The gut microbiome of COVID-19 recovered patients returns to uninfected status in a minority-dominated United States cohort
To investigate the relationship between intestinal microbiota and SARS-CoV-2-mediated pathogenicity in a United States, majority African American cohort. We prospectively collected fecal samples from 50 SARS-CoV-2 infected patients, 9 SARS-CoV-2 recovered patients, and 34 uninfected subjects seen by...
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doaj-96685b2fdf614995a7d3332aa38157fb2021-07-06T12:16:09ZengTaylor & Francis GroupGut Microbes1949-09761949-09842021-01-0113110.1080/19490976.2021.19268401926840The gut microbiome of COVID-19 recovered patients returns to uninfected status in a minority-dominated United States cohortRachel C. Newsome0Josee Gauthier1Maria C. Hernandez2George E. Abraham3Tanya O. Robinson4Haley B. Williams5Meredith Sloan6Anna Owings7Hannah Laird8Taylor Christian9Yilianys Pride10Kenneth J. Wilson11Mohammad Hasan12Adam Parker13Michal Senitko14Sarah C. Glover15Raad Z. Gharaibeh16Christian Jobin17University of Florida College of MedicineUniversity of Florida College of MedicineUniversity of Florida College of MedicineUniversity of Mississippi Medical CenterUniversity of Mississippi Medical CenterUniversity of Mississippi Medical CenterUniversity of Mississippi Medical CenterUniversity of Mississippi Medical CenterUniversity of Mississippi Medical CenterUniversity of Mississippi Medical CenterUniversity of Mississippi Medical CenterUniversity of Mississippi Medical CenterUniversity of Mississippi Medical CenterUniversity of Mississippi Medical CenterUniversity of Mississippi Medical CenterUniversity of Florida College of MedicineUniversity of Florida College of MedicineUniversity of Florida College of MedicineTo investigate the relationship between intestinal microbiota and SARS-CoV-2-mediated pathogenicity in a United States, majority African American cohort. We prospectively collected fecal samples from 50 SARS-CoV-2 infected patients, 9 SARS-CoV-2 recovered patients, and 34 uninfected subjects seen by the hospital with unrelated respiratory medical conditions (controls). 16S rRNA sequencing and qPCR analysis was performed on fecal DNA/RNA. The fecal microbial composition was found to be significantly different between SARS-CoV-2 patients and controls (PERMANOVA FDR-P = .004), independent of antibiotic exposure. Peptoniphilus, Corynebacterium and Campylobacter were identified as the three most significantly enriched genera in COVID-19 patients compared to controls. Actively infected patients were also found to have a different gut microbiota than recovered patients (PERMANOVA FDR-P = .003), and the most enriched genus in infected patients was Campylobacter, with Agathobacter and Faecalibacterium being enriched in the recovered patients. No difference in microbial community structure between recovered patients and uninfected controls was observed, nor a difference in alpha diversity between the three groups. 24 of the 50 COVID-19 patients (48%) tested positive via RT-qPCR for fecal SARS-CoV-2 RNA. A significant difference in gut microbial composition between SARS-CoV-2 positive and negative samples was observed, with Klebsiella and Agathobacter being enriched in the positive cohort. No significant associations between microbiome composition and disease severity was found. The intestinal microbiota is sensitive to the presence of SARS-CoV-2, with increased relative abundance of genera (Campylobacter, Klebsiella) associated with gastrointestinal (GI) disease. Further studies are needed to investigate the functional impact of SARS-CoV-2 on GI health.http://dx.doi.org/10.1080/19490976.2021.1926840human gut microbiotasars-cov-216s rrna sequencingclinical studymicrobiomemicrobiotacovid-19 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rachel C. Newsome Josee Gauthier Maria C. Hernandez George E. Abraham Tanya O. Robinson Haley B. Williams Meredith Sloan Anna Owings Hannah Laird Taylor Christian Yilianys Pride Kenneth J. Wilson Mohammad Hasan Adam Parker Michal Senitko Sarah C. Glover Raad Z. Gharaibeh Christian Jobin |
