» Articles » PMID: 32885535

Interbacterial Competition and Anti-predatory Behaviour of Environmental Vibrio Cholerae Strains

Overview
Date 2020 Sep 5
PMID 32885535
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Vibrio cholerae isolates responsible for cholera pandemics represent only a small portion of the diverse strains belonging to this species. Indeed, most V. cholerae are encountered in aquatic environments. To better understand the emergence of pandemic lineages, it is crucial to discern what differentiates pandemic strains from their environmental relatives. Here, we studied the interaction of environmental V. cholerae with eukaryotic predators or competing bacteria and tested the contributions of the haemolysin and the type VI secretion system (T6SS) to those interactions. Both of these molecular weapons are constitutively active in environmental isolates but subject to tight regulation in the pandemic clade. We showed that several environmental isolates resist amoebal grazing and that this anti-grazing defense relies on the strains' T6SS and its actincross-linking domain (ACD)-containing tip protein. Strains lacking the ACD were unable to defend themselves against grazing amoebae but maintained high levels of T6SS-dependent interbacterial killing. We explored the latter phenotype through whole-genome sequencing of 14 isolates, which unveiled a wide array of novel T6SS effector and (orphan) immunity proteins. By combining these in silico predictions with experimental validations, we showed that highly similar but non-identical immunity proteins were insufficient to provide cross-immunity among those wild strains.

Citing Articles

Multiplicity of type 6 secretion system toxins limits the evolution of resistance.

Smith W, Armstrong-Bond E, Coyte K, Knight C, Basler M, Brockhurst M Proc Natl Acad Sci U S A. 2025; 122(2):e2416700122.

PMID: 39786933 PMC: 11745330. DOI: 10.1073/pnas.2416700122.


The coral pathogen Vibrio coralliilyticus uses a T6SS to secrete a group of novel anti-eukaryotic effectors that contribute to virulence.

Mass S, Cohen H, Podicheti R, Rusch D, Gerlic M, Ushijima B PLoS Biol. 2024; 22(9):e3002734.

PMID: 39226241 PMC: 11371242. DOI: 10.1371/journal.pbio.3002734.


Mechanisms of bacterial immunity, protection, and survival during interbacterial warfare.

Kennedy N, Comstock L Cell Host Microbe. 2024; 32(6):794-803.

PMID: 38870897 PMC: 11216714. DOI: 10.1016/j.chom.2024.05.006.


Genome sequences of strains isolated in the DRC between 2009 and 2012.

Lemopoulos A, Miwanda B, Drebes Dorr N, Stutzmann S, Bompangue D, Muyembe-Tamfum J Microbiol Resour Announc. 2024; 13(3):e0082723.

PMID: 38345380 PMC: 10927689. DOI: 10.1128/mra.00827-23.


The RIX domain defines a class of polymorphic T6SS effectors and secreted adaptors.

Kanarek K, Fridman C, Bosis E, Salomon D Nat Commun. 2023; 14(1):4983.

PMID: 37591831 PMC: 10435454. DOI: 10.1038/s41467-023-40659-2.


References
1.
Unterweger D, Miyata S, Bachmann V, Brooks T, Mullins T, Kostiuk B . The Vibrio cholerae type VI secretion system employs diverse effector modules for intraspecific competition. Nat Commun. 2014; 5:3549. PMC: 3988814. DOI: 10.1038/ncomms4549. View

2.
Benghezal M, Fauvarque M, Tournebize R, Froquet R, Marchetti A, Bergeret E . Specific host genes required for the killing of Klebsiella bacteria by phagocytes. Cell Microbiol. 2005; 8(1):139-48. DOI: 10.1111/j.1462-5822.2005.00607.x. View

3.
Buist G, Steen A, Kok J, Kuipers O . LysM, a widely distributed protein motif for binding to (peptido)glycans. Mol Microbiol. 2008; 68(4):838-47. DOI: 10.1111/j.1365-2958.2008.06211.x. View

4.
Logan S, Thomas J, Yan J, Baker R, Shields D, Xavier J . The type VI secretion system can modulate host intestinal mechanics to displace gut bacterial symbionts. Proc Natl Acad Sci U S A. 2018; 115(16):E3779-E3787. PMC: 5910850. DOI: 10.1073/pnas.1720133115. View

5.
Wattam A, Davis J, Assaf R, Boisvert S, Brettin T, Bun C . Improvements to PATRIC, the all-bacterial Bioinformatics Database and Analysis Resource Center. Nucleic Acids Res. 2016; 45(D1):D535-D542. PMC: 5210524. DOI: 10.1093/nar/gkw1017. View