» Articles » PMID: 23828520

Killing of Escherichia Coli by Myxococcus Xanthus in Aqueous Environments Requires Exopolysaccharide-dependent Physical Contact

Overview
Journal Microb Ecol
Date 2013 Jul 6
PMID 23828520
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Nutrient or niche-based competition among bacteria is a widespread phenomenon in the natural environment. Such interspecies interactions are often mediated by secreted soluble factors and/or direct cell-cell contact. As ubiquitous soil bacteria, Myxococcus species are able to produce a variety of bioactive secondary metabolites to inhibit the growth of other competing bacterial species. Meanwhile, Myxococcus spp. also exhibit sophisticated predatory behavior, an extreme form of competition that is often stimulated by close contact with prey cells and largely depends on the availability of solid surfaces. Myxococcus spp. can also be isolated from aquatic environments. However, studies focusing on the interaction between Myxococcus and other bacteria in such environments are still limited. In this study, using the well-studied Myxococcus xanthus DK1622 and Escherichia coli as model interspecies interaction pair, we demonstrated that in an aqueous environment, M. xanthus was able to kill E. coli in a cell contact-dependent manner and that the observed contact-dependent killing required the formation of co-aggregates between M. xanthus and E. coli cells. Further analysis revealed that exopolysaccharide (EPS), type IV pilus, and lipopolysaccharide mutants of M. xanthus displayed various degrees of attenuation in E. coli killing, and it correlated well with the mutants' reduction in EPS production. In addition, M. xanthus showed differential binding ability to different bacteria, and bacterial strains unable to co-aggregate with M. xanthus can escape the killing, suggesting the specific nature of co-aggregation and the targeted killing of interacting bacteria. In conclusion, our results demonstrated EPS-mediated, contact-dependent killing of E. coli by M. xanthus, a strategy that might facilitate the survival of this ubiquitous bacterium in aquatic environments.

Citing Articles

Integrated assessment of mucilage impact on human health using the One Health approach: Prevalence and antimicrobial resistance profiles of and in the Marmara Sea, Türkiye.

Yibar A, Ay H, Aydin F, Abay S, Karakaya E, Kayman T Heliyon. 2025; 11(3):e42103.

PMID: 39916849 PMC: 11800074. DOI: 10.1016/j.heliyon.2025.e42103.


Comparative genomics and transcriptomics insight into myxobacterial metabolism potentials and multiple predatory strategies.

Wang C, Xiao Y, Wang Y, Liu Y, Yao Q, Zhu H Front Microbiol. 2023; 14:1146523.

PMID: 37213496 PMC: 10196010. DOI: 10.3389/fmicb.2023.1146523.


Myxobacterial Predation: A Standardised Lawn Predation Assay Highlights Strains with Unusually Efficient Predatory Activity.

Zwarycz A, Whitworth D Microorganisms. 2023; 11(2).

PMID: 36838363 PMC: 9967850. DOI: 10.3390/microorganisms11020398.


Concepts and conjectures concerning predatory performance of myxobacteria.

Phillips K, Akbar S, Stevens D Front Microbiol. 2022; 13:1031346.

PMID: 36246230 PMC: 9556981. DOI: 10.3389/fmicb.2022.1031346.


Adaptive Evolution of Geobacter sulfurreducens in Coculture with Pseudomonas aeruginosa.

Semenec L, Vergara I, Laloo A, Petrovski S, Bond P, Franks A mBio. 2020; 11(2).

PMID: 32265334 PMC: 7157779. DOI: 10.1128/mBio.02875-19.


References
1.
Campos J, GEISSELSODER J, Zusman D . Isolation of bacteriophage MX4, a generalized transducing phage for Myxococcus xanthus. J Mol Biol. 1978; 119(2):167-78. DOI: 10.1016/0022-2836(78)90431-x. View

2.
He X, Tian Y, Guo L, Lux R, Zusman D, Shi W . Oral-derived bacterial flora defends its domain by recognizing and killing intruders--a molecular analysis using Escherichia coli as a model intestinal bacterium. Microb Ecol. 2010; 60(3):655-64. PMC: 2954290. DOI: 10.1007/s00248-010-9708-4. View

3.
Spormann A . Gliding motility in bacteria: insights from studies of Myxococcus xanthus. Microbiol Mol Biol Rev. 1999; 63(3):621-41. PMC: 103748. DOI: 10.1128/MMBR.63.3.621-641.1999. View

4.
Reichenbach H . The ecology of the myxobacteria. Environ Microbiol. 2001; 1(1):15-21. DOI: 10.1046/j.1462-2920.1999.00016.x. View

5.
Bowden M, Kaplan H . The Myxococcus xanthus lipopolysaccharide O-antigen is required for social motility and multicellular development. Mol Microbiol. 1998; 30(2):275-84. DOI: 10.1046/j.1365-2958.1998.01060.x. View