Frontiers in Cellular and Infection Microbiology (May 2015)

Extracellular matrix-associated proteins form an integral and dynamic system during Pseudomonas aeruginosa biofilm development

  • Weipeng eZhang,
  • Jin eSun,
  • Wei eDing,
  • Jinshui eLin,
  • Renmao eTian,
  • Liang eLu,
  • Xiaofen eLiu,
  • Xihui eShen,
  • Pei-Yuan eQian

DOI
https://doi.org/10.3389/fcimb.2015.00040
Journal volume & issue
Vol. 5

Abstract

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Though the essential role of extracellular matrix in biofilm development has been extensively documented, the function of matrix-associated proteins is elusive. Determining the dynamics of matrix-associated proteins would be a useful way to reveal their functions in biofilm development. Therefore, we applied iTRAQ-based quantitative proteomics to evaluate matrix-associated proteins isolated from different phases of Pseudomonas aeruginosa ATCC27853 biofilms. Among the identified 389 proteins, 54 changed their abundance significantly. The increased abundance of stress resistance and nutrient metabolism-related proteins over the period of biofilm development was consistent with the hypothesis that biofilm matrix forms micro-environments in which cells are optimally organized to resist stress and use available nutrients. Secreted proteins, including novel putative effectors of the type III secretion system were identified, suggesting that the dynamics of pathogenesis-related proteins in the matrix are associated with biofilm development. Interestingly, there was a good correlation between the abundance changes of matrix-associated proteins and their expression. Further analysis revealed complex interactions among these modulated proteins, and the mutation of selected proteins attenuated biofilm development. Collectively, this work presents the first dynamic picture of matrix-associated proteins during biofilm development, and provides evidences that the matrix-associated proteins may form an integral and well regulated system that contributes to stress resistance, nutrient acquisition, pathogenesis and the stability of the biofilm.

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