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Genetic Diversity of Plasmodium falciparum Populations in Malaria Declining Areas of Sabah East Malaysia

机译:东马来西亚沙巴州疟疾衰退地区恶性疟原虫种群的遗传多样性

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摘要

Malaysia has a national goal to eliminate malaria by 2020. Understanding the genetic diversity of malaria parasites in residual transmission foci can provide invaluable information which may inform the intervention strategies used to reach elimination targets. This study was conducted to determine the genetic diversity level of P. falciparum isolates in malaria residual foci areas of Sabah. Malaria active case detection was conducted in Kalabakan and Kota Marudu. All individuals in the study sites were screened for malaria infection by rapid diagnostic test. Blood from P. falciparum-infected individuals were collected on filter paper prior to DNA extraction. Genotyping was performed using merozoite surface protein-1 (MSP-1), merozoite surface protein-2 (MSP-2), glutamate rich protein (GLURP) and 10 neutral microsatellite loci markers. The size of alleles, multiplicity of infection (MOI), mean number of alleles (Na), expected heterozygosity (He), linkage disequilibrium (LD) and genetic differentiation (FST) were determined. In Kalabakan, the MSP-1 and MSP-2 alleles were predominantly K1 and FC27 family types, respectively. The GLURP genotype VI (751–800 bp) was predominant. The MOI for MSP-1 and MSP-2 were 1.65 and 1.20, respectively. The Na per microsatellite locus was 1.70. The He values for MSP-1, MSP-2, GLURP and neutral microsatellites were 0.17, 0.37, 0.70 and 0.33, respectively. In Kota Marudu, the MSP-1 and MSP-2 alleles were predominantly MAD20 and 3D7 family types, respectively. The GLURP genotype IV (651–700 bp) was predominant. The MOI for both MSP-1 and MSP-2 was 1.05. The Na per microsatellite locus was 3.60. The He values for MSP-1, MSP-2, GLURP and neutral microsatellites were 0.24, 0.25, 0.69 and 0.30, respectively. A significant LD was observed in Kalabakan (0.495, p<0.01) and Kota Marudu P. falciparum populations (0.601, p<0.01). High genetic differentiation between Kalabakan and Kota Marudu P. falciparum populations was observed (FST = 0.532). The genetic data from the present study highlighted the limited diversity and contrasting genetic pattern of P. falciparum populations in the malaria declining areas of Sabah.
机译:马来西亚的国家目标是到2020年消除疟疾。了解残留传播疫源地疟疾寄生虫的遗传多样性可以提供宝贵的信息,这些信息可以为实现消除目标的干预策略提供信息。这项研究是为了确定沙巴州疟疾残留疫源地恶性疟原虫分离株的遗传多样性水平。在卡拉巴坎和哥打玛鲁都进行了疟疾活跃病例检测。通过快速诊断测试,对研究地点的所有个体进行了疟疾感染筛查。在提取DNA之前,将恶性疟原虫感染者的血液收集在滤纸上。使用裂殖子表面蛋白-1(MSP-1),裂殖子表面蛋白-2(MSP-2),富含谷氨酸的蛋白(GLURP)和10个中性微卫星基因座标记进行基因分型。确定了等位基因的大小,感染复数(MOI),平均等位基因数(Na),预期杂合性(He),连锁不平衡(LD)和遗传分化(FST)。在卡拉巴坎,MSP-1和MSP-2等位基因分别主要是K1和FC27家族类型。 GLURP基因型VI(751-800 bp)占优势。 MSP-1和MSP-2的MOI分别为1.65和1.20。每个微卫星基因座的Na为1.70。 MSP-1,MSP-2,GLURP和中性微卫星的He值分别为0.17、0.37、0.70和0.33。在亚庇(Kota Marudu),MSP-1和MSP-2等位基因分别主要是MAD20和3D7家族类型。 GLURP基因型为IV(651–700 bp)。 MSP-1和MSP-2的MOI均为1.05。每个微卫星基因座的Na为3.60。 MSP-1,MSP-2,GLURP和中性微卫星的He值分别为0.24、0.25、0.69和0.30。在Kalabakan(0.495,p <0.01)和Kota Marudu恶性疟原虫种群(0.601,p <0.01)中观察到了显着的LD。观察到Kalabakan和Kota Marudu恶性疟原虫种群之间存在高度遗传分化(FST = 0.532)。本研究的遗传数据突出了 P 的有限多样性和相反的遗传模式。沙巴疟疾下降地区的 falciparum 种群。

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