Characterization of innate responses to influenza virus infection in a novel lung type I epithelial cell model

Author:

Rosenberger Carrie M.1,Podyminogin Rebecca L.1,Askovich Peter S.1,Navarro Garnet1,Kaiser Shari M.1,Sanders Catherine J.1,McClaren Jennifer L.2,Tam Vincent C.1,Dash Pradyot1,Noonan Jhoanna G.1,Jones Bart G.3,Surman Sherri L.3,Peschon Jacques J.1,Diercks Alan H.1,Hurwitz Julia L.3,Doherty Peter C.2,Thomas Paul G.2,Aderem Alan1

Affiliation:

1. Seattle Biomedical Research Institute, 307 Westlake Avenue North, Suite 500, Seattle, WA 98109, USA

2. Department of Immunology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105-3678, USA

3. Department of Infectious Diseases, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105-3678, USA

Abstract

Type I alveolar epithelial cells are a replicative niche for influenza in vivo, yet their response to infection is not fully understood. To better characterize their cellular responses, we have created an immortalized murine lung epithelial type I cell line (LET1). These cells support spreading influenza virus infection in the absence of exogenous protease and thus permit simultaneous analysis of viral replication dynamics and host cell responses. LET1 cells can be productively infected with human, swine and mouse-adapted strains of influenza virus and exhibit expression of an antiviral transcriptional programme and robust cytokine secretion. We characterized influenza virus replication dynamics and host responses of lung type I epithelial cells and identified the capacity of epithelial cell-derived type I IFN to regulate specific modules of antiviral effectors to establish an effective antiviral state. Together, our results indicate that the type I epithelial cell can play a major role in restricting influenza virus infection without contribution from the haematopoietic compartment.

Publisher

Microbiology Society

Subject

Virology

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