Finlaison D S, Read A J, Zhang J, Paskin R, Kirkland P D
Virology Laboratory, Elizabeth Macarthur Agriculture Institute, Department of Primary Industries, Private Bag 4008, Narellan, New South Wales, 2567, Australia.
Aust Vet J. 2014 Jan;92(1-2):24-7. doi: 10.1111/avj.12139.
To report the occurrence of an epizootic of bovine ephemeral fever (BEF) in New South Wales (NSW) and northern Victoria in 2009-10 and describe the application of a real-time reverse transcription polymerase chain reaction (qRT-PCR) assay during the outbreak.
Whole-blood samples from animals exhibiting clinical signs of BEF were requested from district veterinarians in NSW. In addition, samples were submitted from private practitioners in NSW and Victoria. In NSW, samples from animals showing acute clinical signs of BEF were tested using a qRT-PCR assay. Serological testing for BEF diagnosis was undertaken as required. Virus isolation was performed on selected samples in which bovine ephemeral fever virus (BEFV) RNA was detected. Archival serum samples and mosquito homogenates were also tested for BEFV by qRT-PCR.
Accessions were received from 121 properties in NSW, with cases of BEF confirmed on 84 properties by qRT-PCR and 20 properties by serology. In northern Victoria, BEF was confirmed on 25 properties based on serological testing. Screening of samples by qRT-PCR enhanced the success of BEFV isolation. BEFV RNA was successfully detected in archival serum samples and a single mosquito homogenate.
The 2009-10 outbreak resulted in the most extensive transmission of BEFV in NSW and Victoria since 1995-96, and follows a smaller outbreak in summer-autumn 2008. The use of qRT-PCR for BEF diagnosis offers veterinarians and cattle owners rapid confirmation of infection (1-2 days) and provides 'real-time' information about the presence of the disease in a district.
报告2009 - 10年新南威尔士州(NSW)和维多利亚州北部牛流行热(BEF)的 epizootic 发生情况,并描述疫情爆发期间实时逆转录聚合酶链反应(qRT-PCR)检测方法的应用。
向新南威尔士州的地区兽医索要表现出牛流行热临床症状的动物的全血样本。此外,新南威尔士州和维多利亚州的私人执业者也提交了样本。在新南威尔士州,对表现出牛流行热急性临床症状的动物样本使用qRT-PCR检测方法进行检测。根据需要进行牛流行热诊断的血清学检测。对检测出牛流行热病毒(BEFV)RNA的选定样本进行病毒分离。还通过qRT-PCR对存档血清样本和蚊虫匀浆进行牛流行热病毒检测。
收到来自新南威尔士州121个养殖场的样本,通过qRT-PCR在84个养殖场确诊牛流行热病例,通过血清学在20个养殖场确诊。在维多利亚州北部,根据血清学检测在25个养殖场确诊牛流行热。通过qRT-PCR对样本进行筛查提高了牛流行热病毒分离的成功率。在存档血清样本和单个蚊虫匀浆中成功检测到牛流行热病毒RNA。
2009 - 10年的疫情爆发导致牛流行热病毒自1995 - 96年以来在新南威尔士州和维多利亚州传播最为广泛,此前在2008年夏秋季节有一次规模较小的疫情爆发。使用qRT-PCR进行牛流行热诊断可为兽医和养牛户提供感染的快速确认(1 - 2天),并提供有关该地区疾病存在情况的“实时”信息。