Bozdech Zbynek, Mok Sachel, Hu Guangan, Imwong Mallika, Jaidee Anchalee, Russell Bruce, Ginsburg Hagai, Nosten Francois, Day Nicholas P J, White Nicholas J, Carlton Jane M, Preiser Peter R
School of Biological Sciences, Nanyang Technological University, Singapore 637551.
Proc Natl Acad Sci U S A. 2008 Oct 21;105(42):16290-5. doi: 10.1073/pnas.0807404105. Epub 2008 Oct 13.
Plasmodium vivax causes over 100 million clinical infections each year. Primarily because of the lack of a suitable culture system, our understanding of the biology of this parasite lags significantly behind that of the more deadly species P. falciparum. Here, we present the complete transcriptional profile throughout the 48-h intraerythrocytic cycle of three distinct P. vivax isolates. This approach identifies strain specific patterns of expression for subsets of genes predicted to encode proteins associated with virulence and host pathogen interactions. Comparison to P. falciparum revealed significant differences in the expression of genes involved in crucial cellular functions that underpin the biological differences between the two parasite species. These data provide insights into the biology of P. vivax and constitute an important resource for the development of therapeutic approaches.
间日疟原虫每年导致超过1亿例临床感染。主要由于缺乏合适的培养系统,我们对这种寄生虫生物学的了解显著落后于更致命的恶性疟原虫。在此,我们展示了三种不同间日疟原虫分离株在48小时红细胞内周期中的完整转录谱。这种方法确定了预测编码与毒力和宿主病原体相互作用相关蛋白质的基因子集的菌株特异性表达模式。与恶性疟原虫的比较揭示了参与关键细胞功能的基因表达存在显著差异,这些功能支撑了两种寄生虫物种之间的生物学差异。这些数据为间日疟原虫的生物学提供了见解,并构成了开发治疗方法的重要资源。