Coinfection. Virus-helminth coinfection reveals a microbiota-independent mechanism of immunomodulation

Science. 2014 Aug 1;345(6196):578-82. doi: 10.1126/science.1256942. Epub 2014 Jul 17.

Abstract

The mammalian intestine is colonized by beneficial commensal bacteria and is a site of infection by pathogens, including helminth parasites. Helminths induce potent immunomodulatory effects, but whether these effects are mediated by direct regulation of host immunity or indirectly through eliciting changes in the microbiota is unknown. We tested this in the context of virus-helminth coinfection. Helminth coinfection resulted in impaired antiviral immunity and was associated with changes in the microbiota and STAT6-dependent helminth-induced alternative activation of macrophages. Notably, helminth-induced impairment of antiviral immunity was evident in germ-free mice, but neutralization of Ym1, a chitinase-like molecule that is associated with alternatively activated macrophages, could partially restore antiviral immunity. These data indicate that helminth-induced immunomodulation occurs independently of changes in the microbiota but is dependent on Ym1.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / immunology
  • Caliciviridae Infections / immunology*
  • Coinfection / immunology*
  • Coinfection / microbiology
  • Coinfection / parasitology
  • Gastroenteritis / immunology*
  • Gastroenteritis / virology
  • Germ-Free Life
  • Immunomodulation*
  • Intestines / immunology
  • Intestines / microbiology
  • Intestines / virology
  • Lectins / immunology*
  • Macrophage Activation
  • Macrophages / immunology
  • Mice
  • Mice, Inbred C57BL
  • Microbiota / immunology*
  • Norovirus / immunology*
  • Trichinella / immunology*
  • Trichinellosis / immunology*
  • beta-N-Acetylhexosaminidases / immunology*

Substances

  • Lectins
  • Chil3 protein, mouse
  • beta-N-Acetylhexosaminidases

Associated data

  • SRA/SRP043964

Grants and funding