Impact of Amoxicillin-Clavulanate followed by Autologous Fecal Microbiota Transplantation on Fecal Microbiome Structure and Metabolic Potential

Author:

Bulow Christopher1ORCID,Langdon Amy1,Hink Tiffany2,Wallace Meghan3,Reske Kimberly A.2,Patel Sanket1,Sun Xiaoqing1,Seiler Sondra2,Jones Susan4,Kwon Jennie H.2,Burnham Carey-Ann D.356ORCID,Dantas Gautam1357,Dubberke Erik R.2

Affiliation:

1. The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, Missouri, USA

2. Division of Infectious Diseases, Washington University School of Medicine, St. Louis, Missouri, USA

3. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA

4. Division of Gastroenterology, Washington University School of Medicine, St. Louis, Missouri, USA

5. Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, USA

6. Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA

7. Department of Biomedical Engineering, Washington University School of Medicine, St. Louis, Missouri, USA

Abstract

The spread of multidrug resistance among pathogenic organisms threatens the efficacy of antimicrobial treatment options. The human gut serves as a reservoir for many drug-resistant organisms and their resistance genes, and perturbation of the gut microbiome by antimicrobial exposure can open metabolic niches to resistant pathogens. Once established in the gut, antimicrobial-resistant bacteria can persist even after antimicrobial exposure ceases. Strategies to prevent multidrug-resistant organism (MDRO) infections are scarce, but autologous fecal microbiota transplantation (autoFMT) may limit gastrointestinal MDRO expansion. AutoFMT involves banking one’s feces during a healthy state for later use in restoring gut microbiota following perturbation. This pilot study evaluated the effect of amoxicillin-clavulanic acid (Amox-Clav) exposure and autoFMT on gastrointestinal microbiome taxonomic composition, resistance gene content, and metabolic capacity. Importantly, we found that metabolic capacity was perturbed even in cases where gross phylogeny remained unchanged and that autoFMT was safe and well tolerated.

Funder

HHS | National Institutes of Health

HHS | NIH | National Human Genome Research Institute

HHS | NIH | National Center for Advancing Translational Sciences

HHS | Centers for Disease Control and Prevention

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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