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Viral complementation of immunodeficiency confers protection against enteric pathogens via interferon-λ.

Harshad IngleSanghyun LeeTeresa AiAnthony OrvedahlRachel RodgersGuoyan ZhaoMeagan SullenderStefan T PetersonMarissa C LockeTa-Chiang LiuChristine C YokoyamaBridgett SharpStacey Schultz-CherryJonathan J MinerMegan T Baldridge
Published in: Nature microbiology (2019)
Commensal microbes profoundly impact host immunity to enteric viral infections1. We have shown that the bacterial microbiota and host antiviral cytokine interferon-λ (IFN-λ) determine the persistence of murine norovirus in the gut2,3. However, the effects of the virome in modulating enteric infections remain unexplored. Here, we report that murine astrovirus can complement primary immunodeficiency to protect against murine norovirus and rotavirus infections. Protection against infection was horizontally transferable between immunocompromised mouse strains by co-housing and fecal transplantation. Furthermore, protection against enteric pathogens corresponded with the presence of a specific strain of murine astrovirus in the gut, and this complementation of immunodeficiency required IFN-λ signalling in gut epithelial cells. Our study demonstrates that elements of the virome can protect against enteric pathogens in an immunodeficient host.
Keyphrases
  • dendritic cells
  • gram negative
  • sars cov
  • immune response
  • antimicrobial resistance
  • signaling pathway
  • stem cells
  • multidrug resistant
  • intensive care unit