Ogouyèmi-Hounto Aurore, Gazard Dorothée Kinde, Ndam Nicaise, Topanou Elsa, Garba Olivia, Elegbe Pancras, Hountohotegbe Tatiana, Massougbodji Achille
Unité d'Enseignement et de Recherche en Parasitologie-Mycologie de la Faculté des Sciences de la Santé, 01BP188 Cotonou, Bénin - Laboratoire du Centre de Lutte Intégrée contre le Paludisme, 01BP188 Cotonou, Bénin.
Parasite. 2013;20:37. doi: 10.1051/parasite/2013039. Epub 2013 Oct 21.
The aim of this study was to determine the genetic diversity of Plasmodium falciparum by analyzing the polymorphism of the msp-1 and msp-2 genes and the multiplicity of infection in children with uncomplicated malaria in southern Benin. Blood samples of children with fever or history of fever with thick smear positive P. falciparum were collected on filter paper. After extraction of DNA by Chelex®, the samples underwent nested PCR. 93 isolates from children were genotyped. For the msp-1 gene, the K1 and R033 sequences were the most represented in the study population with 85.2% and 83% prevalence, respectively. Regarding the msp-2 gene, the FC27 family was more highly represented with 99% prevalence against 81.5% for 3D7. Mixed infections accounted for 80.4% of the samples. Twenty-five alleles were identified for msp-1 and 28 for msp-2. Fourteen and ten alleles belonged to the K1 (100-500 bp) and MAD20 (100-500 bp) families, respectively. The RO33 sequence did not show any polymorphism, with only one variant (160 bp) detected. The msp-2 gene was present as 16 FC27 family fragments (250-800 bp) and 12 of the 3D7 family (350-700 bp). The multiplicity of infection was estimated at 3.8 for msp-1 and 3.9 for msp-2 with 77 (87.5%) and 84 (91.3%) samples harboring more than one parasite genotype for msp-1 and msp-2, respectively. The multiplicity of infection (MOI) was influenced neither by age nor by parasite density. This study shows a significant diversity of P. falciparum in southern Benin with an MOI unaffected by age or by parasite density.
本研究的目的是通过分析贝宁南部单纯性疟疾患儿中恶性疟原虫的msp-1和msp-2基因多态性及感染复数,来确定恶性疟原虫的遗传多样性。采集滤纸滤纸上发热或有发热史且厚涂片疟原虫阳性的患儿血样。用Chelex®提取DNA后,样本进行巢式PCR。对93例患儿的分离株进行基因分型。对于msp-1基因,K1和R033序列在研究人群中占比最高,流行率分别为85.2%和83%。对于msp-2基因,FC27家族占比更高,流行率为99%,而3D7为81.5%。混合感染占样本的80.4%。msp-1鉴定出25个等位基因,msp-2鉴定出28个等位基因。分别有14个和10个等位基因属于K1(100 - 500 bp)和MAD20(100 - 500 bp)家族。RO33序列未显示任何多态性,仅检测到一个变体(160 bp)。msp-2基因以16个FC27家族片段(250 - 800 bp)和3D7家族的12个片段(350 - 700 bp)形式存在。msp-1的感染复数估计为3.8,msp-2为3.9,分别有77例(87.5%)和84例(91.3%)样本携带一种以上msp-1和msp-2寄生虫基因型。感染复数(MOI)不受年龄和寄生虫密度影响。本研究表明,贝宁南部恶性疟原虫具有显著的多样性,且MOI不受年龄或寄生虫密度的影响。