Proteomic studies highlight outer‐membrane proteins related to biofilm development in the marine bacterium Pseudoalteromonas sp. D41

peer-reviewed · PROTEOMICS · 2012

peer-reviewed · PROTEOMICS · 2012. Andrés Ritter et al. Bacterial biofilm development is conditioned by complex processes involving bacterial attachment to surfaces…
Date 2012-11-01
Type peer-reviewed
Venue PROTEOMICS
Publisher Wiley
Contribution downstream-application
DOI 10.1002/pmic.201100644
Citations (OpenAlex) 41

Abstract

Bacterial biofilm development is conditioned by complex processes involving bacterial attachment to surfaces, growth, mobility, and exoproduct production. The marine bacterium Pseudoalteromonas sp. strain D41 is able to attach strongly onto a wide variety of substrates, which promotes subsequent biofilm development. Study of the outer-membrane and total soluble proteomes showed ten spots with significant intensity variations when this bacterium was grown in biofilm compared to planktonic cultures. MS/MS de novo sequencing analysis allowed the identification of four outer-membrane proteins of particular interest since they were strongly induced in biofilms. These proteins are homologous to a TonB-dependent receptor (TBDR), to the OmpW and OmpA porins, and to a type IV pilus biogenesis protein (PilF). Gene expression assays by quantitative RT-PCR showed that the four corresponding genes were upregulated during biofilm development on hydrophobic and hydrophilic surfaces. The Pseudomonas aeruginosa mutants unable to produce any of the OmpW, OmpA, and PilF homologues yielded biofilms with lower biovolumes and altered architectures, confirming the involvement of these proteins in the biofilm formation process. Our results indicate that Pseudoalteromonas sp. D41 shares biofilm formation mechanisms with human pathogenic bacteria, but also relies on TBDR, which might be more specific to the marine environment.

Authors

  1. Andrés Ritter · Ifremer, Laboratoire de Biotechnologie et Chimie Marines, Université de Bretagne Sud
  2. Emmanuelle Com · Inserm, Institut de Recherche en Santé, Environnement et Travail
  3. Alexis Bazire · Laboratoire de Biotechnologie et Chimie Marines, Université de Bretagne Sud
  4. Marina Dos Santos Goncalves · Laboratoire de Biotechnologie et Chimie Marines, Université de Bretagne Sud
  5. Ludovic Delage · Centre National de la Recherche Scientifique, Station Biologique de Roscoff, Université Pierre-et-Marie-Curie
  6. Gaël Le Pennec · Laboratoire de Biotechnologie et Chimie Marines, Université de Bretagne Sud
  7. Charles Pineau · Inserm, Institut de Recherche en Santé, Environnement et Travail
  8. Catherine Dreanno · Ifremer
  9. Chantal Compère · Ifremer
  10. Alain Dufour · Laboratoire de Biotechnologie et Chimie Marines, Université de Bretagne Sud

Methods and tools

Methods it uses

  • PEAKS: Commercial DP-based de novo

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