Duah Nancy O, Matrevi Sena A, Quashie Neils B, Abuaku Benjamin, Koram Kwadwo A
Epidemiology Department, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, P. O. Box LG581, Legon, Ghana.
Centre for Tropical Clinical Pharmacology and Therapeutics, School of Medicine and Dentistry, College of Health Sciences, University of Ghana, P. O. Box GP 4260, Accra, Ghana.
Parasit Vectors. 2016 Jul 26;9(1):416. doi: 10.1186/s13071-016-1692-1.
Genotyping malaria parasites to assess their diversity in different geographic settings have become necessary for the selection of antigenic epitopes for vaccine development and for antimalarial drug efficacy or resistance investigations. This study describes the genetic diversity of Plasmodium falciparum isolates from uncomplicated malaria cases over a ten year period (2003-2013) in Ghana using the polymorphic antigenic marker, merozoite surface protein 2 (msp2).
Archived filter paper blood blots from children aged nine years and below with uncomplicated malaria collected from nine sites in Ghana were typed for the presence of the markers. A total of 880 samples were genotyped for msp2 for the two major allelic families, FC27 and 3D7, using nested polymerase chain reaction (PCR). The allele frequencies and the multiplicity of infection were determined for the nine sites for five time points over a period of ten years, 2003-2004, 2005-2006, 2007-2008, 2010 and 2012-2013 malaria transmission seasons.
The number of different alleles detected for the msp2 gene by resolving PCR products on agarose gels was 14. Both of the major allelic families, 3D7 and FC27 were common in all population samples. The highest multiplicity of infection (MOI) was observed in isolates from Begoro (forest zone, rural site): 3.31 for the time point 2007-2008. A significant variation was observed among the sites in the MOIs detected per infection (Fisher's exact test, P < 0.001) for the 2007 isolates and also at each of the three sites with data for three different years, Hohoe, P = 0.03; Navrongo, P < 0.001; Cape Coast, P < 0.001. Overall, there was no significant difference between the MOIs of the three ecological zones over the years (P = 0.37) and between the time points when data from all sites were pooled (P = 0.40).
The diversity and variation between isolates detected using the msp2 gene in Ghanaian isolates were observed to be profound; however, there was homogeneity throughout the three ecological zones studied. This is indicative of gene flow between the parasite populations across the country probably due to human population movements (HPM).
对疟原虫进行基因分型以评估其在不同地理环境中的多样性,对于疫苗开发中抗原表位的选择以及抗疟药物疗效或耐药性研究而言已变得十分必要。本研究利用多态性抗原标记物裂殖子表面蛋白2(msp2),描述了加纳在十年期间(2003 - 2013年)非重症疟疾病例中恶性疟原虫分离株的遗传多样性。
对从加纳九个地点收集的9岁及以下患非重症疟疾儿童的存档滤纸血斑进行标记物检测。使用巢式聚合酶链反应(PCR)对总共880个样本的msp2两个主要等位基因家族FC27和3D7进行基因分型。在2003 - 2004年、2005 - 2006年、2007 - 2008年、2010年以及2012 - 2013年疟疾传播季节的五个时间点,确定了九个地点的等位基因频率和感染复数。
通过在琼脂糖凝胶上解析PCR产物检测到的msp2基因不同等位基因数量为14个。两个主要等位基因家族3D7和FC27在所有群体样本中都很常见。在来自贝戈罗(森林地带,农村地点)的分离株中观察到最高感染复数(MOI):在2007 - 2008时间点为3.31。对于2007年的分离株以及有三年不同数据的三个地点(霍霍埃,P = 0.03;纳夫龙戈,P < 0.001;海岸角,P < 0.001)中的每一个地点,在每次感染中检测到的MOI之间观察到显著差异(Fisher精确检验,P < 0.001)。总体而言,多年来三个生态区的MOI之间(P = 0.37)以及汇总所有地点数据的时间点之间(P = 0.40)没有显著差异。
观察到加纳分离株中使用msp2基因检测到的分离株之间的多样性和变异很显著;然而,在所研究的三个生态区中存在同质性。这表明全国范围内寄生虫群体之间可能由于人口流动(HPM)而存在基因流动。