Small molecule signaling in regulation of gut microbiota structure and colonization resistance

The community of commensal microbes in the gut, the gut microbiota, participates in numerous processes key for human health, including protection against foreign microorganisms. A greater mechanistic understanding of how the gut microbiota resists the invasion of foreign bacteria, from pathogens to new commensal microorganisms, is essential both for the control of infection and in targeted approaches for microbiota manipulation. Our work has shown that interpersonal differences in the gut microbiota are an important driver of outcome of infection by Vibrio cholerae, the etiologic agent of cholera, a devastating diarrhea affecting millions of people each year worldwide. As a genetically tractable model organism for examining invasion of the gut microbial community, studies with V. cholerae allow for mechanistic examination of microbial colonization and inter-bacterial interaction and competition in the gastrointestinal tract. We have shown that small molecule signaling factors, including bacterial quorum sensing autoinducers, and microbial bile and diet metabolites, modulates microbiota structure and in turn multiple pathways of colonization resistance against V. cholerae. This proposal aims to define molecular mechanisms underpinning the ability of diverse human gut communities to drive the biochemical milieu of the gut into colonization-resistant or susceptible states, thus shaping resistance against colonization of both pathogens such as V. cholerae and new commensals. The proposed studies aim to provide mechanistic understanding for the processes driving assembly of gut microbial communities and identify new targets for prophylactic and therapeutic manipulations of the gut microbiota to combat invading microorganisms. Project Number: 1R35GM158026-01 | Fiscal Year: 2025 | NIH Institute/Center: National Institute of General Medical Sciences (NIGMS) | Principal Investigator: Ansel Hsiao | Institution: UNIVERSITY OF CALIFORNIA RIVERSIDE, RIVERSIDE, CA | Award Amount: $2,065,745 | Activity Code: R35 | Study Section: Maximizing Investigators' Research Award - F Study Section[MRAF] View on NIH RePORTER: https://reporter.nih.gov/project-details/11089182