首页> 外文期刊>Biologicals: Journal of the International Association of Biological Standardization >Probe-free and sensitive detection of diarrhea-causing pathogens using RT-PCR combined high resolution melting analysis
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Probe-free and sensitive detection of diarrhea-causing pathogens using RT-PCR combined high resolution melting analysis

机译:使用RT-PCR和高分辨率熔解分析技术无需探针即可灵敏地检测引起腹泻的病原体

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摘要

Rapid and sensitive diagnostic methods are needed to help physicians make faster and better treatment decision for patients suffered from diarrhea. In the present study, a probe-free and sensitive RT-PCR combined high resolution melting analysis (HRMA) assay was established successfully for the detection of four major diarrhea-causing pathogens. The lower limit of detection of the assay were 10,102,10 and 10(3) copies/reaction for rotaviruses group A, astroviruses serotype 1, noroviruses genogroup II, and sapoviruses genegroup I, respectively, which were 1000-fold, 10-fold, 1000-fold and 10-fold more sensitive than conventional RT-PCR assay developed in parallel and comparable to or higher than commercially available real-time RT-PCR assay. Blinded sample evaluation showed that the assay was 100% concordant to both conventional RT-PCR and commercial real-time RT-PCR, indicating high reliability of the new assay. Therefore, the assay could provide a valuable platform for the probe-free and sensitive diagnosis of these pathogens. (C) 2016 International Alliance for Biological Standardization. Published by Elsevier Ltd. All rights reserved.
机译:需要快速而灵敏的诊断方法来帮助医生更快,更好地确定腹泻患者的治疗决策。在本研究中,成功​​建立了无探针和灵敏的RT-PCR结合高分辨率熔解分析(HRMA)分析法,用于检测四种引起腹泻的主要病原体。轮状病毒A组,星状病毒血清型1,诺如病毒基因组II和Sapoviruses基因组I的检测下限分别为10、102、10和10(3)个拷贝/反应,分别是1000倍,10倍,与并行开发的常规RT-PCR分析相比,其灵敏度高出1000倍和10倍,与市售实时RT-PCR分析相当或更高。盲法样品评估表明该测定与常规RT-PCR和商业实时RT-PCR均100%一致,表明该新测定具有很高的可靠性。因此,该测定法可以为这些病原体的无探针和敏感诊断提供有价值的平台。 (C)2016国际生物标准化联盟。由Elsevier Ltd.出版。保留所有权利。

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