<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nguyen LH</submitter><funding>NCATS NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>NCI</funding><funding>Mark and Lisa Schwartz</funding><funding>NHLBI NIH HHS</funding><funding>Crohn&amp;apos;s and Colitis Foundation</funding><funding>Massachusetts Consortium on Pathogen Readiness</funding><funding>NIDDK</funding><funding>American Gastroenterological Association</funding><pagination>49</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10337137</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The gut microbiome is a critical modulator of host immunity and is linked to the immune response to respiratory viral infections. However, few studies have gone beyond describing broad compositional alterations in severe COVID-19, defined as acute respiratory or other organ failure.&lt;h4>Methods&lt;/h4>We profiled 127 hospitalized patients with COVID-19 (n = 79 with severe COVID-19 and 48 with moderate) who collectively provided 241 stool samples from April 2020 to May 2021 to identify links between COVID-19 severity and gut microbial taxa, their biochemical pathways, and stool metabolites.&lt;h4>Results&lt;/h4>Forty-eight species were associated with severe disease after accounting for antibiotic use, age, sex, and various comorbidities. These included significant in-hospital depl</pubmed_abstract><journal>Genome medicine</journal><pubmed_title>Metagenomic assessment of gut microbial communities and risk of severe COVID-19.</pubmed_title><pmcid>PMC10337137</pmcid><funding_grant_id>2021-5102</funding_grant_id><funding_grant_id>K01 DK120742</funding_grant_id><funding_grant_id>K23 DK125838</funding_grant_id><funding_grant_id>UL1 TR002541</funding_grant_id><funding_grant_id>Research Fellowship Award</funding_grant_id><funding_grant_id>K23DK125838</funding_grant_id><funding_grant_id>Research Scholars Award</funding_grant_id><funding_grant_id>T32 HL116275</funding_grant_id><funding_grant_id>K01DK120742</funding_grant_id><funding_grant_id>Career Development Award</funding_grant_id><pubmed_authors>Reinicke T</pubmed_authors><pubmed_authors>Woo JE</pubmed_authors><pubmed_authors>Magicheva-Gupta M</pubmed_authors><pubmed_authors>Drew DA</pubmed_authors><pubmed_authors>Kim M</pubmed_authors><pubmed_authors>Lai PS</pubmed_authors><pubmed_authors>Jesudasen SJ</pubmed_authors><pubmed_authors>Thompson KN</pubmed_authors><pubmed_authors>Nguyen LH</pubmed_authors><pubmed_authors>McIver L</pubmed_authors><pubmed_authors>Okin D</pubmed_authors><pubmed_authors>Bhosle A</pubmed_authors><pubmed_authors>Lo CH</pubmed_authors><pubmed_authors>Caraballo A</pubmed_authors><pubmed_authors>Chan AT</pubmed_authors><pubmed_authors>Huttenhower C</pubmed_authors><pubmed_authors>Sui HY</pubmed_authors><pubmed_authors>Battista VM</pubmed_authors><pubmed_authors>Kuntz TM</pubmed_authors><pubmed_authors>Das Adhikari U</pubmed_authors><pubmed_authors>Goldberg MB</pubmed_authors><pubmed_authors>Kwon DS</pubmed_authors><pubmed_authors>Huang CY</pubmed_authors><pubmed_authors>Vieira J</pubmed_authors><pubmed_authors>Berra L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Metagenomic assessment of gut microbial communities and risk of severe COVID-19.</name><description>&lt;h4>Background&lt;/h4>The gut microbiome is a critical modulator of host immunity and is linked to the immune response to respiratory viral infections. However, few studies have gone beyond describing broad compositional alterations in severe COVID-19, defined as acute respiratory or other organ failure.&lt;h4>Methods&lt;/h4>We profiled 127 hospitalized patients with COVID-19 (n = 79 with severe COVID-19 and 48 with moderate) who collectively provided 241 stool samples from April 2020 to May 2021 to identify links between COVID-19 severity and gut microbial taxa, their biochemical pathways, and stool metabolites.&lt;h4>Results&lt;/h4>Forty-eight species were associated with severe disease after accounting for antibiotic use, age, sex, and various comorbidities. These included significant in-hospital depl</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jul</publication><modification>2025-07-12T03:06:18.158Z</modification><creation>2025-04-05T00:08:08.216Z</creation></dates><accession>S-EPMC10337137</accession><cross_references><pubmed>37438797</pubmed><doi>10.1186/s13073-023-01202-6</doi></cross_references></HashMap>