Host stress and virulence expression in intestinal pathogens: Development of therapeutic strategies using mice and C. elegans

Olga Zaborina, Alexander Zaborin, Kathleen Romanowski, Trissa Babrowski, John Alverdy

Research output: Contribution to journalReview article

19 Scopus citations

Abstract

The intestinal tract of a host exposed to extreme physiologic stress and modern medical intervention represents a relatively unexplored yet important area of infection research, given the frequency with which this site becomes colonized by highly pathogenic microorganisms that cause subsequent sepsis. Our laboratory has focused on the host tissue derived environmental cues that are released into the intestinal tract during extreme physiologic stress that induce the expression of virulence in colonizing pathogens with the goal of developing novel gut directed therapies that maintain host pathogen neutrality through the course of host stress. Here we demonstrate that maintenance of phosphate sufficiency/ abundance within the intestinal microenvironment may be considered as a universal strategy to prevent virulence activation across a broad range of pathogens that colonize the gut and cause sepsis, given that phosphate depletion occurs following stress and is a universal cue that activates the virulence of a wide variety of organisms. Using small animal models (Caenorhabditis elegans and mice) to create local phosphate depletion at sites of colonization of Pseudomonas aeruginosa, a common cause of lethal gut-derived sepsis, we demonstrate the importance of maintaining phosphate sufficiency to suppress the expression of a lethal phenotype during extreme physiologic stress. The molecular details and potential therapeutic implications are reviewed.

Original languageEnglish (US)
Pages (from-to)1254-1260
Number of pages7
JournalCurrent Pharmaceutical Design
Volume17
Issue number13
DOIs
StatePublished - Jan 1 2011
Externally publishedYes

Keywords

  • Gut-derived sepsis
  • Mouse model of physiologically stressed host
  • Phosphate limitation
  • Pseudomonas aeruginosa

ASJC Scopus subject areas

  • Pharmacology
  • Drug Discovery

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