Malaria, Neglected Tropical Diseases Research Team Bacterial, Parasitic, Zoonotic Diseases Research Directorate, Ethiopian Public Health Institute, Addis Ababa, Ethiopia.
Menzies School of Health Research and Charles Darwin University, Darwin, Australia.
Malar J. 2018 Oct 25;17(1):386. doi: 10.1186/s12936-018-2540-x.
Determination of the genetic diversity of malaria parasites can inform the intensity of transmission and identify potential deficiencies in malaria control programmes. This study was conducted to characterize the genetic diversity and allele frequencies of Plasmodium falciparum in Northwest Ethiopia along the Eritrea and Sudan border.
A total of 90 isolates from patients presenting to the local health centre with uncomplicated P. falciparum were collected from October 2014 to January 2015. DNA was extracted and the polymorphic regions of the msp-1, msp-2 and glurp loci were genotyped by nested polymerase chain reactions followed by gel electrophoresis for fragment analysis.
Allelic variation in msp-1, msp-2 and glurp were identified in 90 blood samples. A total of 34 msp alleles (12 for msp-1 and 22 for msp-2) were detected. For msp-1 97.8% (88/90), msp-2 82.2% (74/90) and glurp 46.7% (42/90) were detected. In msp-1, MAD20 was the predominant allelic family detected in 47.7% (42/88) of the isolates followed by RO33 and K1. For msp-2, the frequency of FC27 and IC/3D7 were 77% (57/74) and 76% (56/74), respectively. Nine glurp RII region genotypes were identified. Seventy percent of isolates had multiple genotypes and the overall mean multiplicity of infection was 2.6 (95% CI 2.25-2.97). The heterozygosity index was 0.82, 0.62 and 0.20 for msp-1, msp-2 and glurp, respectively. There was no significant association between multiplicity of infection and age or parasite density.
There was a high degree of genetic diversity with multiple clones in P. falciparum isolates from Northwest Ethiopia suggesting that there is a need for improved malaria control efforts in this region.
疟疾寄生虫的遗传多样性的确定可以提供传播强度的信息,并发现疟疾控制规划的潜在缺陷。本研究旨在描述埃塞俄比亚西北部与厄立特里亚和苏丹接壤地区恶性疟原虫的遗传多样性和等位基因频率。
从 2014 年 10 月至 2015 年 1 月,从当地卫生中心就诊的患有无并发症恶性疟原虫的患者中采集了 90 株分离株。提取 DNA 后,通过巢式聚合酶链反应对 msp-1、msp-2 和 glurp 基因座的多态性区域进行基因分型,然后进行凝胶电泳进行片段分析。
在 90 份血样中鉴定出 msp-1、msp-2 和 glurp 的等位基因变异。共检测到 34 个 msp 等位基因(msp-1 为 12 个,msp-2 为 22 个)。msp-1 的阳性率为 97.8%(88/90),msp-2 的阳性率为 82.2%(74/90),glurp 的阳性率为 46.7%(42/90)。在 msp-1 中,检测到的主要等位基因家族 MAD20 占分离株的 47.7%(42/88),其次是 RO33 和 K1。在 msp-2 中,FC27 和 IC/3D7 的频率分别为 77%(57/74)和 76%(56/74)。鉴定出 9 种 glurp RII 区基因型。70%的分离株具有多种基因型,总感染多重性为 2.6(95%CI 2.25-2.97)。msp-1、msp-2 和 glurp 的杂合度指数分别为 0.82、0.62 和 0.20。感染多重性与年龄或寄生虫密度之间无显著相关性。
来自埃塞俄比亚西北部的恶性疟原虫分离株具有高度的遗传多样性和多个克隆,表明该地区需要加强疟疾控制工作。