Key result
Integrin α3 is an essential host factor for non-enveloped hepatitis E virus infection, mediating cellular attachment and entry.
Why the study?
Although enveloped and non-enveloped forms of HEV have been discovered, host factors involved in infection, including receptors, remain to be elucidated.
Integrin α3 is identified as an essential host factor and key molecule for cellular attachment and entry of non-enveloped hepatitis E virus.
Integrin α3 may represent a neHEV entry target; leaves open whether blockade prevents infection in vivo.
Hepatitis E virus (HEV) causes acute and fulminant hepatitis worldwide. Although enveloped (e) and non-enveloped (ne) forms of HEV have been discovered, host factors involved in infection, including receptors, remain to be elucidated. Here, we identified integrin α3 (encoded by ITGA3), a protein that binds and responds to the extracellular matrix, as an essential host factor for HEV infection. Integrin α3 expression was lower in four HEV-non-permissive cell subclones than in an HEV-permissive subclone. ITGA3 knockout cells lost HEV permissibility, suggesting that integrin α3 is critical for HEV infection. Stable expression of integrin α3 in an HEV-non-permissive subclone provided permissibility only to infection by neHEV; expression of integrin α3 lacking the ectodomain did not. Direct interaction between neHEV and the integrin α3 ectodomain was confirmed by co-precipitation using a soluble integrin α3-Fc. These results strongly suggest that integrin α3 is a key molecule for cellular attachment and entry of neHEV.
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Shiota et al. (2019) studied Hepatitis E virus infection. Integrin α3 (ITGA3) knockout or expression vs. Wild-type or HEV-permissive subclones was evaluated on HEV permissibility and infection. Integrin α3 is an essential host factor for non-enveloped hepatitis E virus infection, mediating cellular attachment and entry.
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