Plasminogen alleles influence susceptibility to invasive aspergillosis.

Journal Article (Journal Article)

Invasive aspergillosis (IA) is a common and life-threatening infection in immunocompromised individuals. A number of environmental and epidemiologic risk factors for developing IA have been identified. However, genetic factors that affect risk for developing IA have not been clearly identified. We report that host genetic differences influence outcome following establishment of pulmonary aspergillosis in an exogenously immune suppressed mouse model. Computational haplotype-based genetic analysis indicated that genetic variation within the biologically plausible positional candidate gene plasminogen (Plg; Gene ID 18855) correlated with murine outcome. There was a single nonsynonymous coding change (Gly110Ser) where the minor allele was found in all of the susceptible strains, but not in the resistant strains. A nonsynonymous single nucleotide polymorphism (Asp472Asn) was also identified in the human homolog (PLG; Gene ID 5340). An association study within a cohort of 236 allogeneic hematopoietic stem cell transplant (HSCT) recipients revealed that alleles at this SNP significantly affected the risk of developing IA after HSCT. Furthermore, we demonstrated that plasminogen directly binds to Aspergillus fumigatus. We propose that genetic variation within the plasminogen pathway influences the pathogenesis of this invasive fungal infection.

Full Text

Duke Authors

Cited Authors

  • Zaas, AK; Liao, G; Chien, JW; Weinberg, C; Shore, D; Giles, SS; Marr, KA; Usuka, J; Burch, LH; Perera, L; Perfect, JR; Peltz, G; Schwartz, DA

Published Date

  • June 20, 2008

Published In

Volume / Issue

  • 4 / 6

Start / End Page

  • e1000101 -

PubMed ID

  • 18566672

Pubmed Central ID

  • PMC2423485

Electronic International Standard Serial Number (EISSN)

  • 1553-7404

Digital Object Identifier (DOI)

  • 10.1371/journal.pgen.1000101


  • eng

Conference Location

  • United States