Association of specific ACE2 and TMPRSS2 variants with circulatory cytokines of COVID-19 Emirati patients

特定 ACE2 和 TMPRSS2 变体与 COVID-19 阿联酋患者循环细胞因子的关联

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作者:Noha M Elemam #, Amal Bouzid #, Habiba Alsafar, Samrein Bm Ahmed, Shirin Hafezi, Thenmozhi Venkatachalam, Leen Eldohaji, Tasneem Al Hamidi, Peter Habib Gerges, Nour Halabi, Hassen Hadj-Kacem, Iman M Talaat, Jalal Taneera, Nabil Sulaiman, Azzam A Maghazachi, Qutayba Hamid, Rifat Hamoudi, Maha Saber-A

Conclusion

Whereas COVID-19 represents now a past pandemic, our study underscores the importance of genetic factors specific to a population, which can influence both the susceptibility to viral infections and the level of severity; subsequently expected required preparedness in different areas of the world.

Methods

We compiled a panel of gene variants from both genes and used in-silico analysis to predict their significance. We performed biological validation to assess their capacity to alter the ACE2 interaction with the virus spike protein. Subsequently, we conducted a retrospective comparative genome analysis on those variants in the Emirati patients with different disease severity (total of 96) along with 69 healthy control subjects.

Results

Our results showed that the Emirati population lacks the variants that were previously reported as associated with disease severity, whereas a new variant in ACE2 "Chr X:g.15584534" was associated with disease severity specifically among female patients. In-silico analysis revealed that the new variant can determine the ACE2 gene transcription. Several cytokines (GM-CSF and IL-6) and chemokines (MCP-1/CCL2, IL-8/CXCL8, and IP-10/CXCL10) were markedly increased in COVID-19 patients with a significant correlation with disease severity. The newly reported genetic variant of ACE2 showed a positive correlation with CD40L, IL-1β, IL-2, IL-15, and IL-17A in COVID-19 patients.

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