Sellers Holly S, Koci Matthew D, Linnemann Erich, Kelley Laura A, Schultz-Cherry Stacey
Department of Avian Medicine, College of Veterinary Medicine, University of Georgia, Athens, GA 30602, USA.
Avian Dis. 2004 Sep;48(3):531-9. doi: 10.1637/7128.
A multiplex reverse transcription-polymerase chain reaction (RT-PCR) assay was developed for the simultaneous detection of two enteric viruses of poultry: turkey enteric coronavirus (TCV) and turkey astrovirus (TAstV). PCR primers were designed to conserved regions within the nucleocapsid gene of TCV and to the polymerase gene of TAstV-2. The primer pairs were successfully used in a multiplex RT-PCR to detect nucleic acid of TAstV-2 and TCV. The test was optimized for use with intestines/feces from naturally infected turkeys. The primers were specific and did not amplify other common RNA or DNA avian viruses. The detection limit was determined to be 10 ng of RNA used as starting template. The use of this specific test allows the rapid and early diagnosis of two financially costly viruses affecting the commercial turkey industry.
开发了一种多重逆转录-聚合酶链反应(RT-PCR)检测方法,用于同时检测家禽的两种肠道病毒:火鸡肠道冠状病毒(TCV)和火鸡星状病毒(TAstV)。PCR引物针对TCV核衣壳基因内的保守区域以及TAstV-2的聚合酶基因进行设计。这些引物对成功用于多重RT-PCR,以检测TAstV-2和TCV的核酸。该检测方法针对自然感染火鸡的肠道/粪便进行了优化。这些引物具有特异性,不会扩增其他常见的禽类RNA或DNA病毒。检测限确定为用作起始模板的10 ng RNA。这种特异性检测方法的使用能够快速早期诊断影响商业火鸡产业的两种造成巨大经济损失的病毒。