tetano
Editor, Senior Moderator
Viruses
. 2020 Sep 27;12(10):E1095.
doi: 10.3390/v12101095.
Host Immune Response Driving SARS-CoV-2 Evolution
Rui Wang[SUP] 1 [/SUP], Yuta Hozumi[SUP] 1 [/SUP], Yong-Hui Zheng[SUP] 2 [/SUP], Changchuan Yin[SUP] 3 [/SUP], Guo-Wei Wei[SUP] 1 4 5 [/SUP]
Affiliations
Abstract
The transmission and evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are of paramount importance in controlling and combating the coronavirus disease 2019 (COVID-19) pandemic. Currently, over 15,000 SARS-CoV-2 single mutations have been recorded, which have a great impact on the development of diagnostics, vaccines, antibody therapies, and drugs. However, little is known about SARS-CoV-2's evolutionary characteristics and general trend. In this work, we present a comprehensive genotyping analysis of existing SARS-CoV-2 mutations. We reveal that host immune response via APOBEC and ADAR gene editing gives rise to near 65% of recorded mutations. Additionally, we show that children under age five and the elderly may be at high risk from COVID-19 because of their overreaction to the viral infection. Moreover, we uncover that populations of Oceania and Africa react significantly more intensively to SARS-CoV-2 infection than those of Europe and Asia, which may explain why African Americans were shown to be at increased risk of dying from COVID-19, in addition to their high risk of COVID-19 infection caused by systemic health and social inequities. Finally, our study indicates that for two viral genome sequences of the same origin, their evolution order may be determined from the ratio of mutation type, C > T over T > C.
Keywords: ADAR; APOBEC; COVID-19; SARS-CoV-2; gene editing.
. 2020 Sep 27;12(10):E1095.
doi: 10.3390/v12101095.
Host Immune Response Driving SARS-CoV-2 Evolution
Rui Wang[SUP] 1 [/SUP], Yuta Hozumi[SUP] 1 [/SUP], Yong-Hui Zheng[SUP] 2 [/SUP], Changchuan Yin[SUP] 3 [/SUP], Guo-Wei Wei[SUP] 1 4 5 [/SUP]
Affiliations
- PMID: 32992592
- DOI: 10.3390/v12101095
Abstract
The transmission and evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are of paramount importance in controlling and combating the coronavirus disease 2019 (COVID-19) pandemic. Currently, over 15,000 SARS-CoV-2 single mutations have been recorded, which have a great impact on the development of diagnostics, vaccines, antibody therapies, and drugs. However, little is known about SARS-CoV-2's evolutionary characteristics and general trend. In this work, we present a comprehensive genotyping analysis of existing SARS-CoV-2 mutations. We reveal that host immune response via APOBEC and ADAR gene editing gives rise to near 65% of recorded mutations. Additionally, we show that children under age five and the elderly may be at high risk from COVID-19 because of their overreaction to the viral infection. Moreover, we uncover that populations of Oceania and Africa react significantly more intensively to SARS-CoV-2 infection than those of Europe and Asia, which may explain why African Americans were shown to be at increased risk of dying from COVID-19, in addition to their high risk of COVID-19 infection caused by systemic health and social inequities. Finally, our study indicates that for two viral genome sequences of the same origin, their evolution order may be determined from the ratio of mutation type, C > T over T > C.
Keywords: ADAR; APOBEC; COVID-19; SARS-CoV-2; gene editing.