Proximity-ligation metagenomics reveals differential plasmid and chromosomal antimicrobial resistance gene carriage in disrupted gut ecosystems

Distinct ecological pressures shape accumulation of antimicrobial resistance genes (ARGs) and virulence genes in the gut microbiome. In this study, we used proximity ligation shotgun metagenomics to characterize bacterial host-mobilome relationships associated with antimicrobial resistance and virulence genes in two disease cohorts with microbiome dysbiosis: recurrent Clostridioides difficile infection (rCDI) and cirrhosis. Microbiome dysbiosis in patients with rCDI is primarily driven by prolonged antibiotic exposure, whereas dysbiosis in patients with cirrhosis results from altered gut physiology. We found an increased relative abundance of chromosomally linked antibiotic resistance determinants in both disease cohorts compared with healthy controls. The rCDI cohorts additionally exhibited increased relative abundance of plasmid-mediated ARGs.

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Journal
iScience
Published
2026-08-24
DOI
https://doi.org/10.1016/j.isci.2026.117312
Primary Topic
Clostridium difficile and Clostridium perfringens research
Type
article
Field-Weighted Citation Impact
0.00

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article

Proximity-ligation metagenomics reveals differential plasmid and chromosomal antimicrobial resistance gene carriage in disrupted gut ecosystems

Benjamin Auch, Andrew J. Sommer, Jasmohan Singh Bajaj, Alexander Khoruts
iScience
Clostridium difficile and Clostridium perfringens research
article

Proximity-ligation metagenomics reveals differential plasmid and chromosomal antimicrobial resistance gene carriage in disrupted gut ecosystems

Benjamin Auch, Andrew J. Sommer, Jasmohan Singh Bajaj, Alexander Khoruts
article en

Abstract

Distinct ecological pressures shape accumulation of antimicrobial resistance genes (ARGs) and virulence genes in the gut microbiome. In this study, we used proximity ligation shotgun metagenomics to characterize bacterial host-mobilome relationships associated with antimicrobial resistance and virulence genes in two disease cohorts with microbiome dysbiosis: recurrent Clostridioides difficile infection (rCDI) and cirrhosis. Microbiome dysbiosis in patients with rCDI is primarily driven by prolonged antibiotic exposure, whereas dysbiosis in patients with cirrhosis results from altered gut physiology. We found an increased relative abundance of chromosomally linked antibiotic resistance determinants in both disease cohorts compared with healthy controls. The rCDI cohorts additionally exhibited increased relative abundance of plasmid-mediated ARGs.

iScienceVol. 29(9)
University of Minnesota (US), ID Genomics (United States) (US), Virginia Commonwealth University Medical Center (US)
U.S. Department of Veterans Affairs, National Institute for Health and Care Research
Life in Land
Openalex Percentile: Top 10%
Clostridium difficile and Clostridium perfringens research
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