| Autor: |
Wirjanata, Grennady, Handayuni, Irene, Prayoga, Pak, Leonardo, Leo, Apriyanti, Dwi, Trianty, Leily, Wandosa, Ruland, Gobay, Basbak, Kenangalem, Enny, Poespoprodjo, Jeanne Rini, Noviyanti, Rintis, Kyle, Dennis E., Cheng, Qin, Price, Ric N., Marfurt, Jutta |
| Zdroj: |
Antimicrobial Agents and Chemotherapy; May 2017, Vol. 61 Issue: 8 |
| Abstrakt: |
ABSTRACTHigh-grade chloroquine (CQ) resistance has emerged in both Plasmodium falciparumand P. vivax. The aim of the present study was to investigate the phenotypic differences of CQ resistance in both of these species and the ability of known CQ resistance reversal agents (CQRRAs) to alter CQ susceptibility. Between April 2015 and April 2016, the potential of verapamil (VP), mibefradil (MF), L703,606 (L7), and primaquine (PQ) to reverse CQ resistance was assessed in 46 P. falciparumand 34 P. vivaxclinical isolates in Papua, Indonesia, where CQ resistance is present in both species, using a modified schizont maturation assay. In P. falciparum, CQ 50% inhibitory concentrations (IC50s) were reduced when CQ was combined with VP (1.4-fold), MF (1.2-fold), L7 (4.2-fold), or PQ (1.8-fold). The degree of CQ resistance reversal in P. falciparumwas highly correlated with CQ susceptibility for all CQRRAs (R2= 0.951, 0.852, 0.962, and 0.901 for VP, MF, L7, and PQ, respectively), in line with observations in P. falciparumlaboratory strains. In contrast, no reduction in the CQ IC50s was observed with any of the CQRRAs in P. vivax, even in those isolates with high chloroquine IC50s. The differential effect of CQRRAs in P. falciparumand P. vivaxsuggests significant differences in CQ kinetics and, potentially, the likely mechanism of CQ resistance between these two species. |
| Databáze: |
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