Increased susceptibility to Strongyloides venezuelensis in mice due to Mycobacterium bovis co-infection which modulates production of Th2 cytokines

Parasitology. 2009 Sep;136(11):1357-65. doi: 10.1017/S0031182009990655. Epub 2009 Aug 7.

Abstract

An estimated quarter of the world's population possesses an infection caused by gastrointestinal nematodes, which induce a Th2 type immune response. Concomitant infection of nematodes with Mycobacterium tuberculosis, which induces a predominantly Th1 type response, is very frequent in tropical and subtropical regions. This study examined immune responses of BALB/c mice infected with Strongyloides venezuelensis and then co-infected with Mycobacterium bovis. The number of worms in the intestine, eggs in feces, cytokine production in lungs and intestine and the expression of CD80, CD86, CTLA-4 and CD28 cell markers on pulmonary cells were analysed. Our results indicate that co-infected mice had an increased parasite burden, which correlates with elevated IFN-gamma and IL-10 cytokine production and decreased IL-4 and IL-13. Moreover, decreased expression of CD80 and increased expression of CTLA-4 were observed in co-infected mice. Our data point out that susceptibility to Strongyloides venezuelensis infection is increased by Mycobacterium bovis co-infection, resulting in higher parasite survival.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cytokines / metabolism*
  • Disease Susceptibility
  • Feces / parasitology
  • Interferon-gamma / metabolism
  • Interleukin-10 / metabolism
  • Intestines / immunology
  • Intestines / parasitology
  • Lung / immunology
  • Lung / parasitology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mycobacterium Infections / complications*
  • Mycobacterium Infections / immunology
  • Mycobacterium Infections / microbiology
  • Mycobacterium bovis* / immunology
  • Mycobacterium bovis* / pathogenicity
  • Parasite Egg Count
  • Rats
  • Rats, Wistar
  • Strongyloides / classification
  • Strongyloides / pathogenicity*
  • Strongyloidiasis / complications*
  • Strongyloidiasis / immunology
  • Strongyloidiasis / parasitology
  • Th2 Cells / immunology*

Substances

  • Cytokines
  • Interleukin-10
  • Interferon-gamma