Ocádiz-Ruiz Ramón, Fonseca Wendy, Linford Alicia S, Yoshino Timothy P, Orozco Esther, Rodríguez Mario A
Departamento de Infectómica y Patogénesis Molecular,CINVESTAV-IPN,México,D.F. México.
Department of Biochemistry and Molecular Genetics,University of Virginia Health System,Charlottesville,Virginia 22908,USA.
Parasitology. 2016 Jan;143(1):50-9. doi: 10.1017/S003118201500147X. Epub 2015 Nov 2.
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.
溶组织内阿米巴是引起人类阿米巴病的原生动物寄生虫,该疾病每年导致4万至10万人死亡。这种寄生虫的半胱氨酸蛋白酶 - 粘附素复合物(EhCPADH)是一种异源二聚体蛋白,由半胱氨酸蛋白酶(EhCP112)和一种粘附素(EhADH)组成,在该寄生虫的细胞病变机制中起重要作用。EhCP112和EhADH的编码基因在溶组织内阿米巴基因组中相邻,这表明它们的表达可能受到共同调控,但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)对EhCP112和EhADH进行了敲低,并分析了这些敲低对复合物两个组分的表达以及对体外和体内毒力的影响。结果表明,EhCPADH组分之一的敲低会导致另一种蛋白质同时下调。因此,观察到复合物的整体表达同时降低。每个组分的下调也导致滋养体在体外和体内的毒力显著降低。这些结果表明,EhCP112和EhADH的表达受到共同调控,并证实EhCPADH复合物在溶组织内阿米巴的毒力中起重要作用。