Gene and protein expression in response to different growth temperatures and oxygen availability in Burkholderia thailandensis

PLoS One. 2014 Mar 26;9(3):e93009. doi: 10.1371/journal.pone.0093009. eCollection 2014.

Abstract

Burkholderia thailandensis, although normally avirulent for mammals, can infect macrophages in vitro and has occasionally been reported to cause pneumonia in humans. It is therefore used as a model organism for the human pathogen B. pseudomallei, to which it is closely related phylogenetically. We characterized the B. thailandensis clinical isolate CDC2721121 (BtCDC272) at the genome level and studied its response to environmental cues associated with human host colonization, namely, temperature and oxygen limitation. Effects of the different growth conditions on BtCDC272 were studied through whole genome transcription studies and analysis of proteins associated with the bacterial cell surface. We found that growth at 37°C, compared to 28°C, negatively affected cell motility and flagella production through a mechanism involving regulation of the flagellin-encoding fliC gene at the mRNA stability level. Growth in oxygen-limiting conditions, in contrast, stimulated various processes linked to virulence, such as lipopolysaccharide production and expression of genes encoding protein secretion systems. Consistent with these observations, BtCDC272 grown in oxygen limitation was more resistant to phagocytosis and strongly induced the production of inflammatory cytokines from murine macrophages. Our results suggest that, while temperature sensing is important for regulation of B. thailandensis cell motility, oxygen limitation has a deeper impact on its physiology and constitutes a crucial environmental signal for the production of virulence factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Biopolymers / metabolism
  • Burkholderia / drug effects
  • Burkholderia / genetics*
  • Burkholderia / growth & development*
  • Burkholderia / ultrastructure
  • Cell Communication / drug effects
  • Cell Movement / drug effects
  • Gene Expression Regulation, Bacterial / drug effects
  • Genome, Bacterial
  • Lipopolysaccharides / metabolism
  • Mice
  • Myeloid Cells / metabolism
  • Neutrophils / drug effects
  • Neutrophils / metabolism
  • Oxygen / pharmacology*
  • Paraffin Embedding
  • Phagocytosis / drug effects
  • Polyhydroxyalkanoates / pharmacology
  • RAW 264.7 Cells
  • Real-Time Polymerase Chain Reaction
  • Reproducibility of Results
  • Sequence Analysis, DNA
  • Sequence Analysis, RNA
  • Temperature*
  • Time Factors

Substances

  • Bacterial Proteins
  • Biopolymers
  • Lipopolysaccharides
  • Polyhydroxyalkanoates
  • Oxygen

Grants and funding

This work was supported by Fondazione CARIPLO (Progetto Vaccini, contract number 2009–3577) and by Ministero dell’Istruzione, dell’Università e della Ricerca (MIUR) (project FIRB RBLA039LSF). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.