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华支睾吸虫一个编码体表蛋白的新基因的分子克隆与鉴定

Molecular cloning and identification of a novel Clonorchis sinensis gene encoding a tegumental protein.

作者信息

Zhou Zhenwen, Hu Xuchu, Huang Yan, Hu Huixia, Ma Changling, Chen Xiaoxiang, Hu Fengyu, Xu Jin, Lu Fangli, Wu Zhongdao, Yu Xinbing

机构信息

Department of Parasitology, Medicine School of Sun Yat-Sen University, 74 Zhongshan 2nd road, Guangzhou 510089, People's Republic of China.

出版信息

Parasitol Res. 2007 Aug;101(3):737-42. doi: 10.1007/s00436-007-0541-8. Epub 2007 May 3.

DOI:10.1007/s00436-007-0541-8
PMID:17476530
Abstract

The tegumental membrane of platyhelminth parasites is of crucial importance for modulation of the host response and parasite survival. A cDNA encoding a novel tegumental protein 20.8 kDa (TP20.8) was found by large-scale sequencing of a Clonorchis sinensis cDNA library. This new cDNA was 755 bp long containing an open reading frame of 555 bp, which encoded a 20.8-kDa protein with an isoelectric point of 4.33. The deduced amino acid sequence exhibits 40 and 37% identity to Schistosoma japonicum sj20.8 and Schistosoma mansoni Sm 20.8, respectively. TP20.8 transcripts were detected in the adult worm and metacercariae cDNA libraries of C. sinensis but not in the egg. Recombinant C. sinensis TP20.8 protein was produced and purified from Escherichia coli BL21. Using specific anti-recombinant TP20.8 protein sera, the TP20.8 protein was immunohistochemically localized to the outer-surface membrane of C. sinensis. The specificity and sensitivity of the recombinant antigen for serologic diagnosis was assessed by enzyme-linked immunosorbent assay using serum from 100 patients with clonorchiasis, 20 patients with schistosomiasis, and 30 negative controls. The sensitivity was 68%, and the specificity was 84%. The antigen was less useful for the serodiagnosis of clonorchiasis with IgG.

摘要

扁形虫寄生虫的皮层膜对于调节宿主反应和寄生虫存活至关重要。通过对华支睾吸虫cDNA文库进行大规模测序,发现了一个编码新型皮层蛋白20.8 kDa(TP20.8)的cDNA。这个新的cDNA长755 bp,包含一个555 bp的开放阅读框,编码一个等电点为4.33的20.8 kDa蛋白。推导的氨基酸序列与日本血吸虫sj20.8和曼氏血吸虫Sm 20.8分别具有40%和37%的同一性。在华支睾吸虫的成虫和后尾蚴cDNA文库中检测到了TP20.8转录本,但在虫卵中未检测到。从大肠杆菌BL21中产生并纯化了重组华支睾吸虫TP20.8蛋白。使用特异性抗重组TP20.8蛋白血清,通过免疫组织化学将TP20.8蛋白定位到华支睾吸虫的外表面膜。使用100例华支睾吸虫病患者、20例血吸虫病患者和30例阴性对照的血清,通过酶联免疫吸附试验评估重组抗原用于血清学诊断的特异性和敏感性。敏感性为68%,特异性为84%。该抗原对IgG检测华支睾吸虫病的血清诊断价值较小。

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