| Literature DB >> 27430541 |
Lindsay Carol Morton1, Curtis Huber1, Sheila Akinyi Okoth2, Sean Griffing1, Naomi Lucchi1, Dragan Ljolje2, Jacques Boncy3, Roland Oscar4, David Townes1, Meredith McMorrow1, Michelle A Chang1, Venkatachalam Udhayakumar1, John W Barnwell5.
Abstract
Chloroquine (CQ) remains the first-line treatment of malaria in Haiti. Given the challenges of conducting in vivo drug efficacy trials in low-endemic settings like Haiti, molecular surveillance for drug resistance markers is a reasonable approach for detecting resistant parasites. In this study, 349 blood spots were collected from suspected malaria cases in areas in and around Port-au-Prince from March to July 2010. Among them, 121 samples that were Plasmodium falciparum positive by polymerase chain reaction were genotyped for drug-resistant pfcrt, pfdhfr, pfdhps, and pfmdr1 alleles. Among the 108 samples that were successfully sequenced for CQ resistant markers in pfcrt, 107 were wild type (CVMNK), whereas one sample carried a CQ-resistant allele (CVIET). Neutral microsatellite genotyping revealed that the CQ-resistant isolate was distinct from all other samples in this study. Furthermore, the remaining parasite specimens appeared to be genetically distinct from other reported Central and South American populations. © The American Society of Tropical Medicine and Hygiene.Entities:
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Year: 2016 PMID: 27430541 PMCID: PMC5062779 DOI: 10.4269/ajtmh.16-0214
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 2.345