Pseudomonas aeruginosa extracellular products inhibit staphylococcal growth, and disrupt established biofilms produced by Staphylococcus epidermidis

Author:

Qin Zhiqiang123,Yang Liang3,Qu Di2,Molin Soeren3,Tolker-Nielsen Tim43

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, Hollings Cancer Center, Medical University of South Carolina, 86 Jonathan Lucas Street, Charleston, SC 29425, USA

2. Key Laboratory of Medical Molecular Virology of Ministry of Education and Public Health, Institutes of Biomedical Sciences and Institute of Medical Microbiology, Shanghai Medical School of Fudan University Box 228, Yi Xue Yuan Road 138#, Shanghai 200032, PR China

3. Centre for Biomedical Microbiology, BioCentrum-DTU, Technical University of Denmark, DK-2800 Lyngby, Denmark

4. Department of International Health, Immunology and Microbiology, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark

Abstract

Multiple bacterial species often coexist as communities, and compete for environmental resources. Here, we describe how an opportunistic pathogen,Pseudomonas aeruginosa, uses extracellular products to interact with the nosocomial pathogenStaphylococcus epidermidis.S. epidermidisbiofilms and planktonic cultures were challenged withP. aeruginosasupernatant cultures overnight. Results indicated that quorum-sensing-controlled factors fromP. aeruginosasupernatant inhibitedS. epidermidisgrowth in planktonic cultures. We also found thatP. aeruginosaextracellular products, mainly polysaccharides, disrupted establishedS. epidermidisbiofilms. Cellulase-treatedP. aeruginosasupernatant, and supernatant frompelA,pslFandpelApslBCDmutants, which are deficient in polysaccharide biosynthesis, diminished the disruption ofS. epidermidisbiofilms. In contrast,S. epidermidissupernatant in overnight cultures had no effect on establishedP. aeruginosabiofilms and planktonic growth. These findings reveal thatP. aeruginosaextracellular products are important microbial competition factors that overcome competition withS. epidermidis, and the results may provide clues for the development of a novel strategy for controllingS. epidermidisbiofilms.

Publisher

Microbiology Society

Subject

Microbiology

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