Gallocin A, an Atypical Two-Peptide Bacteriocin with Intramolecular Disulfide Bonds Required for Activity

Author:

Proutière Alexis1,du Merle Laurence1,Garcia-Lopez Marta1,Léger Corentin2,Voegele Alexis2,Chenal Alexandre2,Harrington Antony3,Tal-Gan Yftah3ORCID,Cokelaer Thomas45,Trieu-Cuot Patrick1,Dramsi Shaynoor1ORCID

Affiliation:

1. Institut Pasteur, Université Paris Cité, CNRS UMR6047, Biology of Gram-Positive Pathogens Unit, Paris, France

2. Institut Pasteur, Université Paris Cité, CNRS UMR3528, Biochemistry of Macromolecular Interactions Unit, Paris, France

3. Department of Chemistry, University of Nevada, Reno, Reno Nevada, USA

4. Institut Pasteur, Université Paris Cité, Plateforme Technologique Biomics, Paris, France

5. Institut Pasteur, Université Paris Cité, Bioinformatics and Biostatistics Hub, Paris, France

Abstract

Streptococcus gallolyticus subsp. gallolyticus ( SGG ), previously named Streptococcus bovis biotype I, is an opportunistic pathogen responsible for invasive infections (septicemia, endocarditis) in elderly people and is often associated with colon tumors. SGG is one of the first bacteria to be associated with the occurrence of colorectal cancer in humans. Previously, we showed that tumor-associated conditions in the colon provide SGG with an ideal environment to proliferate at the expense of phylogenetically and metabolically closely related commensal bacteria such as enterococci (1). SGG takes advantage of CRC-associated conditions to outcompete and substitute commensal members of the gut microbiota using a specific bacteriocin named gallocin, recently renamed gallocin A following the discovery of gallocin D in a peculiar SGG isolate.

Funder

Institut National Du Cancer

Agence Nationale de la Recherche

National Science Foundation

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Cell Biology,Microbiology (medical),Genetics,General Immunology and Microbiology,Ecology,Physiology

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