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SARS-CoV-2 infection reduces human nasopharyngeal commensal microbiome with inclusion of pathobionts

The microbiota of the nasopharyngeal tract (NT) play a role in host immunity against respiratory infectious diseases. However, scant information is available on interactions of SARS-CoV-2 with the nasopharyngeal microbiome. This study characterizes the effects of SARS-CoV-2 infection on human nasoph...

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Autores principales: Hoque, M. Nazmul, Sarkar, Md. Murshed Hasan, Rahman, M. Shaminur, Akter, Shahina, Banu, Tanjina Akhtar, Goswami, Barna, Jahan, Iffat, Hossain, M. Saddam, Shamsuzzaman, A. K. Mohammad, Nafisa, Tasnim, Molla, M. Maruf Ahmed, Yeasmin, Mahmuda, Ghosh, Asish Kumar, Osman, Eshrar, Alam, S. K. Saiful, Uzzaman, Mohammad Samir, Habib, Md Ahashan, Mahmud, Abu Sayeed Mohammad, Crandall, Keith A., Islam, Tofazzal, Khan, Md. Salim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674272/
https://www.ncbi.nlm.nih.gov/pubmed/34911967
http://dx.doi.org/10.1038/s41598-021-03245-4
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author Hoque, M. Nazmul
Sarkar, Md. Murshed Hasan
Rahman, M. Shaminur
Akter, Shahina
Banu, Tanjina Akhtar
Goswami, Barna
Jahan, Iffat
Hossain, M. Saddam
Shamsuzzaman, A. K. Mohammad
Nafisa, Tasnim
Molla, M. Maruf Ahmed
Yeasmin, Mahmuda
Ghosh, Asish Kumar
Osman, Eshrar
Alam, S. K. Saiful
Uzzaman, Mohammad Samir
Habib, Md Ahashan
Mahmud, Abu Sayeed Mohammad
Crandall, Keith A.
Islam, Tofazzal
Khan, Md. Salim
author_facet Hoque, M. Nazmul
Sarkar, Md. Murshed Hasan
Rahman, M. Shaminur
Akter, Shahina
Banu, Tanjina Akhtar
Goswami, Barna
Jahan, Iffat
Hossain, M. Saddam
Shamsuzzaman, A. K. Mohammad
Nafisa, Tasnim
Molla, M. Maruf Ahmed
Yeasmin, Mahmuda
Ghosh, Asish Kumar
Osman, Eshrar
Alam, S. K. Saiful
Uzzaman, Mohammad Samir
Habib, Md Ahashan
Mahmud, Abu Sayeed Mohammad
Crandall, Keith A.
Islam, Tofazzal
Khan, Md. Salim
author_sort Hoque, M. Nazmul
collection PubMed
description The microbiota of the nasopharyngeal tract (NT) play a role in host immunity against respiratory infectious diseases. However, scant information is available on interactions of SARS-CoV-2 with the nasopharyngeal microbiome. This study characterizes the effects of SARS-CoV-2 infection on human nasopharyngeal microbiomes and their relevant metabolic functions. Twenty-two (n = 22) nasopharyngeal swab samples (including COVID-19 patients = 8, recovered humans = 7, and healthy people = 7) were collected, and underwent to RNAseq-based metagenomic investigation. Our RNAseq data mapped to 2281 bacterial species (including 1477, 919 and 676 in healthy, COVID-19 and recovered metagenomes, respectively) indicating a distinct microbiome dysbiosis. The COVID-19 and recovered samples included 67% and 77% opportunistic bacterial species, respectively compared to healthy controls. Notably, 79% commensal bacterial species found in healthy controls were not detected in COVID-19 and recovered people. Similar dysbiosis was also found in viral and archaeal fraction of the nasopharyngeal microbiomes. We also detected several altered metabolic pathways and functional genes in the progression and pathophysiology of COVID-19. The nasopharyngeal microbiome dysbiosis and their genomic features determined by our RNAseq analyses shed light on early interactions of SARS-CoV-2 with the nasopharyngeal resident microbiota that might be helpful for developing microbiome-based diagnostics and therapeutics for this novel pandemic disease.
