首页> 外文期刊>Veterinary Parasitology >Fasciola hepatica: Specificity of a coproantigen ELISA test for diagnosis of fasciolosis in faecal samples from cattle and sheep concurrently infected with gastrointestinal nematodes, coccidians and/or rumen flukes (paramphistomes), under field conditions
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Fasciola hepatica: Specificity of a coproantigen ELISA test for diagnosis of fasciolosis in faecal samples from cattle and sheep concurrently infected with gastrointestinal nematodes, coccidians and/or rumen flukes (paramphistomes), under field conditions

机译:肝Fasciola肝炎:协原酶ELISA试验在野外条件下诊断牛和羊粪便样品中同时感染了胃肠道线虫,球虫和/或瘤胃吸虫(副鞭毛)的粪便中的fasololosis

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Chronic fasciolosis is often diagnosed by faecal egg counting (FEC), following concentration of the eggs in the sample by a zinc sulphate floatation method. However, concentration by a sedimentation technique gives improved sensitivity. Interpretation of FEC results for fasciolosis is complicated by factors such as the long pre-patent period and irregular egg shedding. Thus, FEC reduction tests (FECRT), when used alone, are not completely reliable for diagnosis of anthelmintic susceptibility or resistance in local fluke populations, especially when parasite burdens are small. A Fasciola hepatica coproantigen ELISA test has been introduced which more accurately reflects the presence of flukes in the host bile ducts in late prepatent infections, and absence of flukes following successful chemotherapeutic intervention. The aim of the present study was to elucidate the specificity of the F. hepatica coproantigen ELISA technique, particularly regarding potential cross-reactivity with rumen fluke (paramphistome), gastrointestinal nematode and coccidian infections. The method involved parallel testing of a large battery of faecal samples from field-infected cattle and sheep using floatation and sedimentation FECs and coproantigen analysis. No evidence was found for significant false positivity in the F. hepatica coproantigen ELISA due to paramphistome, coccidian and/or gastrointestinal nematode co-infections. With sedimentation FECs less than 10 F. hepatica eggs per gram (epg), the likelihood of a positive coproantigen result for the sample progressively decreased. Diagnosis of fasciolosis should be based on consideration of both FEC and coproantigen ELISA findings, to ensure optimum sensitivity for pre-patent and low-level infections. (C) 2015 Elsevier B.V. All rights reserved.
机译:在通过硫酸锌浮选法对样品中的鸡蛋进行浓缩之后,通常通过粪便鸡蛋计数(FEC)来诊断慢性筋膜炎。但是,通过沉淀技术进行浓缩可以提高灵敏度。早熟期长和不规则卵脱落等因素使对筋膜病的FEC结果的解释变得复杂。因此,单独使用FEC降低测试(FECRT)不能完全可靠地诊断当地吸虫人群的驱虫药敏感性或耐药性,尤其是在寄生虫负担较小的情况下。已经引入了Fasciola hepatica coproantigen ELISA试验,该试验可以更准确地反映晚期晚期感染中宿主胆管中是否存在吸虫,并且在成功进行化学干预后仍不存在吸虫。本研究的目的是阐明肝炎链球菌原抗原ELISA技术的特异性,特别是关于与瘤胃吸虫(旁吸虫),胃肠线虫和球虫感染的潜在交叉反应性。该方法涉及使用浮选和沉降FEC和辅原抗原分析对来自田间感染牛和羊的大量粪便样品进行并行测试。由于旁淋巴组,球虫和/或胃肠道线虫的共感染,未在肝F.原抗原ELISA中发现明显假阳性的证据。当沉降的FEC小于每克10个肝鸡蛋时,样品中正原抗原阳性的可能性逐渐降低。 fasioolosis的诊断应基于FEC和辅助抗原ELISA的发现,以确保对专利前和低水平感染的最佳敏感性。 (C)2015 Elsevier B.V.保留所有权利。

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