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多房棘球绦虫成虫层状层相关蛋白的鉴定

Identification of a laminated layer-associated protein in Echinococcus multilocularis metacestodes.

作者信息

Ingold K, Gottstein B, Hemphill A

机构信息

Institute of Parasitology, University of Berne, Switzerland.

出版信息

Parasitology. 1998 Apr;116 ( Pt 4):363-72. doi: 10.1017/s0031182098002406.

Abstract

Echinococcus multilocularis is a cestode parasite that predominantly infects red and arctic foxes as definitive hosts. Ingestion of E. multilocularis eggs and subsequent post-oncospheral infection with the larval stage (metacestode) of the parasite results in alveolar echinococcosis (AE), a life-threatening hepatic disease concerning humans and other intermediate hosts such as small rodents. The primary fluid-filled vesicles of the asexually proliferating metacestode are comprised of an inner germinal layer, a syncytial tegument, and an outer, acellular, so-called laminated layer. This laminated layer may play an important role in protecting the developing E. multilocularis metacestode from host immune reactions, and laminated layer-associated components represent potential targets for intervention during the course of AE. We have used an in vitro cultivation technique for the long-term maintenance and proliferation of E. multilocularis metacestodes in order to generate premature (protoscolex-free) parasite vesicles. A polyclonal antiserum was raised against this host-free parasite tissue. Subsequent immunoblot analysis of parasite fractions obtained by Triton X-114 extraction lead to the identification of a 116 kDa protein (named EmP2) within the Triton-insoluble fraction. The characterization of EmP2 by SDS-PAGE, Western blotting, and by immunofluorescence revealed that EmP2 is a laminated layer-associated protein.

摘要

多房棘球绦虫是一种主要感染赤狐和北极狐作为终末宿主的绦虫寄生虫。摄入多房棘球绦虫虫卵以及随后被该寄生虫幼虫期(棘球蚴)的后尾蚴感染会导致泡型包虫病(AE),这是一种危及人类和其他中间宿主(如小型啮齿动物)生命的肝脏疾病。无性增殖的棘球蚴的主要充满液体的囊泡由内生发层、合胞体皮层和外层无细胞的所谓板层组成。该板层可能在保护发育中的多房棘球绦虫棘球蚴免受宿主免疫反应方面发挥重要作用,并且与板层相关的成分是AE病程中干预的潜在靶点。我们使用体外培养技术长期维持和增殖多房棘球绦虫棘球蚴,以产生未成熟(无原头节)的寄生虫囊泡。针对这种无宿主的寄生虫组织制备了多克隆抗血清。随后对通过Triton X - 114提取获得的寄生虫组分进行免疫印迹分析,在Triton不溶性组分中鉴定出一种116 kDa的蛋白质(命名为EmP2)。通过SDS - PAGE、蛋白质印迹和免疫荧光对EmP2进行表征,结果表明EmP2是一种与板层相关的蛋白质。

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