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首页> 外文期刊>International journal of infectious diseases : >Asparaginyl endopeptidase from the carcinogenic liver fluke, Opisthorchis viverrini, and its potential for serodiagnosis
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Asparaginyl endopeptidase from the carcinogenic liver fluke, Opisthorchis viverrini, and its potential for serodiagnosis

机译:致癌性肝吸虫Opisthorchis viverrini的天冬酰胺基内肽酶及其血清学诊断潜力

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Objectives To isolate and characterize an asparaginyl endopeptidase from the carcinogenic liver fluke, Opisthorchis viverrini, and evaluate its expression profile, biochemical activity, and potential as an immunodiagnostic antigen. ; Methods The full length mRNA encoding an asparaginyl endopeptidase (family C13), Ov-aep-1, was isolated by immunoscreening of a cDNA bacteriophage library of adult O. viverrini using sera from patients infected with O. viverrini. Investigation of Ov-aep-1 transcripts in developmental stages of the parasite, and phylogenetic analysis, immunohistochemical localization, and recombinant protein expression and enzymology were employed to characterize the Ov-AEP-1 protein. Immunoblotting was used to assess the potential of this enzyme for immunodiagnosis of human opisthorchiasis. ; Results Ov-AEP-1 is characteristic of the C13 cysteine protease family. Ov-aep-1 transcripts were detected in adult and juvenile worms, eggs, and metacercariae. Phylogenetic analysis indicated that Ov-AEP-1 is closely related to homologous proteins in other trematodes. Recombinant Ov-AEP-1 was expressed in bacteria in inclusion bodies and refolded to a soluble form. Excretory–secretory (ES) products derived from adult O. viverrini and refolded recombinant Ov-AEP-1 both displayed catalytic activity against the diagnostic tripeptide substrate, Ala–Ala–Asn-aminomethylcoumarin. Rabbit antiserum raised to recombinant Ov-AEP-1 identified the native AEP-1 protease in both somatic extract and ES products of adult worms. Anti-Ov-AEP-1 IgG immunolocalized the anatomical site of expression to the gut of the fluke, implying a physiological role in digestion of food or activation of other digestive enzymes. Recombinant Ov-AEP-1 was recognized by serum antibodies from patients with opisthorchiasis but not other helminth infections, with a sensitivity and specificity of 85% and 100%, respectively. The positive and negative predictive values are 100% and 67%, respectively. ; Conclusions The liver fluke, O. viverrini, has a gut-localized asparaginyl endopeptidase. Refolded recombinant Ov-AEP-1 is catalytically active and has potential for immunodiagnosis of human opisthorchiasis.
机译:目的从致癌性肝吸虫(Opisthorchis viverrini)中分离并鉴定天冬酰胺基内肽酶,并评估其表达谱,生化活性和作为免疫诊断抗原的潜力。 ;方法使用感染了维氏弧菌的患者血清,通过免疫筛选成人维氏弧菌的cDNA噬菌体文库,分离出编码天冬酰胺基内肽酶(家族C13)Ov-aep-1的全长mRNA。研究寄生虫发育阶段的Ov-aep-1转录本,并进行系统发育分析,免疫组织化学定位以及重组蛋白表达和酶学来表征Ov-AEP-1蛋白。免疫印迹用于评估该酶对人阿霉素的免疫诊断的潜力。 ;结果Ov-AEP-1是C13半胱氨酸蛋白酶家族的特征。在成虫和幼虫,卵和尾cer中检测到Ov-aep-1转录本。系统发育分析表明,Ov-AEP-1与其他吸虫中的同源蛋白密切相关。重组Ov-AEP-1在细菌的包涵体中表达,并重新折叠成可溶形式。源自成虫O. viverrini的排泄分泌(ES)产品和重新折叠的重组Ov-AEP-1均显示出对诊断性三肽底物Ala-Ala-Asn-氨基甲基香豆素的催化活性。产生抗重组Ov-AEP-1的兔抗血清可在成虫的体细胞提取物和ES产品中鉴定出天然AEP-1蛋白酶。抗Ov-AEP-1 IgG将表达的解剖部位免疫定位在吸虫的肠道中,这暗示着在消化食物或激活其他消化酶方面的生理作用。重组Ov-AEP-1被来自阿米巴气菌病患者而非其他蠕虫感染患者的血清抗体识别,敏感性和特异性分别为85%和100%。阳性和阴性预测值分别为100%和67%。 ;结论肝吸虫O. viverrini具有肠道定位的天冬酰胺基内肽酶。重新折叠的重组Ov-AEP-1具有催化活性,具有对人阿霉素的免疫诊断潜力。

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