Bouyou-Akotet Marielle Karine, M'Bondoukwé Noé Patrick, Mawili-Mboumba Denise Patricia
Département de Parasitologie-Mycologie, Faculté de Médecine, Université des Sciences de la Santé, Libreville, Gabon - Unité de Recherche Clinique et Opérationnelle sur le Paludisme, Hôpital Régional de Melen, BP 4009, Libreville, Gabon.
Parasite. 2015;22:12. doi: 10.1051/parasite/2015012. Epub 2015 Mar 17.
We assessed Plasmodium (P.) falciparum allelic diversity based on clinical severity and age. The study was conducted from 2011 to 2012 in Libreville, Gabon where malaria prevalence was 24.5%. The polymorphism of the merozoite surface protein-1 (msp1) locus was analyzed in isolates from patients with complicated and uncomplicated malaria. Blood was collected on filter paper. After DNA extraction, genotyping of the msp1 gene was performed using nested PCR. The K1, Ro33, and Mad20 allelic families were detected in 71 (63%), 64 (57%), and 38 (34%) of the 112 analyzed samples, respectively. Overall, 17 K1 and 11 Mad20 alleles were detected. There was no association between msp1 allelic families and age. Mad20 allelic diversity increased with the severity of malaria. The number of K1 and Mad20 alleles decreased with age. The multiplicity of infection (MOI) was 1-6 genotypes and the complexity of infection (COI) 1.8 ± 1. The COI differed based on age: it was 1.9 (±1.1) in the isolates from adults, 1.8 (±1.1) in those from 0-5 year-old children, whereas it tended to be lower (1.6 ± 0.8) in those from 6-15 year-old children. Extensive genetic diversity is found in P. falciparum strains circulating in Libreville. The number of specific msp1 alleles increased with clinical severity, suggesting an association between the diversity and the severity of malaria.
我们基于临床严重程度和年龄评估了恶性疟原虫的等位基因多样性。该研究于2011年至2012年在加蓬利伯维尔进行,当地疟疾患病率为24.5%。对复杂型和非复杂型疟疾患者的分离株进行了裂殖子表面蛋白-1(msp1)基因座的多态性分析。血液采集在滤纸上。DNA提取后,使用巢式PCR对msp1基因进行基因分型。在112份分析样本中,分别有71份(63%)、64份(57%)和38份(34%)检测到K1、Ro33和Mad20等位基因家族。总体而言,检测到17个K1等位基因和11个Mad20等位基因。msp1等位基因家族与年龄之间无关联。Mad20等位基因多样性随疟疾严重程度增加。K1和Mad20等位基因数量随年龄减少。感染复数(MOI)为1 - 6种基因型,感染复杂性(COI)为1.8±1。COI因年龄而异:成人分离株中为1.9(±1.1),0 - 5岁儿童分离株中为1.8(±1.1),而6 - 15岁儿童分离株中往往较低(1.6±0.8)。在利伯维尔流行的恶性疟原虫菌株中发现了广泛的遗传多样性。特定msp1等位基因数量随临床严重程度增加,提示多样性与疟疾严重程度之间存在关联。