Genetic diversity and spread dynamics of SARS-CoV-2 variants present in African populations

Dataset mining and workflow SARS-CoV-2 genome sequences collected from Africa were obtained from NCBI database and GISAID database on February 26, 2023. 24415 African sequences were retrieved from both databases so as to examine the number of lineages circulating within Africa. The two databases had only 8044 complete genome sequences combined from Africa, and these sequences excluding those with low coverage using NextClade were retrieved to determine spread dynamics. 5908 sequences from 23 African countries were available in the NCBI and 2137 sequences from 41 African countries from GISAID database. The sequences were aligned using the online version of the MAFFT multiple sequence alignment tool, with the Wuhan-Hu-1 (MN 908947.3) as the reference sequence, and sequences with more than 5.0% ambiguous letters were removed. Duplicates were removed using goalign dedup software and only high quality African complete sequences remained (n=7540). Phylogenetic reconstruction Using IQ-TREE multicore software version v1.6.12 and NextClade, phylogeny reconstruction on the dataset was performed numerous times. Lineage classification PANGOLin, a web application was used to classify sequences into their lineages. The objective was to determine the SARS-CoV-2 lineages that are circulating in Africa that are most important from an epidemiological perspective, as well as the lineage dynamics within and across the African continent, due to the fact that this naming system integrates genetic and geographic data concerning SARS-CoV-2 dynamics. Phylogeographic reconstruction VOC, (VOI) and VUM were designated based on the WHO framework as of 20 January 2022. We included one lineage, namely A.23.1 and labelled it as VOI for the purposes of this analysis. This lineage was included because it demonstrated the continued evolution of African lineages into potentially more transmissible variants. VOI, VOC, and VUM that emerged on the African continent were marked. These were A.23.1 (VOI), B.1.351 and B.1.1.529 (VOC), B.1.640, and B.1.525 (VUM). Genome sequences of these five lineages were extracted from NCBI database for phylogeographic reconstruction. A similar approach to that described above (including alignment using online MAFFT) was employed. Phylogeographic reconstruction for all variants circulating in Africa and all VOI, VOC, and VUM was conducted using PASTML.