Kappe S H, Gardner M J, Brown S M, Ross J, Matuschewski K, Ribeiro J M, Adams J H, Quackenbush J, Cho J, Carucci D J, Hoffman S L, Nussenzweig V
Michael Heidelberger Division, Department of Pathology, Kaplan Cancer Center, New York University School of Medicine, New York, NY 10016, USA.
Proc Natl Acad Sci U S A. 2001 Aug 14;98(17):9895-900. doi: 10.1073/pnas.171185198. Epub 2001 Aug 7.
Most studies of gene expression in Plasmodium have been concerned with asexual and/or sexual erythrocytic stages. Identification and cloning of genes expressed in the preerythrocytic stages lag far behind. We have constructed a high quality cDNA library of the Plasmodium sporozoite stage by using the rodent malaria parasite P. yoelii, an important model for malaria vaccine development. The technical obstacles associated with limited amounts of RNA material were overcome by PCR-amplifying the transcriptome before cloning. Contamination with mosquito RNA was negligible. Generation of 1,972 expressed sequence tags (EST) resulted in a total of 1,547 unique sequences, allowing insight into sporozoite gene expression. The circumsporozoite protein (CS) and the sporozoite surface protein 2 (SSP2) are well represented in the data set. A BLASTX search with all tags of the nonredundant protein database gave only 161 unique significant matches (P(N) < or = 10(-4)), whereas 1,386 of the unique sequences represented novel sporozoite-expressed genes. We identified ESTs for three proteins that may be involved in host cell invasion and documented their expression in sporozoites. These data should facilitate our understanding of the preerythrocytic Plasmodium life cycle stages and the development of preerythrocytic vaccines.
大多数关于疟原虫基因表达的研究都集中在无性和/或有性红细胞阶段。对疟原虫前期阶段表达的基因进行鉴定和克隆则远远滞后。我们利用啮齿动物疟原虫约氏疟原虫构建了高质量的疟原虫子孢子阶段的cDNA文库,约氏疟原虫是疟疾疫苗研发的重要模型。在克隆之前,通过对转录组进行PCR扩增克服了与RNA材料量有限相关的技术障碍。蚊子RNA的污染可以忽略不计。生成1972个表达序列标签(EST),共得到1547个独特序列,从而深入了解子孢子基因表达。环子孢子蛋白(CS)和子孢子表面蛋白2(SSP2)在数据集中有很好的体现。用非冗余蛋白质数据库的所有标签进行BLASTX搜索,仅得到161个独特的显著匹配项(P(N)≤10(-4)),而1386个独特序列代表了新的子孢子表达基因。我们鉴定了三种可能参与宿主细胞入侵的蛋白质的EST,并记录了它们在子孢子中的表达。这些数据应有助于我们了解疟原虫前期生命周期阶段以及前期疫苗的研发。