Background.
Interferon is a marker of host
antiviral immunity, which is disordered in
COVID-19 patients. ERV can affect the secretion of
interferon through the cGAS-
STING pathway. In this study, we explored whether IFN-I and HERV-K (HML-2) were activated in
COVID-19 patients and whether there was an interaction between them. Methods. We collected blood samples from
COVID-19 patients and healthy controls. We first detected the expression of HERV-K (HML-2) gag, env, and pol genes and IFN-I-related genes between patients and healthy people by qPCR, synchronously detected VERO cells infected with SARS-CoV-2. Then, the chromosome distributions of highly expressed HERV-K (HML-2) gag, env, and pol genes were mapped by the next-generation sequencing results, and GO analysis was performed on the related genes. Results. We found that the HERV-K (HML-2) gag, env, and pol genes were highly expressed in
COVID-19 patients and VERO cells infected with SARS-CoV-2. The
interferon-related genes IFNB1, ISG15, and IFIT1 were also activated in
COVID-19 patients, and GO analysis showed that HERV-K (HML-2) can regulate the secretion of
interferon. Conclusions. The high expression of HERV-K (HML-2) might activate the increase of
interferon in
COVID-19 patients, proving that HERV-K does not only play a negative role in the human body.