4.8 Article

Acute and persistent effects of commonly used antibiotics on the gut microbiome and resistome in healthy adults

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CELL REPORTS
卷 39, 期 2, 页码 -

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CELL PRESS
DOI: 10.1016/j.celrep.2022.110649

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资金

  1. US Agency for International Development award [3220-29047]
  2. T32 NIH Ruth L. Kirschstein National Research Training Grant Fellowship [5T32GM007067-44]
  3. Society for Healthcare Epidemiology of America Research Scholar Award
  4. Institutional Program Unifying Population and Laboratory-Based Sciences
  5. Centers for Disease Control and Prevention [OADS BAA 2016-N-17812, 200-2016-90962]
  6. National Institute of Allergy and Infectious Diseases [1K23AI137321-01A1]

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This study quantitatively analyzed the dynamics of the gut microbiota in healthy adult volunteers before, during, and 6 months after receiving antibiotic treatment. The results showed that antibiotics led to changes in species diversity, resistome, and metabolic output, and delayed the recovery of species richness. A subset of volunteers experienced a persistent reduction in microbiome diversity after antibiotics.
Antibiotics are deployed against bacterial pathogens, but their targeting of conserved microbial processes means they also collaterally perturb the commensal microbiome. To understand acute and persistent effects of antibiotics on the gut microbiota of healthy adult volunteers, we quantify microbiome dynamics before, during, and 6 months after exposure to 4 commonly used antibiotic regimens. We observe an acute decrease in species richness and culturable bacteria after antibiotics, with most healthy adult microbiomes returning to pre-treatment species richness after 2 months, but with an altered taxonomy, resistome, and metabolic output, as well as an increased antibiotic resistance burden. Azithromycin delays the recovery of species richness, resulting in greater compositional distance. A subset of volunteers experience a persistent reduction in microbiome diversity after antibiotics and share compositional similarities with patients hospitalized in intensive care units. These results improve our quantitative understanding of the impact of antibiotics on commensal microbiome dynamics, resilience, and recovery.

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