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Roles of the Amino Terminal Region and Repeat Region of the Plasmodium berghei Circumsporozoite Protein in Parasite Infectivity

机译:氨基末端区域和寄生虫的感染性伯氏疟原虫孢子蛋白的重复区域的角色

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摘要

The circumsporozoite protein (CSP) plays a key role in malaria sporozoite infection of both mosquito salivary glands and the vertebrate host. The conserved Regions I and II have been well studied but little is known about the immunogenic central repeat region and the N-terminal region of the protein. Rodent malaria Plasmodium berghei parasites, in which the endogenous CS gene has been replaced with the avian Plasmodium gallinaceum CS (PgCS) sequence, develop normally in the A. stephensi mosquito midgut but the sporozoites are not infectious. We therefore generated P. berghei transgenic parasites carrying the PgCS gene, in which the repeat region was replaced with the homologous region of P. berghei CS (PbCS). A further line, in which both the N-terminal region and repeat region were replaced with the homologous regions of PbCS, was also generated. Introduction of the PbCS repeat region alone, into the PgCS gene, did not rescue sporozoite species-specific infectivity. However, the introduction of both the PbCS repeat region and the N-terminal region into the PgCS gene completely rescued infectivity, in both the mosquito vector and the mammalian host. Immunofluorescence experiments and western blot analysis revealed correct localization and proteolytic processing of CSP in the chimeric parasites. The results demonstrate, in vivo, that the repeat region of P. berghei CSP, alone, is unable to mediate sporozoite infectivity in either the mosquito or the mammalian host, but suggest an important role for the N-terminal region in sporozoite host cell invasion.
机译:环孢子蛋白(CSP)在疟疾唾液腺和脊椎动物宿主的疟疾孢子菌感染中起着关键作用。保守的区域I和II已经很好地研究,但是关于蛋白质的免疫原性中央重复区域和N-末端区域几乎熟知。啮齿动物疟疾疟原虫Perghei寄生虫,其中内源性Cs基因已被禽疟原虫Cs(PGCs)序列所取代,通常在A. Stephensi蚊子中肠,但孢子不是传染性的。因此,我们生成携带PGCS基因的P. Berghei转基因寄生虫,其中重复区域被P. Berghei Cs(PBCS)的同源区替换。还产生了另外的线,其中N-末端区域和重复区域都被PBC的同源区域取代。仅将PBCS重复区域引入PGCS基因中,并未拯救孢子沸石物种特异性感染性。然而,将PBC重复区域和N末端区域引入PGCS基因中完全拯救的感染性,蚊子载体和哺乳动物宿主。免疫荧光实验和Western印迹分析显示了CSP在嵌合寄生虫中的正确定位和蛋白水解加工。结果在体内表明,单独的P. Berghei CSP的重复区域不能在蚊子或哺乳动物宿主中介导孢子沸石感染性,但表明在孢子宿主体侵袭中对N-末端区域的重要作用。

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