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本文引用的文献

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A multiplex real-time PCR assay for rapid detection and differentiation of 25 bacterial and fungal pathogens from whole blood samples.一种用于从全血样本中快速检测和区分25种细菌和真菌病原体的多重实时PCR检测方法。
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Real-time RT-PCR assay for rapid and specific detection of classical swine fever virus: comparison of SYBR Green and TaqMan MGB detection methods using novel MGB probes.用于快速特异性检测猪瘟病毒的实时逆转录聚合酶链反应分析:使用新型MGB探针比较SYBR Green和TaqMan MGB检测方法
J Virol Methods. 2008 Feb;147(2):257-64. doi: 10.1016/j.jviromet.2007.09.017. Epub 2007 Nov 14.
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A TaqMan-based real-time PCR assay for the specific detection and quantification of Leuconostoc mesenteroides in meat products.一种基于TaqMan的实时PCR检测方法,用于肉类产品中嗜渗明串珠菌的特异性检测和定量分析。
FEMS Microbiol Lett. 2008 Jan;278(1):62-71. doi: 10.1111/j.1574-6968.2007.00974.x. Epub 2007 Nov 12.
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Comparison between quantitative nucleic acid sequence-based amplification, real-time reverse transcriptase PCR, and real-time PCR for quantification of Leishmania parasites.基于核酸序列的定量扩增、实时逆转录聚合酶链反应和实时聚合酶链反应在利什曼原虫定量检测中的比较。
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Quantitative study of persistence of human norovirus genome in water using TaqMan real-time RT-PCR.运用TaqMan实时逆转录聚合酶链反应对人诺如病毒基因组在水中的持久性进行定量研究。
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Applications of nanobiotechnology in clinical diagnostics.纳米生物技术在临床诊断中的应用。
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Detection and semi-quantification of Strongylus vulgaris DNA in equine faeces by real-time quantitative PCR.通过实时定量PCR检测和半定量马粪便中普通圆线虫DNA
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Identification of human pathogens isolated from blood using microarray hybridisation and signal pattern recognition.使用微阵列杂交和信号模式识别技术从血液中分离出人类病原体的鉴定。
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分子诊断方法在食品安全中的潜力和局限性。

Potentials and limitations of molecular diagnostic methods in food safety.

机构信息

Parco Tecnologico Padano, Lodi, Italy,

出版信息

Genes Nutr. 2009 Mar;4(1):1-12. doi: 10.1007/s12263-008-0106-1. Epub 2008 Dec 7.

DOI:10.1007/s12263-008-0106-1
PMID:19067016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2654054/
Abstract

Molecular methods allow the detection of pathogen nucleic acids (DNA and RNA) and, therefore, the detection of contamination in food is carried out with high selectivity and rapidity. In the last 2 decades molecular methods have accompanied traditional diagnostic methods in routine pathogen detection, and might replace them in the upcoming future. In this review the implementation in diagnostics of four of the most used molecular techniques (PCR, NASBA, microarray, LDR) are described and compared, highlighting advantages and limitations of each of them. Drawbacks of molecular methods with regard to traditional ones and the difficulties encountered in pathogen detection from food or clinical specimen are also discussed. Moreover, criteria for the choice of the target sequence for a secure detection and classification of pathogens and possible developments in molecular diagnostics are also proposed.

摘要

分子方法可用于检测病原体的核酸(DNA 和 RNA),因此,可采用高度选择性和快速的方法检测食品污染。在过去的 20 年中,分子方法已伴随传统诊断方法用于常规病原体检测,并可能在未来取代它们。本文描述并比较了最常用的四种分子技术(PCR、NASBA、微阵列、LDR)在诊断中的应用,强调了它们各自的优缺点。还讨论了分子方法相对于传统方法的缺点,以及从食品或临床标本中检测病原体时遇到的困难。此外,还提出了针对病原体安全检测和分类的靶序列选择标准,以及分子诊断的可能发展方向。