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东马来西亚沙巴州疟疾流行下降地区恶性疟原虫种群的遗传多样性

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

作者信息

Mohd Abd Razak Mohd Ridzuan, Sastu Umi Rubiah, Norahmad Nor Azrina, Abdul-Karim Abass, Muhammad Amirrudin, Muniandy Prem Kumar, Jelip Jenarun, Rundi Christina, Imwong Mallika, Mudin Rose Nani, Abdullah Noor Rain

机构信息

Herbal Medicine Research Center, Institute for Medical Research, Kuala Lumpur, Malaysia.

Zonal Public Health Laboratory, Tamale Teaching Hospital, Tamale, Northern Region, Ghana, West Africa.

出版信息

PLoS One. 2016 Mar 29;11(3):e0152415. doi: 10.1371/journal.pone.0152415. eCollection 2016.

Abstract

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.

摘要

马来西亚有一个到2020年消除疟疾的国家目标。了解残余传播疫源地疟原虫的遗传多样性可以提供宝贵信息,这可能为实现消除目标所采用的干预策略提供依据。本研究旨在确定沙巴州疟疾残余疫源地地区恶性疟原虫分离株的遗传多样性水平。在卡拉巴干和哥打马鲁都开展了疟疾主动病例检测。通过快速诊断检测对研究地点的所有个体进行疟疾感染筛查。在提取DNA之前,从感染恶性疟原虫的个体采集滤纸血样。使用裂殖子表面蛋白-1(MSP-1)、裂殖子表面蛋白-2(MSP-2)、富含谷氨酸蛋白(GLURP)和10个中性微卫星位点标记进行基因分型。确定了等位基因大小、感染复数(MOI)、等位基因平均数(Na)、期望杂合度(He)、连锁不平衡(LD)和遗传分化(FST)。在卡拉巴干,MSP-1和MSP-2等位基因分别主要为K1和FC27家族类型。GLURP基因型VI(751 - 800 bp)占主导。MSP-1和MSP-2的MOI分别为1.65和1.20。每个微卫星位点的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。在哥打马鲁都,MSP-1和MSP-2等位基因分别主要为MAD20和3D7家族类型。GLURP基因型IV(651 - 700 bp)占主导。MSP-1和MSP-2的MOI均为1.05。每个微卫星位点的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。在卡拉巴干(0.495,p<0.01)和哥打马鲁都恶性疟原虫种群(0.601,p<0.01)中观察到显著的LD。观察到卡拉巴干和哥打马鲁都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沙巴州疟疾流行下降地区恶性疟原虫种群的有限多样性和对比鲜明的遗传模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca69/4811561/30dd5d42c841/pone.0152415.g001.jpg

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