Occurrence of pfatpase6 Single Nucleotide Polymorphisms Associated with Artemisinin Resistance among Field Isolates of Plasmodium falciparum in North-Eastern Tanzania
| Autor: | Sakurani Barthazary, Hipolite Tarimo, Debora C. Kajeguka, Jaffu Chilongola, John Lusingu, Robert Kaaya, Tamara Shedrack, Alutu Masokoto, Reginald A. Kavishe, Arnold Ndaro |
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| Rok vydání: | 2015 |
| Předmět: |
Article Subject
Epidemiology Single-nucleotide polymorphism Bioinformatics medicine.disease_cause lcsh:Infectious and parasitic diseases parasitic diseases Medicine Parasite hosting lcsh:RC109-216 Allele Artemisinin Gene Diagnosis & treatment Mutation biology business.industry Plasmodium falciparum medicine.disease biology.organism_classification Virology Infectious Diseases business Malaria Research Article medicine.drug |
| Zdroj: | Malaria Research and Treatment Malaria Research and Treatment, Vol 2015 (2015) |
| Popis: | We aimed to determine the current prevalence of fourP. falciparumcandidate artemisinin resistance biomarkers L263E, E431K, A623E, and S769N in thepfatpase6gene in a high transmission area in Tanzania in a retrospective cross sectional study using 154 archived samples collected from three previous malaria studies in 2010, 2011 and 2013. Mutations inpfatpase6gene were detected in parasite DNA isolated from Dried Blood Spots by using PCR-RFLP. We observed overall allelic frequencies for L263E, E431K, A623E, and S769N to be 5.8% (9/154), 16.2% (25/154), 0.0% (0/154), and 3.9% (6/154). The L263E mutation was not detected in 2010 but occurred at 3.9% and 2.6% in 2011 and 2013 respectively. The L263E mutation showed a significant change of frequency between 2010 and 2011, but not between 2011 and 2013P<0.05. Frequency of E431K was highest of all without any clear trend whereas S769N increased from 2.2% in 2010 to 3.6% in 2011 and 5.1% in 2013. A623E mutation was not detected. The worrisome detection and the increase in the frequency of S769N and other mutations calls for urgent assessment of temporal changes of known artemisinin biomarkers in association within vivoACT efficacy. |
| Databáze: | OpenAIRE |
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