Siderophore-mediated zinc acquisition enhances enterobacterial colonization of the inflamed gut

Author:

Behnsen JudithORCID,Zhi Hui,Aron Allegra T.,Subramanian Vivekanandan,Santus WilliamORCID,Lee Michael H.,Gerner Romana R.,Petras DanielORCID,Liu Janet Z.ORCID,Green Keith D.,Price Sarah L.,Camacho Jose,Hillman Hannah,Tjokrosurjo Joshua,Montaldo Nicola P.,Hoover Evelyn M.,Treacy-Abarca Sean,Gilston Benjamin A.,Skaar Eric P.ORCID,Chazin Walter J.ORCID,Garneau-Tsodikova Sylvie,Lawrenz Matthew B.ORCID,Perry Robert D.,Nuccio Sean-Paul,Dorrestein Pieter C.ORCID,Raffatellu ManuelaORCID

Abstract

AbstractZinc is an essential cofactor for bacterial metabolism, and many Enterobacteriaceae express the zinc transporters ZnuABC and ZupT to acquire this metal in the host. However, the probiotic bacterium Escherichia coli Nissle 1917 (or “Nissle”) exhibits appreciable growth in zinc-limited media even when these transporters are deleted. Here, we show that Nissle utilizes the siderophore yersiniabactin as a zincophore, enabling Nissle to grow in zinc-limited media, to tolerate calprotectin-mediated zinc sequestration, and to thrive in the inflamed gut. We also show that yersiniabactin’s affinity for iron or zinc changes in a pH-dependent manner, with increased relative zinc binding as the pH increases. Thus, our results indicate that siderophore metal affinity can be influenced by the local environment and reveal a mechanism of zinc acquisition available to commensal and pathogenic Enterobacteriaceae.

Funder

U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases

U.S. Department of Health & Human Services | NIH | Center for Scientific Review

U.S. Department of Health & Human Services | National Institutes of Health

Crohn’s and Colitis Foundation

Gordon and Betty Moore Foundation

Burroughs Wellcome Fund

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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