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Am J Trop Med Hyg ; 99(6): 1499-1503, 2018 12.
Artigo em Inglês | MEDLINE | ID: mdl-30350774

RESUMO

Drug-resistant Plasmodium falciparum is a major threat to global malaria control and elimination efforts. In Botswana, a southern African country approaching malaria elimination, P. falciparum molecular data are not available. Parasites were assessed through pollymerase chain reaction (PCR) for confirmation of positive rapid diagnostic tests, multiplicity of infection (MOI), and drug resistance markers among isolates from clinical uncomplicated malaria cases collected at health facilities. Of 211 dried blood spot samples selected for the study, 186 (88.2%) were PCR positive for P. falciparum. The mean MOI based on MSP1 genotyping was 2.3 and was not associated with age. A high prevalence of wild-type parasites for pfcrt and pfmdr1 was found, with a haplotype frequency (K76/N86) of 88.8% and 17.7% of the isolates having two copies of the pfmdr1 gene. For pfATPase6, all the parasites carried the wild-type S769 allele. Sequencing showed no evidence of non-synonymous mutations associated with reduced artemisinin derivative sensitivity in the P. falciparum k13 gene. In conclusion, we found that P. falciparum parasites in Botswana were mostly wild type for the drug resistance markers evaluated. Yet, there was a high rate of a molecular marker associated to reduced sensitivity to lumefantrine. Our results indicate the need for systematic drug efficacy surveillance to complement malaria elimination efforts.


Assuntos
ATPases Transportadoras de Cálcio/genética , Resistência a Medicamentos/genética , Malária Falciparum/epidemiologia , Proteínas de Membrana Transportadoras/genética , Proteínas Associadas à Resistência a Múltiplos Medicamentos/genética , Plasmodium falciparum/genética , Proteínas de Protozoários/genética , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Animais , Antimaláricos/uso terapêutico , Artemisininas/uso terapêutico , Botsuana/epidemiologia , Criança , Pré-Escolar , Monitoramento Epidemiológico , Feminino , Dosagem de Genes , Expressão Gênica , Marcadores Genéticos , Haplótipos , Humanos , Lactente , Lumefantrina/uso terapêutico , Malária Falciparum/tratamento farmacológico , Malária Falciparum/parasitologia , Masculino , Proteína 1 de Superfície de Merozoito/genética , Pessoa de Meia-Idade , Epidemiologia Molecular , Plasmodium falciparum/efeitos dos fármacos , Plasmodium falciparum/isolamento & purificação , Polimorfismo Genético
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