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一种用于从羽毛尖端检测致癌性马立克氏病病毒的巢式聚合酶链反应方法的开发。

Development of a nested polymerase chain reaction method to detect oncogenic Marek's disease virus from feather tips.

作者信息

Murata Shiro, Chang Kyung-Soo, Lee Sung-Il, Konnai Satoru, Onuma Misao, Ohashi Kazuhiko

机构信息

Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan.

出版信息

J Vet Diagn Invest. 2007 Sep;19(5):471-8. doi: 10.1177/104063870701900503.

Abstract

For the easy survey of Marek's disease virus (MDV), feather tip-derived DNA from MDV-infected chickens can be used because feather tips are easy to collect and feather follicle epithelium is known to be the only site of productive replication of cell-free MDV. To develop a diagnostic method to differentiate highly virulent strains of MDV from the attenuated MDV vaccine strain, CVI988, which is widely used, nested polymerase chain reaction (PCR) was performed to detect a segment of the meq gene in feather tip samples of chickens experimentally infected with MDV. In chickens infected with Md5, a strain of oncogenic MDV, the meq gene was consistently detected, whereas the L-meq gene, in which a 180-base pair (180-bp) sequence is inserted into the meq gene, was detected in CVI988-infected chickens. Moreover, the meq gene was mainly detected even in chickens co-infected with both Md5 and CVI988. These results suggest that this method is appropriate for the surveillance of the highly virulent MDV infection in the field.

摘要

为便于对马立克氏病病毒(MDV)进行检测,可使用来自感染MDV的鸡的羽尖DNA,因为羽尖易于采集,且已知毛囊上皮是无细胞MDV进行有效复制的唯一部位。为开发一种诊断方法,以区分MDV的高毒株和广泛使用的减毒MDV疫苗株CVI988,采用巢式聚合酶链反应(PCR)检测经MDV实验感染的鸡羽尖样本中的meq基因片段。在感染致癌性MDV毒株Md5的鸡中,可始终检测到meq基因,而在感染CVI988的鸡中,检测到L-meq基因,该基因在meq基因中插入了一段180个碱基对(180-bp)的序列。此外,即使在同时感染Md5和CVI988的鸡中,也主要检测到meq基因。这些结果表明,该方法适用于现场高致病性MDV感染的监测。

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