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Identification of Tissue Cyst Wall Components by Transcriptome Analysis of In Vivo and In Vitro Toxoplasma gondii Bradyzoites

机译:体内和体外弓形虫慢摇子的转录组分析鉴定组织囊肿壁成分

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The Toxoplasma gondii bradyzoite is essential to establish persistent infection, yet little is known about what factors this developmental form secretes to establish the cyst or interact with its host cell. To identify candidate bradyzoite-secreted effectors, the transcriptomes of in vitro tachyzoites 2 days postinfection, in vitro bradyzoites 4 days postinfection, and in vivo bradyzoites 21 days postinfection were interrogated by microarray, and the program SignalP was used to identify signal peptides indicating secretion. One hundred two putative bradyzoite-secreted effectors were identified by this approach. Two candidates, bradyzoite pseudokinase 1 and microneme adhesive repeat domain-containing protein 4, were chosen for further investigation and confirmed to be induced and secreted by bradyzoites in vitro and in vivo. Thus, we report the first analysis of the transcriptomes of in vitro and in vivo bradyzoites and identify two new protein components of the Toxoplasma tissue cyst wall.
机译:刚地弓形虫缓殖子对于建立持续感染至关重要,但对于这种发育形式分泌形成囊肿或与其宿主细胞相互作用的因素知之甚少。为了鉴定候选的缓殖子分泌的效应子,通过微阵列询问感染后2天的体外速殖子,感染后4天的体外缓殖子和感染后21天的体内慢速子的转录组,并使用SignalP程序识别指示分泌的信号肽。通过这种方法鉴定了一百二十个假定的缓殖子分泌的效应子。选择了两种候选物,即缓殖子假激酶1和含有微neme重复序列的重复域蛋白4,以进行进一步研究,并确认它们是由缓殖子在体外和体内诱导和分泌的。因此,我们报告了体外和体内缓殖子的转录组的首次分析,并鉴定了弓形体组织囊肿壁的两个新的蛋白质成分。

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