Evidence map›Paper›PMID 41331631›Full record

ArticleMalaria journal2025

Preliminary analysis of the conserved Plasmodium falciparum k13 gene in Arbaminch and Mirab Abaya, Ethiopia.

Kefiyalew Jote, Yirgalem Gebrehiwot, Abnet Abebe, Canelle Kipayko, Cheikh Cambel Dieng, Eugenia Lo, Lemu Golassa, Bayissa Chala

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Article in Malaria journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Kefiyalew JoteDepartment of Applied Biology, Adama Science and Technology University, Adama, Ethiopia. kefiyalewjote@gmail.com.
Yirgalem GebrehiwotInstitute of Pathobiology, Addis Ababa University, Addis Ababa, Ethiopia.
Abnet AbebeEthiopian Public Health Institute, Addis Ababa, Ethiopia.
Canelle KipaykoDepartment of Microbiology and Immunology, College of Medicine, Drexel University, Philadelphia, USA.
Cheikh Cambel DiengDepartment of Microbiology and Immunology, College of Medicine, Drexel University, Philadelphia, USA.
Eugenia LoDepartment of Microbiology and Immunology, College of Medicine, Drexel University, Philadelphia, USA.
Lemu GolassaInstitute of Pathobiology, Addis Ababa University, Addis Ababa, Ethiopia.
Bayissa ChalaDepartment of Applied Biology, Adama Science and Technology University, Adama, Ethiopia.

Funding

Plasmodium vivax Erythrocyte Invasion Mechanisms and Humoral Immune Response in Duffy Negative AfricansR01AI162947 · NIAID · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI Eugenia Lo · 2022 to 2026
$3.4M
NIAID NIH HHS R01 AI162947
6 · The paper itself

Abstract

backgroundReports from East and Horn of Africa showed artemisinin resistance is threatening control efforts. The Pfkelch13 (k13) gene mutation in Plasmodium falciparum is essential for tracking artemisinin resistance, which significantly jeopardizes malaria treatment effectiveness. The objective of this study was to assess the occurrence and prevalence of k13 gene polymorphisms at selected public health facilities of Arbaminch and Mirab Abaya, Ethiopia.

methodsA cross-sectional study was conducted in Arbaminch and Mirab Abaya from May to December 2023. A total of 52 P. falciparum mono-infection samples confirmed by PCR were analysed. Sanger sequencing was used to obtain the sequences of k13 gene propeller domain, and phylogenetic analysis was performed using Molecular Evolutionary Genetic Analysis software version 11. Gene flow and differentiation were analysed with DnaSP6, while sequences from six other African countries were included from global database for haplotype network analysis using PopART 1.7.

resultsAmong the 52 participants, 28 (52.8%) were male and 24 (47.2%) were female. The median age was 19 years old with an interquartile range of 15 to 32 years. There was no polymorphism identified in the studied samples indicating high genetic conservation (pairwise similarity index = 0.982). Isolates from Mirab Abaya exhibited strong genetic homogeneity, while Arbaminch samples showed slight divergence and yet remained largely conserved. Ethiopian haplotypes contributed significantly to a dominant African haplotype, with no k13 mutations detected. Although mild genetic diversity was observed in some African countries, haplotype and nucleotide diversity were not statistically significant. A negative Fu and Li's D statistic was observed, suggesting that low-frequency mutations could be due to selective sweep in the parasite population.

conclusionThis study found no evidence of P. falciparum k13 gene mutations in isolates from Arbaminch and Mirab Abaya, indicating a high level of genetic conservation. Although minor genetic divergence was observed, particularly among Arbaminch isolates, the overall population remained genetically homogeneous. These findings highlight the continued effectiveness of artemisinin-based combination therapy in the region and emphasize the need for ongoing molecular surveillance to monitor potential resistance emergence.

Indexed as

Malaria, FalciparumPlasmodium falciparumPolymorphism, GeneticProtozoan ProteinsAdolescentAdultCross-Sectional StudiesDrug ResistanceEthiopiaFemaleHumansMalePhylogenyYoung AdultProtozoan ProteinsArbaminchHaplotypekelch13 geneMutationP. falciparum

Identifiers

PMID41331631
PMCPMC12777202

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