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利用实时逆转录聚合酶链反应(RT-PCR)快速检测和鉴定猪繁殖与呼吸综合征病毒(PRRSV)

Rapid detection and strain identification of porcine reproductive and respiratory syndrome virus (PRRSV) by real-time RT-PCR.

作者信息

Lurchachaiwong W, Payungporn S, Srisatidnarakul U, Mungkundar C, Theamboonlers A, Poovorawan Y

机构信息

Center of Excellence in Clinical Virology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

Lett Appl Microbiol. 2008 Jan;46(1):55-60. doi: 10.1111/j.1472-765X.2007.02259.x. Epub 2007 Oct 15.

Abstract

AIMS

To develop and validate assays based on real-time reverse transcriptase-polymerase chain reaction (RT-PCR) for rapid detection and strain identification (European and North American strains) of porcine reproductive and respiratory syndrome virus (PRRSV) by using SYBR Green I and TaqMan probe chemistries.

METHODS AND RESULTS

This study describes two alternative assays based on real-time RT-PCR for rapid detection and strain identification of PRRSV in comparison with conventional RT-PCR. The first assay utilized SYBR Green I with melting curve analysis; another assay was performed using strain-specific TaqMan probes. Primers were selected from the conserved regions within ORF7 (N) of both strains whereas two TaqMan probes labelled with different fluorescent dyes were specifically designed for each strain. The result of strain identification was confirmed by direct sequencing. Both assays can be used for rapid detection and strain identification of PRRSV with a sensitivity of 10(4) and 10(3) copies microl(-1) for SYBR Green and TaqMan probe, respectively.

CONCLUSIONS

Real-time RT-PCR is a powerful method combining rapidity, specificity and efficiency for large-scale screening and strain identification of PRRSV.

SIGNIFICANCE AND IMPACT OF THE STUDY

The data indicate that the methods developed are invaluable for detecting low levels of PRRSV infection in swine.

摘要

目的

开发并验证基于实时逆转录聚合酶链反应(RT-PCR)的检测方法,利用SYBR Green I和TaqMan探针技术,快速检测猪繁殖与呼吸综合征病毒(PRRSV)并进行毒株鉴定(欧洲株和北美株)。

方法与结果

本研究描述了两种基于实时RT-PCR的替代检测方法,用于快速检测PRRSV并与传统RT-PCR进行毒株鉴定比较。第一种检测方法利用SYBR Green I结合熔解曲线分析;另一种检测方法使用毒株特异性TaqMan探针。引物从两种毒株的开放阅读框7(N)保守区域中选取,而两种分别标记不同荧光染料的TaqMan探针则针对每种毒株专门设计。毒株鉴定结果通过直接测序确认。两种检测方法均可用于PRRSV的快速检测和毒株鉴定,SYBR Green和TaqMan探针检测的灵敏度分别为10(4)和10(3)拷贝微升(-1)。

结论

实时RT-PCR是一种强大的方法,结合了快速性、特异性和高效性,可用于PRRSV的大规模筛查和毒株鉴定。

研究的意义与影响

数据表明所开发的方法对于检测猪中低水平的PRRSV感染具有重要价值。

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