基于单克隆抗体的荧光法检测猴免疫缺陷病毒感染猕猴粪便中双胞虫孢子的敏感性和特异性

Inderpal Singh, Abhineet S Sheoran, Quanshun Zhang, Angela Carville, Saul Tzipori
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引用次数: 21

摘要

在引起人类免疫缺陷病毒/艾滋病患者慢性腹泻、消瘦和胆管炎的微孢子虫中,bieneusenterocytozoon是临床上最重要的。用荧光或改性三色染色镜检是微孢子虫病的标准诊断试验,但不允许进行物种鉴定。基于PCR的比氏伊氏杆菌感染检测仅限于少数参考实验室,因此它不是标准的诊断方法。我们最近报道了一组抗布氏绦虫单克隆抗体的开发和鉴定,并在该出版物中评估了免疫荧光法(IFA)的特异性和敏感性,与PCR相比,在猴免疫缺陷病毒感染的猕猴中。与初级PCR方法相关的IFA检测限为每克粪便1.5 x 10(5)个孢子,将大大简化临床和环境标本以及实验室和流行病学调查中双胞杆菌孢子的检测。
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Sensitivity and specificity of a monoclonal antibody-based fluorescence assay for detecting Enterocytozoon bieneusi spores in feces of simian immunodeficiency virus-infected macaques.

Enterocytozoon bieneusi is clinically the most significant among the microsporidia causing chronic diarrhea, wasting, and cholangitis in individuals with human immunodeficiency virus/AIDS. Microscopy with either calcofluor or modified trichrome stains is the standard diagnostic test for microsporidiosis and does not allow species identification. Detection of E. bieneusi infection based on PCR is limited to a few reference laboratories, and thus it is not the standard diagnostic assay. We have recently reported the development and characterization of a panel of monoclonal antibodies against E. bieneusi, and in this publication we evaluated the specificity and sensitivity of an immunofluorescence assay (IFA), compared with PCR, in simian immunodeficiency virus-infected macaques. The IFA, which correlated with the primary PCR method, with a detection limit of 1.5 x 10(5) spores per gram of feces, will simplify considerably the detection of E. bieneusi spores in clinical and environmental specimens and in laboratory and epidemiological investigations.

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