Pseudomonas aeruginosa biofilm exopolysaccharides: assembly, function, and degradation

Author:

Gheorghita Andreea A12ORCID,Wozniak Daniel J34,Parsek Matthew R5,Howell P Lynne12ORCID

Affiliation:

1. Program in Molecular Medicine, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children , 686 Bay St , Toronto, ON M5G 0A4, Canada

2. Department of Biochemistry, University of Toronto , Medical Science Building, 1 King's College Cir , Toronto, ON M5S 1A8, Canada

3. Department of Microbial Infection and Immunity, The Ohio State University College of Medicine , 776 Biomedical Research Tower, 460 W 12th Ave , Columbus, OH 43210, United States

4. Department of Microbiology, The Ohio State University College , Biological Sciences Bldg, 105, 484 W 12th Ave , Columbus, OH 43210, United States

5. Department of Microbiology, University of Washington , Health Sciences Bldg, 1705 NE Pacific St , Seattle, WA 98195-7735, United States

Abstract

Abstract The biofilm matrix is a fortress; sheltering bacteria in a protective and nourishing barrier that allows for growth and adaptation to various surroundings. A variety of different components are found within the matrix including water, lipids, proteins, extracellular DNA, RNA, membrane vesicles, phages, and exopolysaccharides. As part of its biofilm matrix, Pseudomonas aeruginosa is genetically capable of producing three chemically distinct exopolysaccharides – alginate, Pel, and Psl – each of which has a distinct role in biofilm formation and immune evasion during infection. The polymers are produced by highly conserved mechanisms of secretion, involving many proteins that span both the inner and outer bacterial membranes. Experimentally determined structures, predictive modelling of proteins whose structures are yet to be solved, and structural homology comparisons give us insight into the molecular mechanisms of these secretion systems, from polymer synthesis to modification and export. Here, we review recent advances that enhance our understanding of P. aeruginosa multiprotein exopolysaccharide biosynthetic complexes, and how the glycoside hydrolases/lyases within these systems have been commandeered for antimicrobial applications.

Funder

CIHR

NIH

Cystic Fibrosis Canada

Hospital for Sick Children

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology

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