Mawili-Mboumba D P, Ndong Ngomo J M, Maboko F, Guiyedi V, Mourou Mbina J R, Kombila M, Bouyou Akotet M K
Department of Parasitology-Mycology, Faculty of Medicine, Université des Sciences de la Santé, Libreville, Gabon, BP 4009 Libreville, Gabon
Department of Parasitology-Mycology, Faculty of Medicine, Université des Sciences de la Santé, Libreville, Gabon, BP 4009 Libreville, Gabon.
Trans R Soc Trop Med Hyg. 2014 Nov;108(11):729-34. doi: 10.1093/trstmh/tru147. Epub 2014 Sep 23.
Studies showed that chloroquine resistance may revert to sensitivity after its withdrawal mainly detected by a significant decrease of Plasmodium falciparum pfcrt 76T and pfmdr1 86Y alleles. Besides, self-medication is considered as a key factor of antimalarial drug resistance expansion. Thus, pfcrt 76T and pfmdr1 86Y allele frequency and its relationship with antimalarial drug self-medication was analyzed in P. falciparum isolates collected in Gabon.
Samples were collected from febrile children screened for P. falciparum infection in 2005 and 2008 at the regional hospital of Oyem. Self-use of antimalarial drugs before the day of consultation was recorded. Polymorphic codons 76 and 86 of pfcrt and pfmdr1 genes were analyzed by PCR-RFLP.
The frequency of pfcrt 76T mutant allele was greater than 70.0% in 2005 and 2008. Wild type isolates were 1.7-fold more prevalent in 2008. The prevalence of pfmdr1 86Y mutant allele was comparable between 2005 and 2008 (p=0.1); the proportion of wild type allele reached 20.5% in 2008. The frequency of wild type allele pfcrt K76 or pfmdr1 N86 was higher among patients without anti-malarial drug self-medication compared to those who used it.
An increase of the frequency of P. falciparum wild type allele pfcrt 76K and pfmdr1 86N was observed within a short period after chloroquine withdrawal. The proportion of mutant genotypes is still high, mainly among patients using self-medication with antimalarial drugs.
研究表明,氯喹撤药后,疟原虫抗氯喹性可能恢复为敏感性,主要表现为恶性疟原虫pfcrt 76T和pfmdr1 86Y等位基因显著减少。此外,自我药疗被认为是抗疟药耐药性扩大的一个关键因素。因此,分析了加蓬采集的恶性疟原虫分离株中pfcrt 76T和pfmdr1 86Y等位基因频率及其与抗疟药自我药疗的关系。
样本采自2005年和2008年在奥耶姆地区医院筛查恶性疟原虫感染的发热儿童。记录就诊前一天抗疟药的自我使用情况。通过PCR-RFLP分析pfcrt和pfmdr1基因的多态密码子76和86。
2005年和2008年,pfcrt 76T突变等位基因频率大于70.0%。野生型分离株在2008年的流行率高1.7倍。2005年和2008年之间,pfmdr1 86Y突变等位基因的流行率相当(p=0.1);2008年野生型等位基因比例达到20.5%。与使用抗疟药自我药疗的患者相比,未进行自我药疗的患者中野生型等位基因pfcrt K76或pfmdr1 N86的频率更高。
氯喹撤药后短期内,观察到恶性疟原虫野生型等位基因pfcrt 76K和pfmdr1 86N频率增加。突变基因型比例仍然很高,主要在使用抗疟药自我药疗的患者中。