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Apolipoprotein-E-deficient mice exhibit an increased susceptibility to disseminated candidiasis

Med Mycol. 2004 Aug;42(4):341-8. doi: 10.1080/13693780410001657135.

Abstract

The effect of hyperlipoproteinemia on systemic candidiasis was investigated by assessing the susceptibility of hyperlipoproteinemic, apolipoprotein E (ApoE)-deficient (ApoE -/-) mice to a systemic Candida albicans infection. The absence of ApoE in these mice resulted in an eightfold increase in plasma lipoprotein concentrations in the very low-density lipoprotein (VLDL) fraction, as compared with levels seen in ApoE +/+ mice. Mortality due to candidemia was significantly higher (86%) in ApoE -/- mice than in ApoE+/+ mice (52%), and in platings of homogenized kidney material on fungal culture medium, ApoE -/- mice yielded significantly higher levels of C. albicans outgrowth than did ApoE+/+ mice. C albicans grew twofold better in ApoE -/- plasma in 4 h than in ApoE+/+ plasma, and depletion of lipoproteins from plasma resulted in a significant seven- to tenfold increase in C. albicans growth. Recombinant ApoE did not directly inhibit C. albicans growth. Our data indicate that the increased susceptibility of ApoE -/- mice to C albicans is due both to increased growth of blastoconidia in ApoE -/- mice in response to the availability of lipids as nutrients, and to the neutralization of candidacidal factors by lipoproteins. This study suggests that lipoproteins play a significant role in host defense against candidiasis.

MeSH terms

  • Animals
  • Apolipoproteins E / blood
  • Apolipoproteins E / deficiency
  • Apolipoproteins E / genetics
  • Apolipoproteins E / physiology*
  • Candida albicans / growth & development
  • Candida albicans / pathogenicity*
  • Candidiasis / genetics*
  • Candidiasis / microbiology
  • Candidiasis / mortality
  • Candidiasis / physiopathology*
  • Fungemia / microbiology
  • Fungemia / mortality
  • Genetic Predisposition to Disease*
  • Hyperlipoproteinemias / complications
  • Lipoproteins, VLDL / metabolism
  • Mice
  • Mice, Inbred C57BL

Substances

  • Apolipoproteins E
  • Lipoproteins, VLDL