Ren Xiaomei, Clark R Mason, Bansah Dziedzom A, Varner Elizabeth N, Tiffany Connor R, Jaswal Kanchan, Geary John H, Todd Olivia A, Winkelman Jonathan D, Friedman Elliot S, Zemel Babette S, Wu Gary D, Zackular Joseph P, DePas William H, Behnsen Judith, Palmer Lauren D
Department of Microbiology and Immunology, University of Illinois Chicago, Chicago, IL, USA.
Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
bioRxiv. 2024 Oct 19:2024.10.19.619093. doi: 10.1101/2024.10.19.619093.
Antimicrobial resistance is an urgent threat to human health. Asymptomatic colonization is often critical for persistence of antimicrobial-resistant pathogens. Gut colonization by the antimicrobial-resistant priority pathogen is associated with increased risk of clinical infection. Ecological factors shaping gut colonization remain unclear. Here we show that and other pathogenic evolved to utilize the amino acid ornithine, a non-preferred carbon source. utilizes ornithine to compete with the resident microbiota and persist in the gut in mice. Supplemental dietary ornithine promotes long-term fecal shedding of . By contrast, supplementation of a preferred carbon source-monosodium glutamate (MSG)-abolishes the requirement for ornithine catabolism. Additionally, we report evidence for diet promoting gut carriage in humans. Together, these results highlight that evolution of ornithine catabolism allows to compete with the microbiota in the gut, a reservoir for pathogen spread.
抗菌药物耐药性是对人类健康的紧迫威胁。无症状定植对于抗菌药物耐药病原体的持续存在往往至关重要。肠道被优先关注的抗菌药物耐药病原体定植与临床感染风险增加有关。影响肠道定植的生态因素仍不清楚。在这里,我们表明[病原体名称]和其他致病性病原体已进化为利用氨基酸鸟氨酸(一种非首选碳源)。[病原体名称]利用鸟氨酸与常驻微生物群竞争并在小鼠肠道中持续存在。补充膳食鸟氨酸可促进[病原体名称]的长期粪便排出。相比之下,补充首选碳源——味精(MSG)——消除了对[病原体名称]鸟氨酸分解代谢的需求。此外,我们报告了饮食促进人类肠道携带[病原体名称]的证据。总之,这些结果突出表明,鸟氨酸分解代谢的进化使[病原体名称]能够与肠道中的微生物群竞争,而肠道是病原体传播的一个储存库。