IFN-λ determines the intestinal epithelial antiviral host defense

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 108; no. 19; pp. 7944 - 7949
• Main Authors: Pott, Johanna, Mahlakõiv, Tanel, Mordstein, Markus, Duerr, Claudia U., Michiels, Thomas, Stockinger, Silvia, Staeheli, Peter, Hornef, Mathias W., Hiscott, John
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 10.05.2011; National Acad Sciences
• Subjects: adults; Animals; Antigens; Antivirals; Biological Sciences; Cytokines - immunology; Digestive tract; Epithelial cells; Gene expression; Immune response; Immunity, Innate; Infection; Infections; innate immunity; Interferon; Interferons; intestinal mucosa; Intestinal Mucosa - immunology; Intestinal Mucosa - pathology; Intestinal Mucosa - virology; Intestine; Mice; Mice, Inbred C57BL; Mice, Knockout; Mucosa; Myxovirus resistance proteins; Receptor, Interferon alpha-beta - deficiency; Receptor, Interferon alpha-beta - genetics; Receptor, Interferon alpha-beta - immunology; Receptors; Replication; Rotavirus; Rotavirus - immunology; Rotavirus - physiology; Rotavirus infections; Rotavirus Infections - immunology; Rotavirus Infections - pathology; Rotavirus Infections - prevention & control; Rotavirus Infections - virology; Signal transduction; Signal Transduction - immunology; suckling; Suckling behavior; Virus Replication; Viruses
• ISSN: 0027-8424; 1091-6490; 1091-6490
• DOI: 10.1073/pnas.1100552108

Type I and type III IFNs bind to different cell-surface receptors but induce identical signal transduction pathways, leading to the expression of antiviral host effector molecules. Despite the fact that type III IFN (IFN-λ) has been shown to predominantly act on mucosal organs, in vivo infection studies have failed to attribute a specific, nonredundant function. Instead, a predominant role of type I IFN was observed, which was explained by the ubiquitous expression of the type I IFN receptor. Here we comparatively analyzed the role of functional IFN-λ and type I IFN receptor signaling in the innate immune response to intestinal rotavirus infection in vivo, and determined viral replication and antiviral gene expression on the cellular level. We observed that both suckling and adult mice lacking functional receptors for IFN-λ were impaired in the control of oral rotavirus infection, whereas animals lacking functional receptors for type I IFN were similar to wild-type mice. Using Mx1 protein accumulation as marker for IFN responsiveness of individual cells, we demonstrate that intestinal epithelial cells, which are the prime target cells of rotavirus, strongly responded to IFN-λ but only marginally to type I IFN in vivo. Systemic treatment of suckling mice with IFN-λ repressed rotavirus replication in the gut, whereas treatment with type I IFN was not effective. These results are unique in identifying a critical role of IFN-λ in the epithelial antiviral host defense.