Qari S H, Shi Y P, Goldman I F, Nahlen B L, Tibayrenc M, Lal A A
Division of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Mol Biochem Parasitol. 1998 May 1;92(2):241-52. doi: 10.1016/s0166-6851(98)00010-3.
The 19-kDa antigenic domain of Plasmodium falciparum merozoite surface protein (MSP)-1 is a potential malaria vaccine candidate. Based on the amino acid substitution, four known alleles, E-TSR (PNG-MAD20 type), E-KNG (Uganda-PA type), Q-KNG (Wellcome type), and Q-TSR (Indo type) of this domain have been identified. Using single or double crossover recombinational events, we predicted the existence of additional alleles of this antigen. The presence of the predicted alleles was determined in parasite isolates from western Kenya, by undertaking a cross-sectional and a longitudinal study. Of the ten predicted alleles, we have revealed the presence of three new alleles: E-KSG-L (Kenya-1 type); E-KSR-L (Kenya-2 type); and E-KNG-F (Kenya-3 type). The results of this study suggest that it may be possible to predict the complexity of the genetic makeup of natural parasite populations.
恶性疟原虫裂殖子表面蛋白(MSP)-1的19-kDa抗原结构域是一种潜在的疟疾疫苗候选物。基于氨基酸替换,已鉴定出该结构域的四个已知等位基因,即E-TSR(巴布亚新几内亚-MAD20型)、E-KNG(乌干达-PA型)、Q-KNG(威康型)和Q-TSR(印度型)。利用单交换或双交换重组事件,我们预测了该抗原其他等位基因的存在。通过进行横断面研究和纵向研究,在肯尼亚西部的寄生虫分离株中确定了预测等位基因的存在。在十个预测等位基因中,我们发现了三个新等位基因:E-KSG-L(肯尼亚-1型);E-KSR-L(肯尼亚-2型);以及E-KNG-F(肯尼亚-3型)。这项研究的结果表明,有可能预测天然寄生虫群体基因组成的复杂性。