Microbiota-activated PPAR-γ signaling inhibits dysbiotic Enterobacteriaceae expansion

Mariana X. Byndloss(University of California, Davis), Erin E. Olsan(University of California, Davis), Fabian Rivera-Chávez(University of California, Davis), Connor R. Tiffany(University of California, Davis), Stephanie A. Cevallos(University of California, Davis), Kristen L. Lokken(University of California, Davis), Teresa P. Torres(University of California, Davis), Austin J. Byndloss(University of California, Davis), Franziska Faber(University of California, Davis), Yandong Gao(University of California, Davis), Yael Litvak(University of California, Davis), Christopher A. Lopez(University of California, Davis), Gege Xu(University of California, Davis), Eleonora Napoli(University of California, Davis), Cecilia Giulivi(University of California, Davis), Renée M. Tsolis(University of California, Davis), Alexander Revzin(University of California, Davis), Carlito B. Lebrilla(University of California, Davis), Andreas J. Bäumler(University of California, Davis)
Science
August 11, 2017
Cited by 1,158

Abstract

Healthy guts exclude oxygen Normally, the lumen of the colon lacks oxygen. Fastidiously anaerobic butyrate-producing bacteria thrive in the colon; by ablating these organisms, antibiotic treatment removes butyrate. Byndloss et al. discovered that loss of butyrate deranges metabolic signaling in gut cells (see the Perspective by Cani). This induces nitric oxidase to generate nitrate in the lumen and disables β-oxidation in epithelial cells that would otherwise mop up stray oxygen before it enters the colon. Simultaneously, regulatory T cells retreat, and inflammation is unchecked, which contributes yet more oxygen species to the colon. Then, facultative aerobic pathogens, such as Escherichia coli and Salmonella enterica , can take advantage of the altered environment and outgrow any antibiotic-crippled and benign anaerobes. Science , this issue p. 570 ; see also p. 548


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