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首页> 外文期刊>International Journal for Parasitology >A novel monoclonal antibody-based immunoenzymatic assay for epidemiological surveillance of the vector snails of Fasciola hepatica (Trematoda: Digenea)
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A novel monoclonal antibody-based immunoenzymatic assay for epidemiological surveillance of the vector snails of Fasciola hepatica (Trematoda: Digenea)

机译:一种新颖的基于单克隆抗体的免疫酶检测方法,用于流行性肝片吸虫(Fasciola hepatica)(Trematoda:Digenea)的蜗牛的流行病学监测

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摘要

Fasciolosis is a globally distributed snail-borne disease which requires economic consideration due to its enormous impact on veterinary medicine. During recent decades, this parasitosis has also shown increasing prevalence in human populations worldwide. The dissemination and successful transmission of fasciolosis ultimately depends on the existence of susceptible snails that act as intermediate hosts. Therefore, to accomplish effective control of this disease, surveillance and detection of the infected intermediate host would be essential. The screening of trematodes within snails using classical parasitological examination of the larvae can be unreliable (sensitivity and specificity vary depending on the time of infection and the experience of the observer) and relatively costly when using molecular biological methods during large-scale monitoring. Here we propose a novel monoclonal antibody-based immunoenzymatic assay to detect ongoing Fasciola hepatica infection in lymnaeid snails. Anti-F. hepatica rediae mouse monoclonal antibodies were generated and used to develop a double monoclonal antibody-based ELISA for parasite detection. Fasciola hepatica-infected and uninfected laboratory-reared Galba cubensis and Pseudosuccinea columella were used for assessment of the developed ELISA. Experimentally infected snails were dissected and examined for parasite larvae as the "gold standard" method. Sensitivity results were 100% for both snail species, while specificity was 98% for G. cubensis and 100% for P. columella. No cross-reactivity was detected in lymnaeids infected with Trichobilharzia sp. or Cotylophoron sp. The ELISA enabled detection of the infection from day 8 p.i. in G. cubensis while in P. columella it was noted as early as day 4. To our knowledge no previous immunoassays have been reported to detect helminth-infected snails and the developed sandwich ELISA method is therefore suggested for infection status validation in natural populations of lymnaeid snails. (C) 2014 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.
机译:fasciolosis是一种由蜗牛传播的全球性疾病,由于其对兽药的巨大影响,因此需要进行经济考虑。在最近的几十年中,这种寄生虫病也显示出全世界人口的患病率正在上升。锦囊虫病的传播和成功传播最终取决于充当中间宿主的易感蜗牛的存在。因此,为了实现对该疾病的有效控制,对感染的中间宿主进行监测和检测将至关重要。使用经典的寄生虫寄生虫检查对蜗牛内的吸虫进行筛查可能是不可靠的(敏感性和特异性取决于感染时间和观察者的经验而异),并且在大规模监测中使用分子生物学方法时相对昂贵。在这里,我们提出了一种新型的基于单克隆抗体的免疫酶检测方法,以检测正在进行的Fasciola肝炎的蜗牛中的肝炎感染。反F。生成了肝重病小鼠单克隆抗体,并将其用于开发基于双单克隆抗体的ELISA用于寄生虫检测。用Fasciola肝感染的和未感染的实验室饲养的Galba立方霉菌和假单胞菌进行了评估。解剖实验感染的蜗牛,并检查寄生虫幼虫作为“金标准”方法。两种蜗牛的敏感性结果均为100%,而立方体革兰氏菌和小白僵菌的特异性结果均为98%。在感染了Trichobilharzia sp。的lymnaeids中未检测到交叉反应。或Cotylophoron sp。 ELISA可以从p.i第8天起检测感染。最早在第4天就发现了立方霉菌的存在。而据我们所知,以前没有进行免疫测定的方法可检测到蠕虫感染的蜗牛,因此建议使用已开发的三明治ELISA方法验证自然种群中的感染状况。 lymnaeid蜗牛。 (C)2014年澳大利亚寄生虫学协会。由Elsevier Ltd.出版。保留所有权利。

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