dc.creatorCosta, Gabriel Luíz
dc.creatorAmaral, Lara Cotta
dc.creatorFontes, Cor Jesus Fernandes
dc.creatorCarvalho, Luzia Helena de
dc.creatorBrito, Cristiana Ferreira Alves de
dc.creatorSousa, Taís Nóbrega de
dc.date2018-03-23T18:13:08Z
dc.date2018-03-23T18:13:08Z
dc.date2017
dc.date.accessioned2023-09-26T20:57:23Z
dc.date.available2023-09-26T20:57:23Z
dc.identifierCOSTA, Gabriel Luíz et al. Assessment of copy number variation in genes related to drug resistance in Plasmodium vivax and Plasmodium falciparum isolates from the Brazilian Amazon and a systematic review of the literature. Malaria Journal, v. 16, art. 152, 2017
dc.identifier1475-2875
dc.identifierhttps://www.arca.fiocruz.br/handle/icict/25477
dc.identifier10.1186/s12936-017-1806-z
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8866785
dc.descriptionBackground: Parasite resistance to anti-malarials represents a great obstacle for malaria elimination. The majority of studies have investigated the association between single-nucleotide polymorphisms (SNPs) and drug resistance; however, it is becoming clear that the copy number variation (CNV) is also associated with this parasite phenotype. To provide a baseline for molecular surveillance of anti-malarial drug resistance in the Brazilian Amazon, the present study characterized the genetic profile of both markers in the most common genes associated with drug resistance in Plasmodium falciparum and Plasmodium vivax isolates. Additionally, these data were compared to data published elsewhere applying a systematic review of the literature published over a 20-year time period. Methods: The genomic DNA of 67 patients infected by P. falciparum and P. vivax from three Brazilian States was obtained between 2002 and 2012. CNV in P. falciparum multidrug resistance gene-1 (pfmdr1), GTP cyclohydrolase 1 (pfgch1) and P. vivax multidrug resistance gene-1 (pvmdr1) were assessed by real-time PCR assays. SNPs in the pfmdr1 and pfcrt genes were assessed by PCR–RFLP. A literature search for studies that analysed CNP in the same genes of P. falciparum and P. vivax was conducted between May 2014 and March 2017 across four databases. Results: All analysed samples of P. falciparum carried only one copy of pfmdr1 or pfgch1. Although the pfcrt K76T polymorphism, a determinant of CQ resistance, was present in all samples genotyped, the pfmdr1 N86Y was absent. For P. vivax isolates, an amplification rate of 20% was found for the pvmdr1 gene. The results of the study are in agreement with the low amplification rates for pfmdr1 gene evidenced in the Americas and Africa, while higher rates have been described in Southeast Asia. For P. vivax, very low rates of amplification for pvmdr1 have been described worldwide, with exceptions in French Guiana, Cambodia, Thailand and Brazil. Conclusions: The present study was the first to evaluate gch1 CNV in P. falciparum isolates from Brazil, showing an absence of amplification of this gene more than 20 years after the withdrawal of the Brazilian antifolates therapeutic scheme. Furthermore, the rate of pvmdr1 amplification was significantly higher than that previously reported for isolates circulating in Northern Brazil.
dc.description2020-01-01
dc.formatapplication/pdf
dc.languageeng
dc.publisherBiomed Central
dc.rightsopen access
dc.subjectMalaria
dc.subjectPlasmodium falciparum
dc.subjectPlasmodium vivax
dc.subjectresistencia a drogas
dc.subjectMalaria
dc.subjectPlasmodium falciparum
dc.subjectPlasmodium vivax
dc.subjectDrug resistance
dc.titleAssessment of copy number variation in genes related to drug resistance in Plasmodium vivax and Plasmodium falciparum isolates from the Brazilian Amazon and a systematic review of the literature
dc.typeArticle


Este ítem pertenece a la siguiente institución