Fecal microbiota transplantation promotes reduction of antimicrobial resistance by strain replacement

殖民抵抗 某种肠道细菌 粪便 微生物群 医学 普氏粪杆菌 移植 微生物学 随机对照试验 内科学 生物 殖民地化 胃肠病学 免疫学 肠道菌群 生物信息学
作者
Michael H. Woodworth,Roth E. Conrad,Marina E Haldopoulos,Stephanie M. Pouch,Ahmed Babiker,Aneesh K. Mehta,Kaitlin L. Sitchenko,Charlotte H. Wang,Amanda F Strudwick,Jessica Ingersoll,Cécile Philippe,Sarah Lohsen,Kumru Kocaman,Blake G. Lindner,Janet K. Hatt,Rheinallt Jones,Candace Miller,Andrew S. Neish,Rachel Friedman‐Moraco,Geeta Karadkhele,Ken Liu,Dean P. Jones,C. Christina Mehta,Thomas R. Ziegler,David S. Weiss,Christian Larsen,Konstantinos T. Konstantinidis,Colleen S. Kraft
出处
期刊:Science Translational Medicine [American Association for the Advancement of Science (AAAS)]
卷期号:15 (720) 被引量:10
标识
DOI:10.1126/scitranslmed.abo2750
摘要

Multidrug-resistant organism (MDRO) colonization is a fundamental challenge in antimicrobial resistance. Limited studies have shown that fecal microbiota transplantation (FMT) can reduce MDRO colonization, but its mechanisms are poorly understood. We conducted a randomized, controlled trial of FMT for MDRO decolonization in renal transplant recipients called PREMIX (NCT02922816). Eleven participants were enrolled and randomized 1:1 to FMT or an observation period followed by delayed FMT if stool cultures were MDRO positive at day 36. Participants who were MDRO positive after one FMT were treated with a second FMT. At last visit, eight of nine patients who completed all treatments were MDRO culture negative. FMT-treated participants had longer time to recurrent MDRO infection versus PREMIX-eligible controls who were not treated with FMT. Key taxa (Akkermansia muciniphila, Alistipes putredinis, Phocaeicola dorei, Phascolarctobacterium faecium, Alistipes species, Mesosutterella massiliensis, Barnesiella intestinihominis, and Faecalibacterium prausnitzii) from the single feces donor used in the study that engrafted in recipients and metabolites such as short-chain fatty acids and bile acids in FMT-responding participants uncovered leads for rational microbiome therapeutic and diagnostic development. Metagenomic analyses revealed a previously unobserved mechanism of MDRO eradication by conspecific strain competition in an FMT-treated subset. Susceptible Enterobacterales strains that replaced baseline extended-spectrum β-lactamase-producing strains were not detectable in donor microbiota manufactured as FMT doses but in one case were detectable in the recipient before FMT. These data suggest that FMT may provide a path to exploit strain competition to reduce MDRO colonization.
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