首页> 外文期刊>The American Journal of Tropical Medicine and Hygiene >Performance of a Sandwich Antigen-Detection ELISA for the Diagnosis of Porcine Taenia solium Cysticercosis
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Performance of a Sandwich Antigen-Detection ELISA for the Diagnosis of Porcine Taenia solium Cysticercosis

机译:三明治抗原检测ELISA用于诊断猪Taenia菌囊霉菌病的性能

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摘要

The pig is the natural intermediate host of Taenia solium, a parasite causing significant burden of disease in both humans and pigs. Porcine cysticercosis is traditionally detected via tongue palpation and slaughterhouse meat inspection, both with limited sensitivity. Serum antibody detection has a better performance; however, it does not discriminate past from present infection. Serum antigen detection can demonstrate viable infection and gives a good estimate of parasitic load. This study evaluated a sandwich antigen-detection ELISA using monoclonal antibodies (MoAbs) 158C11 and 60H8 for the diagnosis of viable cysticercosis in pigs. Serum samples were used from 35 naturally T. solium cysticerci-infected pigs, 31 cysticercosis-negative pigs, and 22 pigs with Taenia hydatigena infection (to assess cross-reactions). Positive cysticercosis samples were subcategorized at necropsy according to parasitic burden as mild (1-10 viable cysts, n = 10), moderate (11-100 cysts, n = 5), or severe infection (more than 100 cysts, n = 20). This Ag-ELISA showed a sensitivity of 82.9% and a specificity of 96.8% when not considering cross-reactions with T. hydatigena. Hundred percentage of severely infected, 80% of moderately infected, and 50% of mildly T. solium-infected pigs tested positive. Twenty of 22 pigs with only T. hydatigena infections were positive, with 13 reaching saturating levels in the ELISA. The Ag-ELISA revealed the presence of live cysts and is, thus, a fairly reliable test to monitor experimental infection, response to treatment, and follow-up in animal models of cysticercosis. It should, however, be carefully interpreted when used in regions where T. hydatigena is endemic in pigs.
机译:猪是Taenia Solium的天然中间宿主,寄生虫在人类和猪中导致疾病的严重负担。传统上通过舌触发和屠宰场肉类检查检测猪膀胱术病,既有限敏感。血清抗体检测具有更好的性能;然而,它不会区分过去存在的感染。血清抗原检测可以证明可行的感染并给予寄生载荷的良好估计。本研究评估了使用单克隆抗体(MoAb)158C11和60H8进行夹层抗原检测ELISA,用于诊断猪中可行囊霉病的诊断。血清样品从35种天然T.源性肌霉菌感染的猪,31个囊尾蚴病阴性猪和22只猪,与Taenia Hydatena感染(以评估交叉反应)。根据寄生负荷,如温和(1-10可行囊肿,N = 10),中等(11-100囊肿,N = 5),或严重感染(超过100囊肿,n = 20) 。当不考虑与T. hydaTigena的交叉反应时,该Ag-ELISA显示出82.9%的敏感性为82.9%,特异性为96.8%。一百个百分比严重感染,80%的中度感染,50%的温和地T.感染的猪测试阳性。 22只只有T. hydaTigena感染的猪阳性,13次达到ELISA的饱和水平。 Ag-ELISA揭示了活囊肿的存在,因此是一种相当可靠的测试,可监测实验性感染,对治疗的反应以及囊尾蚴病的动物模型中的随访。然而,当在猪属特有的地区使用时,应该被仔细解释。

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