ISG15
干扰素
维罗细胞
基因
干扰素刺激基因
生物
病毒学
干扰素基因刺激剂
2019年冠状病毒病(COVID-19)
分泌物
免疫学
病毒
遗传学
医学
免疫系统
先天免疫系统
传染病(医学专业)
疾病
病理
生物化学
泛素
作者
Yaolin Guo,Caiqin Yang,Yongjian Liu,Tianyi Li,Hanping Li,Jingwan Han,Lei Jia,Xiaolin Wang,Bohan Zhang,Jingyun Li,Lin Li
出处
期刊:Viruses
[Multidisciplinary Digital Publishing Institute]
日期:2022-05-07
卷期号:14 (5): 996-996
被引量:17
摘要
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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