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首页> 外文期刊>Letters in Applied Microbiology >Reverse transcription loop-mediated isothermal amplification (RT-LAMP) combined with colorimetric gold nanoparticle (AuNP) probe assay for visual detection of Penaeus vannamei nodavirus (PvNV).
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Reverse transcription loop-mediated isothermal amplification (RT-LAMP) combined with colorimetric gold nanoparticle (AuNP) probe assay for visual detection of Penaeus vannamei nodavirus (PvNV).

机译:逆转录环介导的等温扩增(RT-LAMP)与比色金纳米颗粒(AuNP)探针检测相结合,用于视觉检测南美白对虾诺德病毒(PvNV)。

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摘要

Penaeus vannamei nodavirus (PvNV) is an emerging viral infection that has caused muscle necrosis or a white tail disease in cultivated whiteleg shrimp Penaeus (Litopenaeus) vannamei, leading to loss in the productions. Rapid detection of PvNV is essential for further control disease. A combination between reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay and colorimetric gold nanoparticle (AuNP) probe was developed for rapid, sensitive and inexpensive detection of PvNV in this study. RT-LAMP reaction successfully detected PvNV at 63 degrees C for 45 and 5 min for hybridization of LAMP amplified product, followed by salt-induced AuNP-labelled ssDNA probe aggregation to visual colour development. This method showed identical results to LAMP followed by gel electrophoresis and spectrophotometric detection, and it was 10 times sensitive more than conventional nested RT-PCR. The new method revealed negative results with other shrimp pathogens. This study provides the direct visualization of LAMP reaction by AuNP probe hybridization, that significantly reduces the time and cost required for the molecular diagnostic of infectious diseases and offers to use in aquaculture health management.Digital Object Identifier http://dx.doi.org/10.1111/lam.12065
机译:南美白对虾诺达病毒(PvNV)是一种新兴的病毒感染,已经在养殖的白腿虾南美白对虾(Litopenaeus)南美白对虾中引起肌肉坏死或白尾病,导致产量下降。快速检测PvNV对于进一步控制疾病至关重要。这项研究中逆转录环介导的等温扩增(RT-LAMP)测定法与比色金纳米粒子(AuNP)探针相结合,可用于快速,灵敏和廉价地检测PvNV。 RT-LAMP反应成功地在63摄氏度下检测到45分钟和5分钟的PvNV以进行LAMP扩增产物的杂交,然后用盐诱导的AuNP标记的ssDNA探针聚合形成可见色。该方法的结果与LAMP相同,随后进行凝胶电泳和分光光度法检测,其灵敏度是常规嵌套式RT-PCR的10倍以上。新方法对其他虾病原体显示阴性结果。这项研究提供了通过AuNP探针杂交对LAMP反应进行直接可视化的方法,从而显着减少了传染病分子诊断所需的时间和成本,并可以用于水产养殖健康管理中。 /10.1111/lam.12065

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