang
Yu, Junping
Wei, Hongping
Enriched Opportunistic Pathogens Revealed by Metagenomic Sequencing Hint Potential Linkages between Pharyngeal Microbiota and COVID-19
title Enriched Opportunistic Pathogens Revealed by Metagenomic Sequencing Hint Potential Linkages between Pharyngeal Microbiota and COVID-19
title_full Enriched Opportunistic Pathogens Revealed by Metagenomic Sequencing Hint Potential Linkages between Pharyngeal Microbiota and COVID-19
title_fullStr Enriched Opportunistic Pathogens Revealed by Metagenomic Sequencing Hint Potential Linkages between Pharyngeal Microbiota and COVID-19
title_full_unstemmed Enriched Opportunistic Pathogens Revealed by Metagenomic Sequencing Hint Potential Linkages between Pharyngeal Microbiota and COVID-19
title_short Enriched Opportunistic Pathogens Revealed by Metagenomic Sequencing Hint Potential Linkages between Pharyngeal Microbiota and COVID-19
title_sort enriched opportunistic pathogens revealed by metagenomic sequencing hint potential linkages between pharyngeal microbiota and covid-19
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114661/
https://www.ncbi.nlm.nih.gov/pubmed/33978940
http://dx.doi.org/10.1007/s12250-021-00391-x
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