A genetic screen identifies a protective type III interferon response to Cryptosporidium that requires TLR3 dependent recognition
Open Access
- 18 May 2022
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLOS Pathogens
- Vol. 18 (5) , e1010003
Abstract
Cryptosporidiumis a leading cause of severe diarrhea and diarrheal-related death in children worldwide. As an obligate intracellular parasite,Cryptosporidiumrelies on intestinal epithelial cells to provide a niche for its growth and survival, but little is known about the contributions that the infected cell makes to this relationship. Here we conducted a genome wide CRISPR/Cas9 knockout screen to discover host genes that influenceCryptosporidium parvuminfection and/or host cell survival. Gene enrichment analysis indicated that the host interferon response, glycosaminoglycan (GAG) and glycosylphosphatidylinositol (GPI) anchor biosynthesis are important determinants of susceptibility toC.parvuminfection and impact on the viability of host cells in the context of parasite infection. Several of these pathways are linked to parasite attachment and invasion and C-type lectins on the surface of the parasite. Evaluation of transcript and protein induction of innate interferons revealed a pronounced type III interferon response toCryptosporidiumin human cells as well as in mice. Treatment of mice with IFNλ reduced infection burden and protected immunocompromised mice from severe outcomes including death, with effects that required STAT1 signaling in the enterocyte. Initiation of this type III interferon response was dependent on sustained intracellular growth and mediated by the pattern recognition receptor TLR3. We conclude that host cell intrinsic recognition ofCryptosporidiumresults in IFNλ production critical to early protection against this infection.Keywords
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Funding Information
- National Institute of Allergy and Infectious Diseases (R01AI148249)
- National Institute of Allergy and Infectious Diseases (R01AI148249)
- National Institutes of Health (T32AI007532)
- National Institutes of Health (K99AI137442)
- National Institutes of Health (T32AI007532)
- National Institutes of Health (T32A1055400)
This publication has 103 references indexed in Scilit:
- INTERFEROME v2.0: an updated database of annotated interferon-regulated genesNucleic Acids Research, 2012
- Involvement of Host Cell Integrin α2 in Cryptosporidium parvum InfectionInfection and Immunity, 2012
- IFN-λ determines the intestinal epithelial antiviral host defenseProceedings of the National Academy of Sciences, 2011
- Leishmania RNA Virus Controls the Severity of Mucocutaneous LeishmaniasisScience, 2011
- CDC50 Proteins Are Critical Components of the Human Class-1 P4-ATPase Transport MachineryJournal of Biological Chemistry, 2010
- Salmonella-Directed Recruitment of New Membrane to Invasion Foci via the Host Exocyst ComplexCurrent Biology, 2010
- edgeR: a Bioconductor package for differential expression analysis of digital gene expression dataBioinformatics, 2009
- Roles for NK Cells and an NK Cell-Independent Source of Intestinal Gamma Interferon for Innate Immunity toCryptosporidium parvumInfectionInfection and Immunity, 2009
- The Tyrosine Kinase c-Src Enhances RIG-I (Retinoic Acid-inducible Gene I)-elicited Antiviral SignalingJournal of Biological Chemistry, 2009
- Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profilesProceedings of the National Academy of Sciences, 2005