Key Host Mechanism Found To Fuel Coronavirus Growth

By using live-cell microscopy, quantitative immunofluorescence, and biochemical analyses, the researchers were able to demonstrate that JNK is specifically activated in infected cells. They used a kinase translocation reporter (KTR) to directly visualize the marked increase in JNK activity approximately 16 hours after infection. If the kinase is blocked by specific inhibitors, virus production was reduced significantly. This is the case for both HcoV-229E and SARS-CoV-2.

In cooperation with the group led by Professor Michael Kracht at University of Giessen, the team was also able to show that JNK phosphorylates specific serine residues on the N protein. These sites are conserved in various coronaviruses, indicating that JNK plays a joint role in the replication of various virus types. “Our data highlight JNK as an important host factor that is directly involved in the modification of the N protein, a critical step in virus replication,” explains Brüggemann. “The fact that inhibition of JNK hampers the replication of both HCoV-229E and SARS-CoV-2 shows the potential of this signal pathway as a future starting point for new antiviral agents,” adds Steinmann.

Reference: Brüggemann Y, Meister TL, Heinen N, et al. JNK kinase regulates phosphorylation of HCoV-229E nucleocapsid protein. npj Viruses. 2025;3(1):69. doi:10.1038/s44298-025-00152-7

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