首页> 外文期刊>Journal of Virological Methods >Differentiation between pathogenic serotype 1 isolates of Marek's disease virus and the Rispens CVI988 vaccine in Australia using real-time PCR and high resolution melt curve analysis.
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Differentiation between pathogenic serotype 1 isolates of Marek's disease virus and the Rispens CVI988 vaccine in Australia using real-time PCR and high resolution melt curve analysis.

机译:使用实时PCR和高分辨率熔解曲线分析,区分澳大利亚的马立克氏病病毒的致病血清型1分离株和Rispens CVI988疫苗。

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摘要

Two real-time PCR assays were developed which enable quantitation and differentiation between pathogenic Australian isolates of Marek's disease virus (MDV) serotype 1 and the serotype 1 vaccine strain Rispens CVI988. The assays are based on a DNA sequence variation in the meq gene between pathogenic and vaccinal MDV1 which has been confirmed by sequencing of 20 Australian field strains of MDV. Complete specificity has been demonstrated in samples containing pathogenic MDV (n=20), Rispens (3 commercial vaccine strains), or both. The limit of detection of both the Rispens-specific and the pathogenic MDV1-specific assays was 10 viral copies/reaction. The tests successfully differentiated and quantified MDV in mixtures of pathogenic and vaccinal Rispens virus. A high resolution melt curve analysis targeting the same SNP used for the real-time PCR assays was also developed which successfully detected sequence variation between Md5, six Australian MDV1 isolates and the three Rispens vaccines. However it was ineffective at differentiating mixtures of pathogenic and vaccinal MDV1. The real-time PCR assays have both diagnostic and epidemiological applications as they enable differentiation and quantitation of Rispens CVI988 and pathogenic MDV1 in co-infected chickens in Australia.
机译:已开发出两种实时PCR分析方法,可以定量分析和区分马立克氏病病毒(MDV)血清型1和血清型1疫苗菌株Rispens CVI988的澳大利亚致病菌。该测定基于致病性和疫苗性MDV1之间meq基因中的DNA序列变异,该变异已通过对20株澳大利亚MDV田间毒株进行测序而得到证实。在含有致病性MDV(n = 20),Rispens(3种商业疫苗株)或两者的样品中已证明完全特异性。 Rispens特异性和致病性MDV1特异性检测的检测极限是10个病毒拷贝/反应。该测试成功地在致病性和疫苗性的Rispens病毒混合物中区分和定量了MDV。还开发了针对实时PCR分析所用的同一SNP的高分辨率熔解曲线分析,该分析成功检测了Md5,六个澳大利亚MDV1分离株和三种Rispens疫苗之间的序列变异。但是,它在区分致病性和疫苗性MDV1混合物方面无效。实时PCR分析在诊断和流行病学方面都有应用,因为它们可以区分和定量澳大利亚共感染鸡中的Rispens CVI988和致病性MDV1。

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