Soulama I, Sawadogo M, Nebie I, Diarra A, Tiono A B, Konate A, Sirima S B
Centre national de recherche et de formation sur le paludisme, Ministère de la santé, 01 BP 2208 Ouagadougou 01, Burkina Faso.
Bull Soc Pathol Exot. 2006 Jul;99(3):166-70.
The clinical presentation of malaria mainly the severe form may be related to Plasmodium falciparum msp-2 (merozoite surface protein 2) specific family To verify this hypothesis, during the high malaria transmission season in 2001; we analyzed the allelic polymorphism of the msp-2 gene of P. falciparum in children under 5 years old with different presentation of malaria in the regional Hospital and at community level in the Boulgou Province (Burkina Faso). A total of 405 children (107 severe malarial anaemia cases, 102 severe malaria cases without severe anaemia and 196 non severe malaria cases) were enrolled in the study. The frequencies of the FC27 were 89.2% in severe malarial anaemia children group, then 89.7% and 86.9% respectively in severe malaria non anaemic children cases and non severe malaria cases (P = 0.4). The frequencies of the 3D7 were 72.5%; 84.1% and 77% respectively severe malaria non anaemic children, severe malarial anaemia cases and non severe malaria cases (P = 0.7). The complexity of the FC27 genotypes was significantly higher in children with severe malaria (with and without severe anaemia) compared to the non severe malarial children (P << 0.001). No significant difference was pointed up in the complexity of the 3D7 genotypes.
疟疾的临床表现,主要是严重形式,可能与恶性疟原虫的裂殖子表面蛋白2(msp-2)特定家族有关。为验证这一假设,在2001年疟疾高传播季节,我们在布基纳法索布尔古省的地区医院和社区层面,分析了5岁以下不同疟疾表现儿童中恶性疟原虫msp-2基因的等位基因多态性。共有405名儿童(107例严重疟疾贫血病例、102例无严重贫血的严重疟疾病例和196例非严重疟疾病例)纳入研究。FC27在严重疟疾贫血儿童组中的频率为89.2%,在严重疟疾非贫血儿童病例和非严重疟疾病例中分别为89.7%和86.9%(P = 0.4)。3D7在严重疟疾非贫血儿童、严重疟疾贫血病例和非严重疟疾病例中的频率分别为72.5%、84.1%和77%(P = 0.7)。与非严重疟疾儿童相比,严重疟疾(有或无严重贫血)儿童中FC27基因型的复杂性显著更高(P << 0.001)。3D7基因型的复杂性未发现显著差异。