A Polymorphism in the Chitotriosidase Gene Associated with Risk of Mycetoma Due to Madurella mycetomatis Mycetoma--A Retrospective Study

PLoS Negl Trop Dis. 2015 Sep 2;9(9):e0004061. doi: 10.1371/journal.pntd.0004061. eCollection 2015.

Abstract

Background: Madurella mycetomatis is the most prevalent causative agent of eumycetoma in Sudan, an infection characterized by the formation of grains. Many patients are exposed to the causative agent, however only a small number develop infection. M. mycetomatis contains chitin in its cell wall, which can trigger the human immune system. Polymorphisms in the genes encoding for the chitin-degrading enzymes chitotriosidase and AMCase were described, resulting in altered chitinase activity. We investigated the association between 4 of these polymorphisms and the incidence of M. mycetomatis mycetoma in a Sudanese population.

Methodology: Polymorphisms studied in 112 eumycetoma patients and 103 matched controls included a 24-bp insertion in the chitotriosidase gene (rs3831317), resulting in impaired chitinase activity and single nucleotide polymorphism (SNP) in the AMCase gene (rs61756687), resulting in decreased AMCase activity. Also, a SNP (rs41282492) and a 10-bp insertion in the 5'UTR region of the AMCase gene (rs143789088) were studied, both resulting in increased AMCase activity. DNA was isolated from blood and genotypes were determined using PCR-RFLP.

Principal findings: Histological staining proved the presence of chitin in the fungal grain. The polymorphism resulting in decreased chitotriosidase activity was associated with increased odds of eumycetoma (odds ratio 2.9; p = 0.004). No association was found for the polymorphisms in the genes for AMCase (all p>0.05).

Conclusion: Decreased chitotriosidase activity was associated with increased risk of M. mycetomatis mycetoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Female
  • Genotype*
  • Hexosaminidases / genetics*
  • Hexosaminidases / metabolism*
  • Humans
  • Infant
  • Madurella / isolation & purification*
  • Male
  • Mycetoma / epidemiology*
  • Mycetoma / microbiology
  • Mycetoma / pathology*
  • Polymorphism, Genetic*
  • Retrospective Studies
  • Risk Assessment
  • Sudan / epidemiology
  • Young Adult

Substances

  • Hexosaminidases
  • chitotriosidase

Grants and funding

WWJvdS was supported by VENI grant 916.11.178 from the Netherlands Society of Scientific Research (NWO). The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.