spellingShingle |
Rachel C. Newsome Josee Gauthier Maria C. Hernandez George E. Abraham Tanya O. Robinson Haley B. Williams Meredith Sloan Anna Owings Hannah Laird Taylor Christian Yilianys Pride Kenneth J. Wilson Mohammad Hasan Adam Parker Michal Senitko Sarah C. Glover Raad Z. Gharaibeh Christian Jobin The gut microbiome of COVID-19 recovered patients returns to uninfected status in a minority-dominated United States cohort Gut Microbes human gut microbiota sars-cov-2 16s rrna sequencing clinical study microbiome microbiota covid-19 |
author_facet |
Rachel C. Newsome Josee Gauthier Maria C. Hernandez George E. Abraham Tanya O. Robinson Haley B. Williams Meredith Sloan Anna Owings Hannah Laird Taylor Christian Yilianys Pride Kenneth J. Wilson Mohammad Hasan Adam Parker Michal Senitko Sarah C. Glover Raad Z. Gharaibeh Christian Jobin |
author_sort |
Rachel C. Newsome |
title |
The gut microbiome of COVID-19 recovered patients returns to uninfected status in a minority-dominated United States cohort |
title_short |
The gut microbiome of COVID-19 recovered patients returns to uninfected status in a minority-dominated United States cohort |
title_full |
The gut microbiome of COVID-19 recovered patients returns to uninfected status in a minority-dominated United States cohort |
title_fullStr |
The gut microbiome of COVID-19 recovered patients returns to uninfected status in a minority-dominated United States cohort |
title_full_unstemmed |
The gut microbiome of COVID-19 recovered patients returns to uninfected status in a minority-dominated United States cohort |
title_sort |
gut microbiome of covid-19 recovered patients returns to uninfected status in a minority-dominated united states cohort |
publisher |
Taylor & Francis Group |
series |
Gut Microbes |
issn |
1949-0976 1949-0984 |
publishDate |
2021-01-01 |
description |
To investigate the relationship between intestinal microbiota and SARS-CoV-2-mediated pathogenicity in a United States, majority African American cohort. We prospectively collected fecal samples from 50 SARS-CoV-2 infected patients, 9 SARS-CoV-2 recovered patients, and 34 uninfected subjects seen by the hospital with unrelated respiratory medical conditions (controls). 16S rRNA sequencing and qPCR analysis was performed on fecal DNA/RNA. The fecal microbial composition was found to be significantly different between SARS-CoV-2 patients and controls (PERMANOVA FDR-P = .004), independent of antibiotic exposure. Peptoniphilus, Corynebacterium and Campylobacter were identified as the three most significantly enriched genera in COVID-19 patients compared to controls. Actively infected patients were also found to have a different gut microbiota than recovered patients (PERMANOVA FDR-P = .003), and the most enriched genus in infected patients was Campylobacter, with Agathobacter and Faecalibacterium being enriched in the recovered patients. No difference in microbial community structure between recovered patients and uninfected controls was observed, nor a difference in alpha diversity between the three groups. 24 of the 50 COVID-19 patients (48%) tested positive via RT-qPCR for fecal SARS-CoV-2 RNA. A significant difference in gut microbial composition between SARS-CoV-2 positive and negative samples was observed, with Klebsiella and Agathobacter being enriched in the positive cohort. No significant associations between microbiome composition and disease severity was found. The intestinal microbiota is sensitive to the presence of SARS-CoV-2, with increased relative abundance of genera (Campylobacter, Klebsiella) associated with gastrointestinal (GI) disease. Further studies are needed to investigate the functional impact of SARS-CoV-2 on GI health. |
topic |
human gut microbiota sars-cov-2 16s rrna sequencing clinical study microbiome microbiota covid-19 |
url |
http://dx.doi.org/10.1080/19490976.2021.1926840 |
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