1. Longitudinal surveillance of drug resistance in Plasmodium falciparum isolates from the China-Myanmar border reveals persistent circulation of multidrug resistant parasites.
- Author
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Bai Y, Zhang J, Geng J, Xu S, Deng S, Zeng W, Wang Z, Ngassa Mbenda HG, Zhang J, Li N, Wu Y, Li C, Liu H, Ruan Y, Cao Y, Yang Z, and Cui L
- Subjects
- Artemisinins pharmacology, China epidemiology, Chloroquine pharmacology, Epidemiological Monitoring, Genotype, Humans, In Vitro Techniques, Inhibitory Concentration 50, Lumefantrine pharmacology, Malaria, Falciparum parasitology, Multidrug Resistance-Associated Proteins genetics, Mutation, Myanmar epidemiology, Protozoan Proteins genetics, Antimalarials pharmacology, Drug Resistance, Multiple, Malaria, Falciparum epidemiology, Plasmodium falciparum drug effects, Plasmodium falciparum genetics
- Abstract
Multidrug-resistant Plasmodium falciparum in the Greater Mekong Subregion of Southeast Asia is a major threat to malaria elimination and requires close surveillance. In this study, we collected 107 longitudinal clinical samples of P. falciparum in 2007-2012 from the malaria hypoendemic region of the China-Myanmar border and measured their in vitro susceptibilities to 10 antimalarial drugs. Overall, parasites had significantly different IC
50 values to all the drugs tested as compared to the reference 3D7 strain. Parasites were also genotyped in seven genes that were associated with drug resistance including pfcrt, pfmdr1, pfmrp1, pfdhfr, pfdhps, pfnhe1, and PfK13 genes. Despite withdrawal of chloroquine and antifolates from treating P. falciparum, parasites remained highly resistant to these drugs and mutations in pfcrt, pfdhfr, and pfdhps genes were highly prevalent and almost reached fixation in the study parasite population. Except for pyronaridine, quinine and lumefantrine, all other tested drugs exhibited significant temporal variations at least between some years, but only chloroquine and piperaquine had a clear temporal trend of continuous increase of IC50 s. For the pfmrp1 gene, several mutations were associated with altered sensitivity to a number of drugs tested including chloroquine, piperaquine, lumefantrine and dihydroartemisinin. The association of PfK13 mutations with resistance to multiple drugs suggests potential evolution of PfK13 mutations amid multidrug resistance genetic background. Furthermore, network analysis of drug resistance genes indicated that certain haplotypes associated multidrug resistance persisted in these years, albeit there were year-to-year fluctuations of the predominant haplotypes., (Copyright © 2018. Published by Elsevier Ltd.)- Published
- 2018
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