<i>Salmonella</i> produces sulfide to compete with <i>Escherichia coli</i> in the gut lumen

A Anaïs B. Larabi (Department of Medical Microbiology and Immunology, School of Medicine, University of California) C Connor R. Tiffany (Department of Medical Microbiology and Immunology, School of Medicine, University of California) H Hugo L. P. Masson (Department of Medical Microbiology and Immunology, School of Medicine, University of California) H Henry Nguyen (Department of Medical Microbiology and Immunology, School of Medicine, University of California) E Eli J. Bejarano (Department of Medical Microbiology and Immunology, School of Medicine, University of California) M Megan J. Liou (Department of Medical Microbiology and Immunology, School of Medicine, University of California) L Lauren C. Radlinski (Department of Medical Microbiology and Immunology, School of Medicine, University of California) A Aurore M. Demars (Department of Medical Microbiology and Immunology, School of Medicine, University of California) R Renée M. Tsolis (Department of Medical Microbiology and Immunology, School of Medicine, University of California) A Andreas J. Bäumler (Department of Medical Microbiology and Immunology, School of Medicine, University of California)

Abstract

Hydrogen sulfide production is a characteristic that distinguishes Salmonella serovars from closely related species, such as Escherichia coli , but its biological significance remains obscure. Here, we show that PhsABC and AsrABC-mediated hydrogen sulfide production by Salmonella enterica serovar ( S. ) Typhimurium was linked to an increased abundance of Deltaproteobacteria and inhibition of cytochrome bd oxidase-mediated aerobic respiration of Escherichia coli in the murine large intestine. Functional phsABC and asrABC operons provided a growth benefit to S. Typhimurium in the cecum of Enterobacterales- free conventional mice only upon inoculation with commensal E. coli. In gnotobiotic mice engrafted with a defined community of 17 human Clostridia isolates, S. Typhimurium infection inhibited cytochrome bd oxidase-mediated aerobic respiration in E. coli only in the presence of Desulfovibrio piger , a sulfide-producing representative of the Deltaproteobacteria. A S. Typhimurium strain deficient for hydrogen sulfide production ( phsA asrA mutant) did not inhibit cytochrome bd oxidase-mediated aerobic respiration in E. coli , even when D. piger was present. Collectively, these data suggest that the phsABC and asrABC operons of Salmonella serovars provide a benefit during competition with closely related bacteria, such as E. coli , by inhibiting cytochrome bd oxidase-mediated aerobic respiration of the commensal.

Article Details

Volume / Issue Vol. 122, Issue 37
Published September 16, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (10)

A

Anaïs B. Larabi

Department of Medical Microbiology and Immunology, School of Medicine, University of California

C

Connor R. Tiffany

Department of Medical Microbiology and Immunology, School of Medicine, University of California

H

Hugo L. P. Masson

Department of Medical Microbiology and Immunology, School of Medicine, University of California

H

Henry Nguyen

Department of Medical Microbiology and Immunology, School of Medicine, University of California

E

Eli J. Bejarano

Department of Medical Microbiology and Immunology, School of Medicine, University of California

M

Megan J. Liou

Department of Medical Microbiology and Immunology, School of Medicine, University of California

L

Lauren C. Radlinski

Department of Medical Microbiology and Immunology, School of Medicine, University of California

A

Aurore M. Demars

Department of Medical Microbiology and Immunology, School of Medicine, University of California

R

Renée M. Tsolis

Department of Medical Microbiology and Immunology, School of Medicine, University of California

A

Andreas J. Bäumler

Department of Medical Microbiology and Immunology, School of Medicine, University of California