Gut microbiome alpha diversity decreases in relation to body weight, antibiotic exposure, and infection with multidrug-resistant organisms
The human gastrointestinal tract is home to a dense and diverse microbiome, predominated by bacteria. Despite the conservation of critical functionality across most individuals, the composition of the gut microbiome is highly individualized, leading to differential responses to perturbations such as...
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Published in | American journal of infection control Vol. 52; no. 6; pp. 707 - 711 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.06.2024
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Subjects | |
Online Access | Get full text |
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Summary: | The human gastrointestinal tract is home to a dense and diverse microbiome, predominated by bacteria. Despite the conservation of critical functionality across most individuals, the composition of the gut microbiome is highly individualized, leading to differential responses to perturbations such as oral antibiotics or multidrug-resistant organism (MDRO) infection. Herein, subject responses to these perturbations based on their body weight were evaluated.
Fecal samples were collected from 45 subjects at the Detroit Medical Center to evaluate the effects of perturbations on subjects’ gut microbiome composition. Bacterial profiling was completed using 16S rRNA gene sequencing.
Subjects with multiple MDROs, subjects weighing greater than 80 kg infected with MDRO E coli, and subjects weighing less than 80 kg with exposure to vancomycin and carbapenem antibiotics during hospitalization had significantly decreased gut microbiome richness.
Both administration of oral antibiotics and MDRO infections decreased gut microbiome alpha diversity, but the magnitude of these gut microbiome perturbations was body weight dependent.
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•Subjects with more MDRO infections had decreased gut microbiome richness.•High-weight subjects with MDRO E. coli had decreased gut microbiome richness.•Low-weight subjects had decreased gut microbiome richness with antibiotics. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0196-6553 1527-3296 1527-3296 |
DOI: | 10.1016/j.ajic.2023.12.017 |