Candida species differ in their interactions with immature human gastrointestinal epithelial cells

Pediatr Res. 2011 May;69(5 Pt 1):384-9. doi: 10.1203/PDR.0b013e31821269d5.

Abstract

Life-threatening gastrointestinal (GI) diseases of prematurity are highly associated with systemic candidiasis. This implicates the premature GI tract as an important site for invasion by Candida. Invasive interactions of Candida spp. with immature enterocytes have heretofore not been analyzed. Using a primary immature human enterocyte line, we compared the ability of multiple isolates of different Candida spp. to penetrate, injure, and induce a cytokine response from host cells. Of all the Candida spp. analyzed, C. albicans had the greatest ability to penetrate and injure immature enterocytes and to elicit IL-8 release (p < 0.01). In addition, C. albicans was the only Candida spp. to form filamentous hyphae when in contact with immature enterocytes. Similarly, a C. albicans mutant with defective hyphal morphogenesis and invasiveness had attenuated cytotoxicity for immature enterocytes (p < 0.003). Thus, hyphal morphogenesis correlates with immature enterocyte penetration, injury, and inflammatory responses. Furthermore, variability in enterocyte injury was observed among hyphal-producing C. albicans strains, suggesting that individual organism genotypes also influence host-pathogen interactions. Overall, the finding that Candida spp. differed in their interactions with immature enterocytes implicates that individual spp. may use different pathogenesis mechanisms.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Adhesion
  • Candida / classification
  • Candida / genetics
  • Candida / pathogenicity*
  • Cell Line
  • Enterocytes / immunology
  • Enterocytes / microbiology*
  • Enterocytes / pathology
  • Genotype
  • Host-Pathogen Interactions* / genetics
  • Humans
  • Hyphae
  • Inflammation Mediators / metabolism
  • Interleukin-8 / metabolism
  • Mutation
  • Phenotype

Substances

  • CXCL8 protein, human
  • Inflammation Mediators
  • Interleukin-8