Mannose-binding lectin deficiency facilitates abdominal Candida infections in patients with secondary peritonitis

Clin Vaccine Immunol. 2008 Jan;15(1):65-70. doi: 10.1128/CVI.00297-07. Epub 2007 Oct 31.

Abstract

Mannose-binding lectin (MBL) deficiency due to variations in the MBL gene is associated with increased susceptibility to infections. In this study, the association between MBL deficiency and the occurrence of abdominal yeast infection (AYI) in peritonitis patients was examined. Eighty-eight patients with secondary peritonitis requiring emergency laparotomy were included. MBL genotype (wild type [WT] versus patients with variant genotypes), MBL plasma concentrations, and Candida risk factors were examined in patients with and those without AYI (positive abdominal yeast cultures during [re]laparotomy). A variant MBL genotype was found in 53% of patients with AYI and 38% of those without AYI (P = 0.18). A significantly higher proportion of variant patients had an AYI during early peritonitis (during first laparotomy) than WT patients (39% versus 16%, respectively; P = 0.012). Patients with AYI had lower MBL levels than did patients without AYI (0.16 microg/ml [0.0 to 0.65 microg/ml] versus 0.65 microg/ml (0.19 to 1.95 microg/ml); P = 0.007). Intensity of colonization (odds ratio [OR], 1.1; 95% confidence interval [CI], 1.0 to 1.1), MBL plasma concentrations of <0.5 microg/ml (OR, 4.5; 95% CI, 1.2 to 16.3), and numbers of relaparotomies (OR, 1.7; 95% CI, 1.0 to 2.8) were independently associated with AYI. In summary, deficient MBL plasma levels were independently associated with the development of AYI in patients with secondary peritonitis and seemed to facilitate early infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alleles
  • Candida / isolation & purification*
  • Candidiasis / genetics
  • Candidiasis / metabolism*
  • Candidiasis / microbiology
  • Cohort Studies
  • Fungemia / genetics
  • Fungemia / metabolism
  • Fungemia / microbiology
  • Genetic Predisposition to Disease
  • Humans
  • Mannose-Binding Lectins / blood
  • Mannose-Binding Lectins / deficiency*
  • Mannose-Binding Lectins / genetics
  • Middle Aged
  • Peritonitis / genetics
  • Peritonitis / metabolism*
  • Peritonitis / microbiology
  • Polymorphism, Genetic
  • Prospective Studies

Substances

  • Mannose-Binding Lectins