bioRxivMicrobiologyPreprint
Commensal taxa in gut microbiota limit antibiotic resistance during extended oral antibiotic use
Erika L. CyphertiD, Chongshan LiuiD, Victoria T. ChuiD, Aditi Dubey, Minying LiuiD, Zhe ZhongiD, James R. CockeyiD, Eva C. González DíaziD, Angie L. Morales, Jacob C. NixoniD, Matthew Garcia, Susana Zeng, Sidhant Rohatgi, Joan WongiD, Ritwicq ArjyaliD, Honey E. MekoneniD, Norma F NeffiD, Jennifer LeeiD, M. Kyla SheaiD, Xueyan FuiD, Sarah L. BoothiD, Cynthia Anne LeiferiD, Ankur K. SinghiD, Charles LangelieriD, Christopher J. HernandeziD
Abstract
Certain bacterial infections, such as those involving prosthetics, can require antimicrobial therapy over months to years, potentially increasing the burden of antimicrobial resistance. Here we longitudinally track the antimicrobial resistome in mice during continuous antibiotic dosing over 21 months. The burden of antibiotic resistance genes (ARGs) initially increases, but, surprisingly, declines in later months, approaching levels observed in untreated animals. ARG burden is regulated by taxonomy and declines as ARG-harboring taxa that initially bloom are replaced by commensals. Furthermore, we find that the dynamics of antibiotic-induced ARG burden are influenced by age-related differences in microbial taxonomy and can be removed by fecal microbiota transplantation. We show that commensals may regulate the resistome by limiting the growth of ARG-harboring taxa, thereby providing antimicrobial expansion resistance.
- organism: mouse
- assay: metagenomics
- research focus: host-pathogen & immune response
- approach: experimental assay
- Citations
- 1
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