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Development of a real-time RT-PCR assay with TaqMan probe for specific detection of acute bee paralysis virus.

Abstract：

:Real-time polymerase chain reaction (real-time PCR) is an accurate, rapid and reliable method that can be used for the detection and also for the quantitation of specific DNA molecules. It can be non-specific, with intercalating dyes (SYBR Green I dye) able to bind to any dsDNA, or specific with a probe (TaqMan), whereby the probe is designed to bind within the amplified PCR fragment. A new real-time reverse transcription and polymerase chain reaction (real time RT-PCR) assay with TaqMan probe for specific detection of acute bee paralysis virus was designed. The assay was optimized to be highly sensitive and analytically specific and tested with a selection of genetically diverse ABPV strains originating from Slovenia, the United Kingdom (UK), Hungary and Germany. The detection limit of the assay and sensitivity comparisons with conventional RT-PCR were analyzed and this assay can detect a minimum of 44 copies of ABPV/reaction and is 230 times more sensitive than conventional RT-PCR. In addition, the assay is highly reproducible, with an average slope of standard curve made of ten-fold dilutions of standard copies/reaction -3.479±0.19 and an average slope of standard curve made of ten-fold dilutions of RNA -3.409±0.18.

journal_name

J Virol Methods

journal_title

Journal of virological methods

authors

Jamnikar Ciglenečki U,Toplak I

doi

10.1016/j.jviromet.2012.05.010

subject

Has Abstract

pub_date

2012-09-01 00:00:00

pages

63-8

issue

1-2

eissn

0166-0934

issn

1879-0984

pii

S0166-0934(12)00166-8

journal_volume

184

pub_type

杂志文章

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