Paul R E, Hackford I, Brockman A, Muller-Graf C, Price R, Luxemburger C, White N J, Nosten F, Day K P
The Wellcome Trust Centre for the Epidemiology of Infectious Disease, Department of Zoology, Oxford University, United Kingdom.
Am J Trop Med Hyg. 1998 Feb;58(2):195-203. doi: 10.4269/ajtmh.1998.58.195.
Genetic analysis of the number of Plasmodium falciparum genotypes per infected person in regions of holoendemic and hyperendemic malaria suggest that in areas of lower transmission intensity, significantly fewer parasite genotypes per infected person should be found. A predominance of single clone infections in the human population could generate the controversial clonal population structure proposed for P. falciparum by Tibayrenc and others. Characterization of P. falciparum from individuals on the Thai-Burmese border, an area of hypoendemic transmission, revealed a higher number of genotypes per infected person than that predicted. Possible reasons for this observation are discussed, with particular attention paid to human migration and multidrug resistance.
在疟疾高度流行和超高度流行地区,对每个受感染个体中恶性疟原虫基因型数量的遗传分析表明,在传播强度较低的地区,每个受感染个体中发现的寄生虫基因型数量应显著减少。人群中单一克隆感染占主导地位可能会产生蒂巴伦克等人提出的关于恶性疟原虫的有争议的克隆种群结构。对泰国-缅甸边境这一低流行传播地区个体的恶性疟原虫进行特征分析,发现每个受感染个体的基因型数量高于预期。本文讨论了这一观察结果的可能原因,特别关注了人类迁移和多药耐药性。