Baigent Susan J, Nair Venugopal K, Le Galludec Hervé
Avian Oncogenic Virus Group, The Pirbright Institute, Woking, GU24 0NF, United Kingdom.
Zoetis International Services, 23-25 Avenue du Docteur Lannelongue, 75668 Paris Cedex 14, France.
J Virol Methods. 2016 Jul;233:23-36. doi: 10.1016/j.jviromet.2016.03.002. Epub 2016 Mar 10.
CVI988/Rispens vaccine, the 'gold standard' vaccine against Marek's disease in poultry, is not easily distinguishable from virulent strains of Marek's disease herpesvirus (MDV). Accurate differential measurement of CVI988 and virulent MDV is commercially important to confirm successful vaccination, to diagnose Marek's disease, and to investigate causes of vaccine failure. A real-time quantitative PCR assay to distinguish CVI988 and virulent MDV based on a consistent single nucleotide polymorphism in the pp38 gene, was developed, optimised and validated using common primers to amplify both viruses, but differential detection of PCR products using two short probes specific for either CVI988 or virulent MDV. Both probes showed perfect specificity for three commercial preparations of CVI988 and 12 virulent MDV strains. Validation against BAC-sequence-specific and US2-sequence-specific q-PCR, on spleen samples from experimental chickens co-infected with BAC-cloned pCVI988 and wild-type virulent MDV, demonstrated that CVI988 and virulent MDV could be quantified very accurately. The assay was then used to follow kinetics of replication of commercial CVI988 and virulent MDV in feather tips and blood of vaccinated and challenged experimental chickens. The assay is a great improvement in enabling accurate differential quantification of CVI988 and virulent MDV over a biologically relevant range of virus levels.
CVI988/Rispens疫苗是预防家禽马立克氏病的“金标准”疫苗,它与马立克氏病疱疹病毒(MDV)的强毒株不易区分。准确区分CVI988和强毒株MDV在商业上具有重要意义,可用于确认疫苗接种是否成功、诊断马立克氏病以及调查疫苗失效的原因。基于pp38基因中一个一致的单核苷酸多态性,开发、优化并验证了一种实时定量PCR检测方法,该方法使用通用引物扩增两种病毒,但使用两种分别针对CVI988或强毒株MDV的短探针进行PCR产物的差异检测。两种探针对三种CVI988商业制剂和12种强毒株MDV均表现出完美的特异性。对同时感染BAC克隆的pCVI988和野生型强毒株MDV的实验鸡脾脏样本进行BAC序列特异性和US2序列特异性q-PCR验证,结果表明CVI988和强毒株MDV能够被非常准确地定量。然后该检测方法被用于追踪商业CVI988和强毒株MDV在接种疫苗和攻毒的实验鸡羽毛尖端和血液中的复制动力学。与在生物学相关病毒水平范围内准确区分CVI988和强毒株MDV的现有方法相比,该检测方法有了很大改进。