Infant acquisition of Stickland-metabolizing bacteria prevents Clostridium botulinum infection
Nobuhide KobayashiiD, Yotaro KodairaiD, Jiayue YangiD, Takuhiro MatsumuraiD, Aki Yamaguchi, Yuta AraiiD, Daisuke TakahashiiD, Hiroki Toriumi, Seiga KomiyamaiD, Kanon Iwata, Natsuki Haga, Yukina Nishida, Kazuki SaitoiD, Daisuke MotookaiD, Yuki MatsumotoiD, Shota NakamuraiD, Taizo WadaiD, Shinji FukudaiD, Koji HaseiD, Yukako FujinagaiD
Abstract
Infant botulism is caused by intestinal colonization with Clostridium botulinum, whereas healthy adults are resistant. Although the gut microbiota has long been implicated in protection against C. botulinum, its bacterial basis has remained unknown. Here, we show that specific amino acid-metabolizing bacteria confer resistance to C. botulinum colonization through nutrient competition. Longitudinally collected human infant microbiotas exhibited a transition from susceptibility to resistance after transplantation into germ-free mice. 5-Aminovalerate marked the resistant microbiota, implicating Stickland metabolism. Resistant microbiotas were enriched in Stickland-metabolizing Clostridia, including Clostridioides difficile. Metabolomics revealed overlapping amino acid utilization, and C. difficile suppressed C. botulinum expansion through amino acid competition. These findings demonstrate that acquisition of Stickland-metabolizing Clostridia during infancy prevents C. botulinum infection through competition for shared amino-acid-dependent nutritional niches.
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