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首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Multiplex PCR for the detection and quantification of zoonotic taxa of Giardia, Cryptosporidium and Toxoplasma in wastewater and mussels
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Multiplex PCR for the detection and quantification of zoonotic taxa of Giardia, Cryptosporidium and Toxoplasma in wastewater and mussels

机译:多重PCR用于废水和贻贝中贾第虫,隐孢子虫和弓形虫的人畜共患生物分类的检测和定量

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摘要

Giardia duodenalis, Cryptosporidium parvum and Toxoplasma gondii are important parasitic protists linked to water- and food-borne diseases. The accurate detection of these pathogens is central to the diagnosis, tracking, monitoring and surveillance of these protists in humans, animals and the environment. In this study, we established a multiplex real-time PCR (qPCR), coupled to high resolution melting (HRM) analysis, for the specific detection and quantification of each G. duodenalis (assemblage A), C parvum and T. gondii (Type I). Once optimised, this assay was applied to the testing of samples (n = 232) of treated wastewater and mussels (Mytilus galloprovincialis). Of 119 water samples, 28.6% were test-positive for G. duodenalis, C parvum and/or both pathogens; of 113 mussel samples, 66.6% were test-positive for G. duodenalis, C parvum and/or both pathogens, and 13.2% were test-positive for only T gondii. The specificity of all amplicons produced was verified by direct sequencing. The oo/cysts numbers (per 5 mu l of DNA sample) ranged from 10 to 64. The present multiplex assay achieved an efficiency of 100% and a R-2 value of >0.99. Current evidence indicates that this assay provides a promising tool for the simultaneous detection and quantitation of three key protist taxa. (C) 2015 Elsevier Ltd. All rights reserved.
机译:贾第鞭毛虫,小隐孢子虫和弓形虫是与水和食源性疾病相关的重要寄生生物。这些病原体的准确检测对于在人类,动物和环境中诊断,跟踪,监视和监视这些原生生物至关重要。在这项研究中,我们建立了多重实时PCR(qPCR),并与高分辨率熔解(HRM)分析相结合,用于特定的检测和定量十二指肠G. duodenalis(组合A),细小C. parvum和T. gondii(类型一世)。优化后,该测定法将用于测试处理过的废水和贻贝(Mytilus galloprovincialis)的样品(n = 232)。在119个水样中,有28.6%的十二指肠球菌,小球藻和/或两种病原体呈阳性。在113个贻贝样品中,66.6%的十二指肠球菌,小球藻和/或两种病原体呈阳性,而13.2%的氏菌T刚体呈阳性。通过直接测序验证了所产生的所有扩增子的特异性。 oo /囊肿数(每5微升DNA样品)在10到64之间。本发明的多重检测效率为100%,R-2值> 0.99。当前证据表明,该测定法为同时检测和定量三个主要原生生物分类群提供了有前途的工具。 (C)2015 Elsevier Ltd.保留所有权利。

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