Regulatory variants of APOBEC3 genes potentially associate with COVID-19 severity in populations with African ancestry
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Updated: Jul 8, 2025

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
Ke Zhang1, Fang Chen1, Hu-Yan Shen1
1The Key and Characteristic Laboratory of Modern Pathogenicity Biology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang, 561113, China.
Insights
Genetic variants in APOBEC3 genes may increase COVID-19 hospitalization risk in African populations due to higher SARS-CoV-2 mutation rates. Further research is needed to confirm these findings on coronavirus evolution.
Area of Science:
- Genetics
- Virology
- Epidemiology
Background:
- The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has had a profound global impact.
- Ongoing SARS-CoV-2 mutations complicate control efforts, with C>U nucleotide substitutions linked to human APOBEC3 gene editing.
- Specific SARS-CoV-2 variants like Beta and Omicron, first observed in South Africa, exhibit high mutation rates.
Purpose of the Study:
- To investigate the hypothesis that APOBEC3 gene variants in African populations contribute to higher SARS-CoV-2 mutation rates.
- To identify functional APOBEC3 gene variants associated with COVID-19 hospitalization in the African population.
Main Methods:
- Integrated data from the 1000 Genomes Project, Genotype-Tissue Expression (GTEx), and Host Genetics Initiative (HGI).
- Analyzed genetic data to find single nucleotide polymorphisms (SNPs) near APOBEC3 genes.
- Compared associations between identified SNPs and COVID-19 hospitalization across different populations.
Main Results:
- Identified potential functional SNPs near APOBEC3 genes associated with COVID-19 hospitalization.
- These associations were specific to the African population and not observed in other populations.
- Suggests a potential role of APOBEC3 genes in SARS-CoV-2 evolution within African populations.
Conclusions:
- APOBEC3 genes may influence SARS-CoV-2 evolution and COVID-19 outcomes in African populations.
- The findings offer new insights into the genetic factors affecting viral mutation rates.
- Further replication studies are necessary to validate these results.
Abstract:
Since November 2019, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has caused the worldwide pandemic of the coronavirus disease 2019 (COVID-19), the impact of which is huge to the lives of world populations. Many studies suggested that such situation will continue due to the endless mutations in SARS-CoV-2 genome that result in complexity of the efforts for the control of SARS-CoV-2, since the special enrichment of nucleotide substitution C>U in SARS-CoV-2 sequences were discovered mainly due to the editing by human host factors APOBEC3 genes. The observation of SARS-CoV-2 variants Beta (B.1.351) and Omicron (B.1.1.529) firstly spreading in South Africa promoted us to hypothesize that genetic variants of APOBEC3 special in African populations may be attributed to the higher mutation rate of SARS-CoV-2 variants in Africa. Current study was conducted to search for functional variants of APOBEC3 genes associate with COVID-19 hospitalization in African population. By integrating data from the 1000 Genomes Project, Genotype-Tissue Expression (GTEx), and Host Genetics Initiative (HGI) of COVID-19, we identified potential functional SNPs close to APOBEC3 genes that are associated with COVID-19 hospitalization in African but not with other populations. Our study provides new insights on the potential contribution of APOBEC3 genes on the evolution of SARS-CoV-2 mutations in African population, but further replication is needed to confirm our results.
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