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SARS-CoV-2 mutations on diagnostic gene targets in the second wave in Zimbabwe: A retrospective genomic analysis.

Authors :
Nyagupe C
de Oliveira Martins L
Gumbo H
Mashe T
Takawira T
Maeka KK
Juru A
Chikanda LK
Tauya AR
Page AJ
Kingsley RA
Simbi R
Chirenda J
Manasa J
Ruhanya V
Mavenyengwa RT
Source :
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde [S Afr Med J] 2023 Mar 02; Vol. 113 (3), pp. 141-147. Date of Electronic Publication: 2023 Mar 02.
Publication Year :
2023

Abstract

Background: SARS-CoV-2 continues to be a major issue in resource-limited settings, particularly owing to the limited supply of vaccinescaused by inequitable distribution.<br />Objective: To monitor diagnostic gene targets to identify potential test failures caused by mutations, which is important for public health.<br />Methods: Here we analysed the genome sequence of SARS-CoV-2 from the second wave in Zimbabwe. A total of 377 samples weresequenced at Quadram Institute Bioscience. After quality control, 192 sequences passed and were analysed.<br />Results: The Beta variant was dominant during this period, contributing 77.6% (149) of the genomes sequenced and having a total of 2994mutations in diagnostic polymerase chain reaction target genes. Many single nucleotide polymorphism mutations resulted in amino acidsubstitution that had the potential to impact viral fitness by increasing the rate of transmission or evading the immune response to previousinfection or vaccination.<br />Conclusion: There were nine lineages circulating in Zimbabwe during the second wave. The B.1.351 was dominant, accounting for >75%.There were over 3 000 mutations on the diagnostic genes and lineage B.1.351, contributing almost two-thirds of the mutations. The S-genehad the most mutations and the E-gene was the least mutated.

Details

Language :
English
ISSN :
2078-5135
Volume :
113
Issue :
3
Database :
MEDLINE
Journal :
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde
Publication Type :
Academic Journal
Accession number :
36876349
Full Text :
https://doi.org/10.7196/SAMJ.2023.v113i3.16762