Takala Shannon L, Smith David L, Thera Mahamadou A, Coulibaly Drissa, Doumbo Ogobara K, Plowe Christopher V
Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
Am J Trop Med Hyg. 2007 May;76(5):855-9.
Genetic diversity in malaria vaccine antigens may compromise malaria vaccine efficacy, so it is important to understand this diversity and the processes that generate it. By applying new high-throughput genotyping methods to a large sample of infections from Mali (N = 1369), seven new 19-kDa merozoite surface protein 1 (MSP-1(19)) haplotypes were identified. Herein we report the sequences of these new haplotypes and discuss their possible origins. Although they are present in < 1% of the samples examined, the existence of these rare haplotypes reveals a greater degree of diversity at this locus than previously reported and highlights the potential for Plasmodium to evolve under selective pressure from the immune system and from such interventions as vaccines and drugs.
疟疾疫苗抗原的遗传多样性可能会损害疟疾疫苗的效力,因此了解这种多样性及其产生过程非常重要。通过将新的高通量基因分型方法应用于来自马里的大量感染样本(N = 1369),鉴定出了七种新的19-kDa裂殖子表面蛋白1(MSP-1(19))单倍型。在此我们报告这些新单倍型的序列并讨论它们可能的起源。尽管它们在所检测的样本中占比不到1%,但这些罕见单倍型的存在揭示了该位点的多样性程度比之前报道的更高,并突出了疟原虫在免疫系统以及疫苗和药物等干预措施的选择压力下进化的潜力。