Development of a primer-probe energy transfer based real-time PCR for detection of Marek's disease virus

被引:4
作者
Barfoed, Annette Malene [1 ]
Ostergaard, Erik
Frandsen, Peer Lyng
Nielsen, Eva Baekdahl
Sandberg, Eva
Rasmussen, Thomas Bruun [2 ]
机构
[1] Danish Med Agcy, Med Control Div, DK-2300 Copenhagen S, Denmark
[2] Tech Univ Denmark, DTU Natl Vet Inst, DK-4771 Kalvehave, Denmark
关键词
Marek's disease virus; Real-time PCR; Primer-probe energy transfer; POLYMERASE-CHAIN-REACTION; HORIZONTAL SPREAD; SEQUENCE-ANALYSIS; GENOME; ASSAY; HERPESVIRUS; FEATHER; QUANTITATION; SEROTYPES; REGIONS;
D O I
10.1016/j.jviromet.2009.12.012
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
A real-time PCR assay, which enables simultaneous detection and differentiation of all three serotypes of Marek's disease virus, without the need for post-PCR sequencing, has been developed. The assay is based on the primer-probe energy transfer real-time PCR, which has a relatively high tolerance towards point mutations in the probe region. The PCR is followed by a probe melting point analysis, which enables confirmation of identity of amplicon and differentiation of serotypes. The assay targets the MDV031 gene, encoding UL19 major capsid protein-like protein and was shown to be quantitative, with a detection limit below 10 TCID50/ml starting material. This sensitivity is similar to the one obtained with traditional virus cultivation. However, the PCR method can provide a laboratory result within a day, while the virus cultivation method takes more than a week to perform. The new method will be useful for testing of avian live viral vaccines and screening for extraneous agents. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:21 / 26
页数:6
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