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spelling pubmed-86742722021-12-16 SARS-CoV-2 infection reduces human nasopharyngeal commensal microbiome with inclusion of pathobionts Hoque, M. Nazmul Sarkar, Md. Murshed Hasan Rahman, M. Shaminur Akter, Shahina Banu, Tanjina Akhtar Goswami, Barna Jahan, Iffat Hossain, M. Saddam Shamsuzzaman, A. K. Mohammad Nafisa, Tasnim Molla, M. Maruf Ahmed Yeasmin, Mahmuda Ghosh, Asish Kumar Osman, Eshrar Alam, S. K. Saiful Uzzaman, Mohammad Samir Habib, Md Ahashan Mahmud, Abu Sayeed Mohammad Crandall, Keith A. Islam, Tofazzal Khan, Md. Salim Sci Rep Article The microbiota of the nasopharyngeal tract (NT) play a role in host immunity against respiratory infectious diseases. However, scant information is available on interactions of SARS-CoV-2 with the nasopharyngeal microbiome. This study characterizes the effects of SARS-CoV-2 infection on human nasopharyngeal microbiomes and their relevant metabolic functions. Twenty-two (n = 22) nasopharyngeal swab samples (including COVID-19 patients = 8, recovered humans = 7, and healthy people = 7) were collected, and underwent to RNAseq-based metagenomic investigation. Our RNAseq data mapped to 2281 bacterial species (including 1477, 919 and 676 in healthy, COVID-19 and recovered metagenomes, respectively) indicating a distinct microbiome dysbiosis. The COVID-19 and recovered samples included 67% and 77% opportunistic bacterial species, respectively compared to healthy controls. Notably, 79% commensal bacterial species found in healthy controls were not detected in COVID-19 and recovered people. Similar dysbiosis was also found in viral and archaeal fraction of the nasopharyngeal microbiomes. We also detected several altered metabolic pathways and functional genes in the progression and pathophysiology of COVID-19. The nasopharyngeal microbiome dysbiosis and their genomic features determined by our RNAseq analyses shed light on early interactions of SARS-CoV-2 with the nasopharyngeal resident microbiota that might be helpful for developing microbiome-based diagnostics and therapeutics for this novel pandemic disease. Nature Publishing Group UK 2021-12-15 /pmc/articles/PMC8674272/ /pubmed/34911967 http://dx.doi.org/10.1038/s41598-021-03245-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hoque, M. Nazmul
Sarkar, Md. Murshed Hasan
Rahman, M. Shaminur
Akter, Shahina
Banu, Tanjina Akhtar
Goswami, Barna
Jahan, Iffat
Hossain, M. Saddam
Shamsuzzaman, A. K. Mohammad
Nafisa, Tasnim
Molla, M. Maruf Ahmed
Yeasmin, Mahmuda
Ghosh, Asish Kumar
Osman, Eshrar
Alam, S. K. Saiful
Uzzaman, Mohammad Samir
Habib, Md Ahashan
Mahmud, Abu Sayeed Mohammad
Crandall, Keith A.
Islam, Tofazzal
Khan, Md. Salim
SARS-CoV-2 infection reduces human nasopharyngeal commensal microbiome with inclusion of pathobionts
title SARS-CoV-2 infection reduces human nasopharyngeal commensal microbiome with inclusion of pathobionts
title_full SARS-CoV-2 infection reduces human nasopharyngeal commensal microbiome with inclusion of pathobionts
title_fullStr SARS-CoV-2 infection reduces human nasopharyngeal commensal microbiome with inclusion of pathobionts
title_full_unstemmed SARS-CoV-2 infection reduces human nasopharyngeal commensal microbiome with inclusion of pathobionts
title_short SARS-CoV-2 infection reduces human nasopharyngeal commensal microbiome with inclusion of pathobionts
title_sort sars-cov-2 infection reduces human nasopharyngeal commensal microbiome with inclusion of pathobionts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674272/
https://www.ncbi.nlm.nih.gov/pubmed/34911967
http://dx.doi.org/10.1038/s41598-021-03245-4
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