Cargando…

In Vitro Sensitivity of Plasmodium falciparum from China-Myanmar Border Area to Major ACT Drugs and Polymorphisms in Potential Target Genes

Drug resistance has always been one of the most important impediments to global malaria control. Artemisinin resistance has recently been confirmed in the Greater Mekong Subregion (GMS) and efforts for surveillance and containment are intensified. To determine potential mechanisms of artemisinin res...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Zenglei, Parker, Daniel, Meng, Hao, Wu, Lanou, Li, Jia, Zhao, Zhen, Zhang, Rongping, Fan, Qi, Wang, Haiyan, Cui, Liwang, Yang, Zhaoqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3365119/
https://www.ncbi.nlm.nih.gov/pubmed/22701513
http://dx.doi.org/10.1371/journal.pone.0030927
_version_ 1782234645528576000
author Wang, Zenglei
Parker, Daniel
Meng, Hao
Wu, Lanou
Li, Jia
Zhao, Zhen
Zhang, Rongping
Fan, Qi
Wang, Haiyan
Cui, Liwang
Yang, Zhaoqing
author_facet Wang, Zenglei
Parker, Daniel
Meng, Hao
Wu, Lanou
Li, Jia
Zhao, Zhen
Zhang, Rongping
Fan, Qi
Wang, Haiyan
Cui, Liwang
Yang, Zhaoqing
author_sort Wang, Zenglei
collection PubMed
description Drug resistance has always been one of the most important impediments to global malaria control. Artemisinin resistance has recently been confirmed in the Greater Mekong Subregion (GMS) and efforts for surveillance and containment are intensified. To determine potential mechanisms of artemisinin resistance and monitor the emergence and spread of resistance in other regions of the GMS, we investigated the in vitro sensitivity of 51 culture-adapted parasite isolates from the China-Myanmar border area to four drugs. The 50% inhibitory concentrations (IC(50)s) of dihydroartemisinin, mefloquine and lumefantrine were clustered in a relatively narrow, 3- to 6-fold range, whereas the IC(50) range of artesunate was 12-fold. We assessed the polymorphisms of candidate resistance genes pfcrt, pfmdr1, pfATP6, pfmdr6 and pfMT (a putative metabolite/drug transporter). The K76T mutation in pfcrt reached fixation in the study parasite population, whereas point mutations in pfmdr1 and pfATP6 had low levels of prevalence. In addition, pfmdr1 gene amplification was not detected. None of the mutations in pfmdr1 and pfATP6 was associated significantly with in vitro sensitivity to artemisinin derivatives. The ABC transporter gene pfmdr6 harbored two point mutations, two indels, and number variations in three simple repeats. Only the length variation in a microsatellite repeat appeared associated with altered sensitivity to dihydroartemisinin. The PfMT gene had two point mutations and one codon deletion; the I30N and N496– both reached high levels of prevalence. However, none of the SNPs or haplotypes in PfMT were correlated significantly with resistance to the four tested drugs. Compared with other parasite populations from the GMS, our studies revealed drastically different genotype and drug sensitivity profiles in parasites from the China-Myanmar border area, where artemisinins have been deployed extensively for over 30 years.
