Department of Pathology and Rogel Cancer Center, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Department of Pathology and Rogel Cancer Center, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Cell Host Microbe. 2020 Oct 7;28(4):526-533.e5. doi: 10.1016/j.chom.2020.06.018. Epub 2020 Jul 28.
The microbiota confers host protection by limiting the colonization of pathogenic bacteria in the gut, but the mechanisms by which pathogens overcome colonization resistance remain poorly understood. Using a high-density transposon screen in the enteric pathogen Citrobacter rodentium, we find that the bacterium requires amino acid biosynthesis pathways to colonize conventionally raised mice, but not germ-free or antibiotic-treated animals. These metabolic pathways are induced during infection by the presence of the gut microbiota. Reduced amounts of amino acids are found in the guts of conventionally raised mice compared with germ-free animals. Dietary administration of high protein increases amino acid levels in the gut and promotes pathogen colonization. Thus, the depletion of amino acids by the microbiota limits pathogen colonization, and in turn, the pathogen activates amino acid biosynthesis to expand in the presence of the microbiota.
微生物群通过限制肠道中致病菌的定植来赋予宿主保护,但宿主对定植抵抗的机制仍知之甚少。在肠道病原体柠檬酸杆菌中使用高密度转座子筛选,我们发现细菌需要氨基酸生物合成途径来定植常规饲养的小鼠,但不能定植无菌或用抗生素处理的动物。这些代谢途径在肠道微生物群存在的情况下被诱导。与无菌动物相比,常规饲养的小鼠肠道中的氨基酸含量减少。膳食中高蛋白的添加增加了肠道中的氨基酸水平,并促进了病原体的定植。因此,微生物群消耗氨基酸会限制病原体的定植,而反过来,病原体激活氨基酸生物合成以在微生物群存在的情况下扩张。