| Literature DB >> 28368463 |
Lisa A Reynolds1,2, Stephen A Redpath3, Sophie Yurist-Doutsch1, Navkiran Gill1, Eric M Brown1,3, Joris van der Heijden1,3, Tara P Brosschot1, Jun Han4, Natalie C Marshall1,3, Sarah E Woodward1,3, Yanet Valdez1, Christoph H Borchers2,4,5,6, Georgia Perona-Wright3,7, B Brett Finlay1,3,8.
Abstract
Intestinal helminth infections occur predominantly in regions where exposure to enteric bacterial pathogens is also common. Helminth infections inhibit host immunity against microbial pathogens, which has largely been attributed to the induction of regulatory or type 2 (Th2) immune responses. Here we demonstrate an additional 3-way interaction in which helminth infection alters the metabolic environment of the host intestine to enhance bacterial pathogenicity. We show that an ongoing helminth infection increased colonization by Salmonella independently of T regulatory or Th2 cells. Instead, helminth infection altered the metabolic profile of the intestine, which directly enhanced bacterial expression of Salmonella pathogenicity island 1 (SPI-1) genes and increased intracellular invasion. These data reveal a novel mechanism by which a helminth-modified metabolome promotes susceptibility to bacterial coinfection.Entities:
Keywords: bacterial infection; co-infection; helminths; immunomodulation; intestinal metabolites.
Mesh:
Year: 2017 PMID: 28368463 PMCID: PMC5853568 DOI: 10.1093/infdis/jix141
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226