Why the study?
Interferon is disordered in COVID-19 patients, and ERV can affect interferon secretion via the cGAS-STING pathway, but whether IFN-I and HERV-K (HML-2) are activated and interact in COVID-19 patients was unknown.
High expression of HERV-K (HML-2) in COVID-19 patients is associated with increased interferon-related gene expression, suggesting a potential role in host antiviral immunity.
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HERV-K expression may associate with IFN-I changes in COVID-19; leaves open causal role and clinical relevance pending prospective validation.
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.
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Guo et al. (2022) studied this question.
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