Chen Q, Fernandez V, Sundström A, Schlichtherle M, Datta S, Hagblom P, Wahlgren M
Microbiology and Tumor Biology Center, Karolinska Institutet, Stockholm, Sweden.
Nature. 1998 Jul 23;394(6691):392-5. doi: 10.1038/28660.
The protozoan Plasmodium falciparum causes lethal malaria. Adhesion of erythrocytes infected with P. falciparum to vascular endothelium and to uninfected red blood cells (rosetting) may be involved in the pathogenesis of severe malaria. The binding is mediated by the antigenically variant erythrocyte-membrane-protein-1 (PfEMP-1), which is encoded by members of the P. falciparum var gene family. The control of expression and switching of var genes seems to lack resemblance to mechanisms operating in variant gene families of other microbial pathogens. Here we show that multiple, distinct var gene transcripts (about 24 or more) can be detected by reverse transcription and polymerase chain reaction in bulk cultures of the rosetting parasite FCR3S1.2, despite the adhesive homogeneity of the cultures. We also detected several var transcripts in single erythrocytes infected with a ring-stage parasite of FCR3S1.2, and found that different var genes are transcribed simultaneously from several chromosomes in the same cell. In contrast, we detected only one var transcript, FCR3S1.2 var-1, which encodes the rosetting PfEMP-1 protein, in individual rosette-adhesive trophozoite-infected cells, and we found only one PfEMP-1 type at the erythrocyte surface by labelling with 125iodine and immunoprecipitation. We conclude that a single P. falciparum parasite simultaneously transcribes multiple var genes but, through a developmentally regulated process, selects only one PfEMP-1 to reach the surface of the host cell.
恶性疟原虫这种原生动物会引发致命的疟疾。感染恶性疟原虫的红细胞与血管内皮细胞以及未感染的红细胞(形成玫瑰花结)的黏附可能参与了重症疟疾的发病机制。这种结合是由抗原变异的红细胞膜蛋白1(PfEMP-1)介导的,PfEMP-1由恶性疟原虫var基因家族的成员编码。var基因表达和转换的调控机制似乎与其他微生物病原体变异基因家族的运作机制不同。在此我们表明,尽管玫瑰花结寄生虫FCR3S1.2的批量培养物具有黏附同质性,但通过逆转录和聚合酶链反应仍可检测到多个不同的var基因转录本(约24个或更多)。我们还在感染FCR3S1.2环状期寄生虫的单个红细胞中检测到了多个var转录本,并发现同一细胞中几个染色体上的不同var基因同时转录。相比之下,在单个感染玫瑰花结黏附滋养体的细胞中,我们仅检测到一个var转录本FCR3S1.2 var-1,它编码形成玫瑰花结的PfEMP-1蛋白,并且通过用125碘标记和免疫沉淀法,我们在红细胞表面仅发现了一种PfEMP-1类型。我们得出结论,单个恶性疟原虫寄生虫同时转录多个var基因,但通过一个发育调控过程,仅选择一种PfEMP-1到达宿主细胞表面。