Differential quantification of cloned CVI988 vaccine strain and virulent RB-1B strain of Marek's disease viruses in chicken tissues, using real-time PCR

被引:32
作者
Baigent, S. J. [1 ]
Smith, L. P. [1 ]
Petherbridge, L. J. [1 ]
Nair, V. K. [1 ]
机构
[1] Inst Anim Hlth, Avian Oncogen Virus Grp, Newbury RG20 7NN, Berks, England
基金
英国生物技术与生命科学研究理事会;
关键词
Marek's disease virus; Vaccination; CVI988/Rispens; Real-time PCR; Bacterial-artificial-chromosome; POLYMERASE-CHAIN-REACTION; BACTERIAL ARTIFICIAL CHROMOSOMES; FEATHER TIPS; ABSOLUTE QUANTITATION; INFECTED CHICKENS; DUST SAMPLES; HERPESVIRUS; PROTECTION; PATHOGENESIS; REPLICATION;
D O I
10.1016/j.rvsc.2010.08.002
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The 'gold standard' vaccine against Marek's disease in poultry is the CVI988/Rispens virus, which is not easily distinguishable, antigenically or genetically, from virulent Marek's disease herpesvirus. Accurate differential measurement of the CVI988 vaccine and virulent viruses is important to investigate mechanisms of vaccinal protection. Minimal sequence differences between CVI988 and virulent MDV strains restrict the application of molecular diagnostic methods such as real-time PCR to distinguish between these viruses. The use of bacterial-artificial-chromosome (BAC) cloned CVI988 virus, which carries the BAC vector sequences in place of the U(s)2 gene, allows its differential quantification from virulent strains using real-time PCR assays that target the BAC vector sequence and the U(s)2 gene respectively. These novel assays allowed investigation of replication of both serotype-1 vaccine virus (cloned CVI988) and challenge virus (RB-1B strain) in tissues of individual chickens in an experimental vaccination-challenge model of Marek's disease. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:167 / 174
页数:8
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