Published in Virology: a new cell line permissive to human coronavirus 229E
The CARE partner Jagiellonian University (JU) developed a new cell line that can be infected by the human coronavirus 229E (HCoV-229E), a member of the alphacoronavirus family. HCoV-229E is one of the coronaviruses that poorly propagate in cell lines and require extensive cell culture adaptation leading to changes in the virus phenotype. New cell lines are thus necessary to study in vitro HCoV-229E more easily.
To create this new cell line, JU co-transduced CD13 and transmembrane serine protease 2 (TMPRSS2) in A549 cell line (lung-derived cell line) using lentiviral vectors. HCoV-229E can use several pathways to enter a permissive cell, one using CD13, an aminopeptidase N while another one is using TMPRSS2 to proteolytically prime the viral spike, leading to membrane fusion. Cells overexpressing CD13 and TMPRSS2 (A549++ cells) and infected by HCoV-229 showed viral RNA replication and a significant rise on virus titer, confirming their ability to produce infectious HCoV-229E progeny.
Moreover, JU evaluated the possible entry pathways of HCoV-229E in A549++ cells by inhibiting the TMPRSS2-mediated membrane fusion entry pathway and/or the endocytic pathway. The results indicate that although HCoV-229E prefers TMPRSS2-mediated entry, it can also readily use the endocytic pathway in the absence of TMPRSS2.
JU has thus developed a robust and physiologically relevant cell line model that is permissive to HCoV-229E clinical isolate replication. The data provide further insight into the potential of lentiviral transduction in developing permissive cell models for viral infection studies. Moreover, this line constitutes a uniform platform for studies on multiple members of the coronaviridae family.
To learn more, click here: An engineered A549 cell line expressing CD13 and TMPRSS2 is permissive to clinical isolate of human coronavirus 229E