format Online
Article
Text
id pubmed-3365119
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-33651192012-06-14 In Vitro Sensitivity of Plasmodium falciparum from China-Myanmar Border Area to Major ACT Drugs and Polymorphisms in Potential Target Genes Wang, Zenglei Parker, Daniel Meng, Hao Wu, Lanou Li, Jia Zhao, Zhen Zhang, Rongping Fan, Qi Wang, Haiyan Cui, Liwang Yang, Zhaoqing PLoS One Research Article Drug resistance has always been one of the most important impediments to global malaria control. Artemisinin resistance has recently been confirmed in the Greater Mekong Subregion (GMS) and efforts for surveillance and containment are intensified. To determine potential mechanisms of artemisinin resistance and monitor the emergence and spread of resistance in other regions of the GMS, we investigated the in vitro sensitivity of 51 culture-adapted parasite isolates from the China-Myanmar border area to four drugs. The 50% inhibitory concentrations (IC(50)s) of dihydroartemisinin, mefloquine and lumefantrine were clustered in a relatively narrow, 3- to 6-fold range, whereas the IC(50) range of artesunate was 12-fold. We assessed the polymorphisms of candidate resistance genes pfcrt, pfmdr1, pfATP6, pfmdr6 and pfMT (a putative metabolite/drug transporter). The K76T mutation in pfcrt reached fixation in the study parasite population, whereas point mutations in pfmdr1 and pfATP6 had low levels of prevalence. In addition, pfmdr1 gene amplification was not detected. None of the mutations in pfmdr1 and pfATP6 was associated significantly with in vitro sensitivity to artemisinin derivatives. The ABC transporter gene pfmdr6 harbored two point mutations, two indels, and number variations in three simple repeats. Only the length variation in a microsatellite repeat appeared associated with altered sensitivity to dihydroartemisinin. The PfMT gene had two point mutations and one codon deletion; the I30N and N496– both reached high levels of prevalence. However, none of the SNPs or haplotypes in PfMT were correlated significantly with resistance to the four tested drugs. Compared with other parasite populations from the GMS, our studies revealed drastically different genotype and drug sensitivity profiles in parasites from the China-Myanmar border area, where artemisinins have been deployed extensively for over 30 years. Public Library of Science 2012-05-31 /pmc/articles/PMC3365119/ /pubmed/22701513 http://dx.doi.org/10.1371/journal.pone.0030927 Text en Wang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wang, Zenglei
Parker, Daniel
Meng, Hao
Wu, Lanou
Li, Jia
Zhao, Zhen
Zhang, Rongping
Fan, Qi
Wang, Haiyan
Cui, Liwang
Yang, Zhaoqing
In Vitro Sensitivity of Plasmodium falciparum from China-Myanmar Border Area to Major ACT Drugs and Polymorphisms in Potential Target Genes
title In Vitro Sensitivity of Plasmodium falciparum from China-Myanmar Border Area to Major ACT Drugs and Polymorphisms in Potential Target Genes
title_full In Vitro Sensitivity of Plasmodium falciparum from China-Myanmar Border Area to Major ACT Drugs and Polymorphisms in Potential Target Genes
title_fullStr In Vitro Sensitivity of Plasmodium falciparum from China-Myanmar Border Area to Major ACT Drugs and Polymorphisms in Potential Target Genes
title_full_unstemmed In Vitro Sensitivity of Plasmodium falciparum from China-Myanmar Border Area to Major ACT Drugs and Polymorphisms in Potential Target Genes
title_short In Vitro Sensitivity of Plasmodium falciparum from China-Myanmar Border Area to Major ACT Drugs and Polymorphisms in Potential Target Genes
title_sort in vitro sensitivity of plasmodium falciparum from china-myanmar border area to major act drugs and polymorphisms in potential target genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3365119/
https://www.ncbi.nlm.nih.gov/pubmed/22701513
http://dx.doi.org/10.1371/journal.pone.0030927
work_keys_str_mv AT wangzenglei invitrosensitivityofplasmodiumfalciparumfromchinamyanmarborderareatomajoractdrugsandpolymorphismsinpotentialtargetgenes
AT parkerdaniel invitrosensitivityofplasmodiumfalciparumfromchinamyanmarborderareatomajoractdrugsandpolymorphismsinpotentialtargetgenes
AT menghao invitrosensitivityofplasmodiumfalciparumfromchinamyanmarborderareatomajoractdrugsandpolymorphismsinpotentialtargetgenes
AT wulanou invitrosensitivityofplasmodiumfalciparumfromchinamyanmarborderareatomajoractdrugsandpolymorphismsinpotentialtargetgenes
AT lijia invitrosensitivityofplasmodiumfalciparumfromchinamyanmarborderareatomajoractdrugsandpolymorphismsinpotentialtargetgenes
AT zhaozhen invitrosensitivityofplasmodiumfalciparumfromchinamyanmarborderareatomajoractdrugsandpolymorphismsinpotentialtargetgenes
AT zhangrongping invitrosensitivityofplasmodiumfalciparumfromchinamyanmarborderareatomajoractdrugsandpolymorphismsinpotentialtargetgenes
AT fanqi invitrosensitivityofplasmodiumfalciparumfromchinamyanmarborderareatomajoractdrugsandpolymorphismsinpotentialtargetgenes
AT wanghaiyan invitrosensitivityofplasmodiumfalciparumfromchinamyanmarborderareatomajoractdrugsandpolymorphismsinpotentialtargetgenes
AT cuiliwang invitrosensitivityofplasmodiumfalciparumfromchinamyanmarborderareatomajoractdrugsandpolymorphismsinpotentialtargetgenes
AT yangzhaoqing invitrosensitivityofplasmodiumfalciparumfromchinamyanmarborderareatomajoractdrugsandpolymorphismsinpotentialtargetgenes