A Vibrio cholerae protease needed for killing of Caenorhabditis elegans has a role in protection from natural predator grazing

Proc Natl Acad Sci U S A. 2006 Jun 13;103(24):9280-5. doi: 10.1073/pnas.0601754103. Epub 2006 Jun 5.

Abstract

Vibrio cholerae is the causal bacterium of the diarrheal disease cholera, and its growth and survival are thought to be curtailed by bacteriovorous predators, e.g., ciliates and flagellates. We explored Caenorhabditis elegans as a test organism after finding that V. cholerae can cause lethal infection of this nematode. By reverse genetics we identified an extracellular protease, the previously uncharacterized PrtV protein, as being necessary for killing. The killing effect is associated with the colonization of bacteria within the Caenorhabditis elegans intestine. We also show that PrtV is essential for V. cholerae in the bacterial survival from grazing by the flagellate Cafeteria roenbergensis and the ciliate Tetrahymena pyriformis. The PrtV protein appears to have an indirect role in the interaction of V. cholerae with mammalian host cells as judged from tests with tight monolayers of human intestinal epithelial cells. Our results demonstrate a key role for PrtV in V. cholerae interaction with grazing predators, and we establish Caenorhabditis elegans as a convenient organism for identification of V. cholerae factors involved in host interactions and environmental persistence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Biofilms
  • Caenorhabditis elegans / cytology
  • Caenorhabditis elegans / microbiology*
  • Caenorhabditis elegans / physiology*
  • Cell Communication
  • Cell Line, Tumor
  • Cholera Toxin / metabolism
  • Feeding Behavior
  • Fimbriae, Bacterial / metabolism
  • Humans
  • Interleukin-8 / metabolism
  • Intestines / cytology
  • Intestines / microbiology
  • Peptide Hydrolases / genetics
  • Peptide Hydrolases / metabolism*
  • Predatory Behavior*
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Survival Rate
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Vibrio cholerae / enzymology*
  • Vibrio cholerae / genetics
  • Vibrio cholerae / pathogenicity*

Substances

  • Bacterial Proteins
  • Interleukin-8
  • LuxO protein, Vibrio harveyi
  • Repressor Proteins
  • Trans-Activators
  • Transcription Factors
  • LuxR autoinducer binding proteins
  • Cholera Toxin
  • Peptide Hydrolases
  • PrtV protein, Vibrio cholerae