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首页> 外文期刊>Parasitology >The knockdown of each component of the cysteine proteinase-adhesin complex of Entamoeba histolytica (EhCPADH) affects the expression of the other complex element as well as the in vitro and in vivo virulence
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The knockdown of each component of the cysteine proteinase-adhesin complex of Entamoeba histolytica (EhCPADH) affects the expression of the other complex element as well as the in vitro and in vivo virulence

机译:Entamoeba histolytica(EhCPADH)的半胱氨酸蛋白酶-粘附素复合物的每个成分的敲低都会影响其他复合元件的表达以及体外和体内的毒力

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Entamoeba histolytica is the protozoan parasite causative of human amoebiasis, disease responsible for 40 000-100 000 deaths annually. The cysteine proteinase-adhesin complex of this parasite (EhCPADH) is a heterodimeric protein formed by a cysteine protease (EhCP112) and an adhesin (EhADH) that plays an important role in the cytopathic mechanism of this parasite. The coding genes for EhCP112 and EhADH are adjacent in the E. histolytica genome, suggesting that their expression may be co-regulated, but this hypothesis has not yet been confirmed. Here, we performed the knockdown of EhCP112 and EhADH using gene-specific short-hairpin RNAs (shRNA), and the effect of these knockdowns on the expression of both complex components as well as on the in vitro and in vivo virulence was analysed. Results showed that the knockdown of one of the EhCPADH components produced a simultaneous downregulation of the other protein. Accordingly, a concomitant reduction in the overall expression of the complex was observed. The downregulation of each component also produced a significant decrease in the in vitro and in vivo virulence of trophozoites. These results demonstrated that the expression of EhCP112 and EhADH is co-regulated and confirmed that the EhCPADH complex plays an important role in E. histolytica virulence.
机译:溶血性变形杆菌是引起人类阿米巴病的原生动物寄生虫,这种疾病每年导致4万至10万例死亡。该寄生虫的半胱氨酸蛋白酶-粘附素复合物(EhCPADH)是由半胱氨酸蛋白酶(EhCP112)和粘附素(EhADH)形成的异二聚体蛋白,在该寄生虫的细胞病变机理中起重要作用。 EhCP112和EhADH的编码基因在溶组织性大肠杆菌中是相邻的,这表明它们的表达可能受到共同调控,但是这一假设尚未得到证实。在这里,我们使用基因特异性短发夹RNA(shRNA)进行了EhCP112和EhADH的敲除,并分析了这些敲除对复杂成分表达以及体外和体内毒力的影响。结果显示,敲除一种EhCPADH成分会同时下调另一种蛋白质。因此,观察到复合物总表达的伴随减少。每种成分的下调也使滋养体的体外和体内毒力显着降低。这些结果表明,EhCP112和EhADH的表达是共同调节的,并证实EhCPADH复合物在溶血性大肠杆菌中具有重要作用。

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