Khan Shahid M, Waters Andrew P
Department of Parasitology, Centre of Infectious Disease, Leiden University Medical Centre, Albinusdreef 1, 2333 ZA Leiden, The Netherlands.
Trends Parasitol. 2004 Dec;20(12):575-80. doi: 10.1016/j.pt.2004.10.001.
The Molecular Approaches to Malaria 2004 meeting provided an opportunity to see the impressive progress in all research fields and in the four years since the previous Molecular Approaches to Malaria meeting, when much of the Plasmodium falciparum genome sequence was already available. Study of the part of the Plasmodium life cycle associated with transmission through the vector, which begins with the commitment of blood-stage forms to sexual development, has been especially fruitful. This success is a result of several reasons including: (i) the availability of the genome sequence; (ii) the availability of good animal models that allow parasite culture and facile in vivo studies of many of the life cycle stages involved in transmission; (iii) the availability of genetic manipulation technologies for the animal models of malaria, as well as P. falciparum; and (iv) the ability to study lethal gene knockouts at this stage of the life cycle.
2004年疟疾分子研究会议提供了一个契机,得以见证所有研究领域取得的令人瞩目的进展。自上一次疟疾分子研究会议以来的四年间,恶性疟原虫的大部分基因组序列已可获取。对疟原虫生命周期中与通过媒介传播相关部分的研究,即从血液阶段形式向有性发育的转变开始,成果尤为丰硕。这一成功得益于多种因素,包括:(i)基因组序列的可获取性;(ii)有良好的动物模型,可用于寄生虫培养以及对传播过程中涉及的许多生命周期阶段进行便捷的体内研究;(iii)具备针对疟疾动物模型以及恶性疟原虫的基因操作技术;(iv)能够在生命周期的这一阶段研究致死性基因敲除。