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Cysteine dependence of Lactobacillus iners is a potential therapeutic target for vaginal microbiota modulation

生物 脆乳杆菌 细菌性阴道病 基因组 乳酸菌 微生物学 失调 微生物群 遗传学 细菌 基因
作者
Seth M. Bloom,Nomfuneko A. Mafunda,Benjamin M. Woolston,Matthew R. Hayward,Josephine F. Frempong,Aaron B. Abai,Jiawu Xu,Alissa J. Mitchell,Xavier Westergaard,Fatima A. Hussain,Nondumiso Xulu,Mary Dong,Krista L. Dong,Thandeka Gumbi,Fransisca Xolisile Ceasar,Justin K. Rice,Namit Choksi,Nasreen Ismail,Thumbi Ndung’u,Musie Ghebremichael,David A. Relman,Emily P. Balskus,Caroline M. Mitchell,Douglas S. Kwon
出处
期刊:Nature microbiology [Nature Portfolio]
卷期号:7 (3): 434-450 被引量:60
标识
DOI:10.1038/s41564-022-01070-7
摘要

Vaginal microbiota composition affects many facets of reproductive health. Lactobacillus iners-dominated microbial communities are associated with poorer outcomes, including higher risk of bacterial vaginosis (BV), compared with vaginal microbiota rich in L. crispatus. Unfortunately, standard-of-care metronidazole therapy for BV typically results in dominance of L. iners, probably contributing to post-treatment relapse. Here we generate an L. iners isolate collection comprising 34 previously unreported isolates from 14 South African women with and without BV and 4 previously unreported isolates from 3 US women. We also report an associated genome catalogue comprising 1,218 vaginal Lactobacillus isolate genomes and metagenome-assembled genomes from >300 women across 4 continents. We show that, unlike L. crispatus, L. iners growth is dependent on l-cysteine in vitro and we trace this phenotype to the absence of canonical cysteine biosynthesis pathways and a restricted repertoire of cysteine-related transport mechanisms. We further show that cysteine concentrations in cervicovaginal lavage samples correlate with Lactobacillus abundance in vivo and that cystine uptake inhibitors selectively inhibit L. iners growth in vitro. Combining an inhibitor with metronidazole promotes L. crispatus dominance of defined BV-like communities in vitro by suppressing L. iners growth. Our findings enable a better understanding of L. iners biology and suggest candidate treatments to modulate the vaginal microbiota to improve reproductive health for women globally. l-cysteine is required for the growth of Lactobacillus iners, a vaginal microbiome species typically associated with adverse outcomes that lacks cysteine biosynthesis pathways and key uptake mechanisms present in other lactobacilli. Cystine uptake inhibitors can be used to suppress L. iners abundance in vitro in favour of L. crispatus, a species associated with favourable outcomes.
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