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利用实时聚合酶链反应对田间灰尘样本、羽毛尖端和脾脏中的2型马立克氏病病毒进行绝对定量分析。

Absolute quantification using real-time polymerase chain reaction of Marek's disease virus serotype 2 in field dust samples, feather tips and spleens.

作者信息

Renz Katrin G, Islam Aminul, Cheetham Brian F, Walkden-Brown Stephen W

机构信息

Centre for Animal Health and Welfare, School of Rural Science and Agriculture, University of New England, Armidale, NSW 2351, Australia.

出版信息

J Virol Methods. 2006 Aug;135(2):186-91. doi: 10.1016/j.jviromet.2006.03.017. Epub 2006 May 6.

Abstract

Methods for Taqman quantitative real-time PCR (qPCR) assays to detect the three serotypes of Marek's disease virus (MDV) are available, and absolute quantification has been developed for MDV serotype 1 and serotype 3. The development of a method for absolute quantification of Marek's disease virus serotype 2 (MDV2) is described in this paper. Using plasmid DNA, the lower detection limit of the MDV2 assay was determined to be 10 copies. Three independent assay runs showed highly reproducible Ct values and calculated copy numbers, with mean intra- and inter-assay coefficients of variation of less than 3% for Ct and less than 21.5% for calculated copy number. Absolute quantification of MDV2 was performed successfully on dust samples collected from poultry farms across Australia, material from infectious spleens and feather tips from chickens vaccinated with an attenuated strain of MDV2. Thus, it is now possible to use qPCR assays for absolute quantification of all three serotypes of MDV in a sample.

摘要

检测马立克氏病病毒(MDV)三种血清型的Taqman定量实时聚合酶链反应(qPCR)检测方法已经存在,并且已经开发出针对MDV1型和3型的绝对定量方法。本文描述了一种用于马立克氏病病毒2型(MDV2)绝对定量方法的开发。使用质粒DNA,确定MDV2检测的下限为10个拷贝。三次独立的检测运行显示出高度可重复的Ct值和计算出的拷贝数,Ct值的平均批内和批间变异系数小于3%,计算出的拷贝数变异系数小于21.5%。对从澳大利亚各地家禽养殖场采集的灰尘样本、感染脾脏的材料以及接种MDV2减毒株的鸡的羽毛尖端成功进行了MDV2的绝对定量。因此,现在可以使用qPCR检测对样本中MDV的所有三种血清型进行绝对定量。

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