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多房棘球绦虫和细粒棘球绦虫全长抗原II/3的比较分析

Comparative analysis of full-length antigen II/3 from Echinococcus multilocularis and E. granulosus.

作者信息

Felleisen R, Gottstein B

机构信息

Institute of Parasitology, University of Berne, Switzerland.

出版信息

Parasitology. 1994 Aug;109 ( Pt 2):223-32. doi: 10.1017/s0031182000076344.

DOI:10.1017/s0031182000076344
PMID:7521956
Abstract

The recombinant Echinococcus multilocularis antigen II/3-10 is one of the most promising tools for immunodiagnosis of alveolar echinococcosis in human patients. Its nucleic acid sequence represents a part of the E. multilocularis gene encoding the metacestode antigen II/3, the former being basically present and expressed in both E. multilocularis and E. granulosus. Most (94%) patients with alveolar echinococcosis respond to infection with a marked anti-II/3-10 IgG synthesis; in contrast, most of the cystic echinococcosis patients do not, for some reason, recognize the recombinant antigen. We tackled this problem by generating cDNA derived from both E. granulosus and E. multilocularis full length II/3 genes, performed by reverse transcription and PCR amplification. Sequence analysis revealed a very high degree of conservation of the primary sequence of the antigen II/3 in both Echinococcus species. cDNA fragments were subcloned and expressed in E. coli as fusion proteins with Schistosoma japonicum glutathione S-transferase. Recombinant proteins were affinity purified and comparatively assessed by ELISA with respect to antibody-binding characteristics. Sera from patients suffering from cystic echinococcosis showed no significant differences in reactivity with the antigens derived from either E. multilocularis or E. granulosus. Therefore, parameters other than some minor differences in the primary sequence seem to be responsible for the lack of antigen II/3 recognition in cystic echinococcosis.

摘要

重组多房棘球绦虫抗原II/3 - 10是人类肺泡型棘球蚴病免疫诊断中最有前景的工具之一。其核酸序列代表多房棘球绦虫编码成虫蚴抗原II/3的基因的一部分,该基因基本同时存在于多房棘球绦虫和细粒棘球绦虫中并表达。大多数(94%)肺泡型棘球蚴病患者感染后会显著合成抗II/3 - 10 IgG;相比之下,大多数囊性棘球蚴病患者由于某种原因无法识别这种重组抗原。我们通过逆转录和PCR扩增,从细粒棘球绦虫和多房棘球绦虫的全长II/3基因中生成cDNA来解决这个问题。序列分析显示两种棘球绦虫物种中抗原II/3的一级序列具有高度保守性。将cDNA片段亚克隆并在大肠杆菌中表达为与日本血吸虫谷胱甘肽S - 转移酶的融合蛋白。对重组蛋白进行亲和纯化,并通过ELISA对其抗体结合特性进行比较评估。囊性棘球蚴病患者的血清与多房棘球绦虫或细粒棘球绦虫来源的抗原反应性无显著差异。因此,除了一级序列中的一些微小差异外,其他参数似乎是导致囊性棘球蚴病中缺乏对抗原II/3识别的原因。

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