Mercereau-Puijalon Odile
Unité d'Immunologie Moléculaire des Parasites, CNRS URA 2581, Institut Pasteur, 25, rue du Docteur Roux, 75015 Paris, France.
J Soc Biol. 2004;198(3):193-7.
Genomic sequence determination of Plasmodium falciparum and other species of the genus, as well as that of Anopheles gambiae, and human, rat and mouse genome sequencing have completely changed the landscape of fundamental research about malaria. These data should urgently be exploited, in order to develop new tools to combat the disease: new drugs, fine dissection of the cascade of events following infection of the various vector species and vertebrate host, analysis of the complex interaction leading to the pathology or, inversely, contributing to sustained protection. Powerful population biology tools are now available, allowing to investigate genetic exchanges within natural population and to identify factors structuring parasitic and vector populations. Nevertheless, important impediments persist, including the complexity of experimental systems and the unclear relevance of animals models. Numerous challenges are to be faced; they call upon a more efficient organisation of research efforts in the systematic explorations using the powerful novel post-genomic technologies, as well as the development of new tools and experimental models required by functional genomics and integrative biology.
恶性疟原虫及该属其他物种的基因组序列测定,以及冈比亚按蚊、人类、大鼠和小鼠的基因组测序,彻底改变了疟疾基础研究的格局。这些数据应尽快加以利用,以开发抗击该疾病的新工具:新药物、详细剖析各种媒介物种和脊椎动物宿主感染后一系列事件、分析导致病理变化或相反有助于持续保护的复杂相互作用。现在已有强大的群体生物学工具,可用于研究自然种群内的基因交换,并识别构成寄生虫和媒介种群的因素。然而,重要障碍依然存在,包括实验系统的复杂性以及动物模型相关性不明确。仍有许多挑战需要面对;这些挑战要求在利用强大的新型后基因组技术进行系统探索时,更有效地组织研究工作,以及开发功能基因组学和整合生物学所需的新工具和实验模型。