Authors: Ingle, Harshad; Hassan, Ebrahim; Gawron, Jana; Mihi, Belgacem; Li, Yuhao; Kennedy, Elizabeth A.; Kalugotla, Gowri; Makimaa, Heyde; Lee, Sanghyun; Desai, Pritesh; McDonald, Keely G.; Diamond, Michael S.; Newberry, Rodney D.; Good, Misty; Baldridge, Megan T.
Issue: Mucosal Immunol . 2021 May;14(3):751-761.
Although they globally cause viral gastroenteritis in children, astroviruses are understudied due to the lack of well-defined animal models. While murine astroviruses (muAstVs) chronically infect immunodeficient mice, a culture system and understanding of their pathogenesis is lacking. Here, we describe a platform to cultivate muAstV using air–liquid interface (ALI) cultures derived from mouse enteroids, which support apical infection and release. Chronic muAstV infection occurs predominantly in the small intestine and correlates with higher interferon-lambda (IFN-λ) expression. MuAstV stimulates IFN-λ production in ALI, recapitulating our in vivo findings. We demonstrate that goblet cells and enterocytes are targets for chronic muAstV infection in vivo, and that infection is enhanced by parasite co-infection or type 2 cytokine signaling. Depletion of goblet cells from ALI limits muAstV infection in vitro. During chronic infection, muAstV stimulates IFN-λ production in infected cells and induces ISGs throughout the intestinal epithelium in an IFN-λ-receptor-dependent manner. Collectively, our study provides insights into the cellular tropism and innate immune responses to muAstV and establishes an enteroid-based culture system to propagate muAstV in vitro.