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使用细粒棘球绦虫原头节和六钩蚴抗原评估用于诊断犬自然感染细粒棘球绦虫的血清学检测系统。

Evaluation of a serological test system for the diagnosis of natural Echinococcus granulosus infection in dogs using E. granulosus protoscolex and oncosphere antigens.

作者信息

Gasser R B, Lightowlers M W, Obendorf D L, Jenkins D J, Rickard M D

机构信息

University of Melbourne, Veterinary Clinical Centre, Werribee, Victoria.

出版信息

Aust Vet J. 1988 Dec;65(12):369-73. doi: 10.1111/j.1751-0813.1988.tb14274.x.

DOI:10.1111/j.1751-0813.1988.tb14274.x
PMID:3223848
Abstract

Serum antibody responses in feral or domesticated dogs naturally infected with Echinococcus granulosus or/and other common helminths were examined in an enzyme-linked immunosorbent assay (ELISA) using antigens prepared from E. granulosus protoscoleces or oncospheres. The ELISA using the protoscolex antigen was optimised with serums from experimental dogs monospecifically infected with E. granulosus or other helminth parasites, and helminth-free dogs. Anti-protoscolex antibody was detected in 16 of 22 (72.7%) serums from feral dogs with E. granulosus burdens ranging from 300 to 302,600 worms per dog. Seven serums from feral dogs which did not harbour E. granulosus at autopsy but which originated from an endemic hydatid region were tested using protoscolex antigen, and 1 serum gave a positive reaction. One hundred and two serums from dogs known never to have been infected with E. granulosus all gave negative reactions to protoscolex antigen. The sensitivity of the ELISA test proved to be superior to that which has been achieved by arecoline purging as a method of diagnosis for E. granulosus infection in dogs. For use of the assay in hydatid control or eradication campaigns, its sensitivity can be increased by choosing a lower absorbance discrimination value above which serums are regarded as having positive reactions. However, this does introduce positive reactions of some serums from dogs infected with helminths other than E. granulosus. In further development of the assay, use of defined recombinant antigens may improve both sensitivity and specificity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用由细粒棘球绦虫原头节或六钩蚴制备的抗原,通过酶联免疫吸附测定(ELISA)检测自然感染细粒棘球绦虫或/和其他常见蠕虫的野生或家养犬的血清抗体反应。使用原头节抗原的ELISA用实验性单特异性感染细粒棘球绦虫或其他蠕虫寄生虫的犬以及无蠕虫犬的血清进行了优化。在每只犬携带300至302,600条细粒棘球绦虫的22只野生犬的血清中,有16只(72.7%)检测到抗原头节抗体。对7份来自尸检时未发现细粒棘球绦虫但来自地方性包虫病流行区的野生犬血清,使用原头节抗原进行检测,其中1份血清呈阳性反应。已知从未感染过细粒棘球绦虫的102只犬的血清对原头节抗原均呈阴性反应。ELISA检测的敏感性被证明优于槟榔碱驱虫法,槟榔碱驱虫法是犬细粒棘球绦虫感染的一种诊断方法。为了在包虫病控制或根除运动中使用该检测方法,可以通过选择较低的吸光度判别值来提高其敏感性,高于该值的血清被视为呈阳性反应。然而,这确实会导致一些感染非细粒棘球绦虫的犬血清出现阳性反应。在该检测方法的进一步开发中,使用确定的重组抗原可能会提高敏感性和特异性。(摘要截断于250字)

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