Genetic evidence for the role of the Lv locus in early susceptibility but not IL-10 synthesis in experimental coccidioidomycosis in C57BL mice

J Infect Dis. 2000 Feb;181(2):681-5. doi: 10.1086/315256.

Abstract

Loci on chromosome 4 near Lv and on chromosome 6 near Tnfr1 are associated with resistance to coccidioidomycosis in mice. To assess the importance of the Lv locus, we compared C57BL/6 (B6) with C57BL/10 (B10), strains that are nearly congenic for the Lv locus. Fourteen days after intraperitoneal infection, B6 mice had nearly 100-fold more Coccidioides immitis in their lungs than did B10 mice (log 6.2 vs. log 4.8). Furthermore, the time to 50% deaths was 15 days for B6 and 22 days for B10. Nevertheless, 90% of B10 mice had died by day 28. In other mouse strains, we found a direct correlation between lung colony-forming units and levels of interleukin (IL)-10 and IL-4 mRNA, but B10 mice had 100-fold higher lung levels of IL-10 and 10-fold higher levels of IL-4 mRNA than did B6 mice, despite having less C. immitis. In the absence of IL-10, B10 mice are resistant to lethal infection. These results suggest that a locus near Lv is responsible for early resistance to coccidioidomycosis but not for modulating the IL-10 and IL-4 responses. This locus is not sufficient to make C57BL mice resistant to coccidioidomycosis.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Chromosome Mapping
  • Chromosomes / genetics
  • Coccidioides / isolation & purification*
  • Coccidioidomycosis / genetics*
  • Coccidioidomycosis / immunology*
  • Coccidioidomycosis / microbiology
  • Coccidioidomycosis / mortality
  • Female
  • Genetic Predisposition to Disease*
  • Interleukin-10 / biosynthesis*
  • Interleukin-10 / genetics
  • Interleukin-4 / biosynthesis
  • Interleukin-4 / genetics
  • Lung / microbiology
  • Mice
  • Mice, Inbred C57BL
  • Phenotype
  • Polymerase Chain Reaction / methods
  • Receptors, Tumor Necrosis Factor / genetics

Substances

  • Receptors, Tumor Necrosis Factor
  • Interleukin-10
  • Interleukin-4