Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany.
PLoS One. 2012;7(6):e38251. doi: 10.1371/journal.pone.0038251. Epub 2012 Jun 29.
Porcine reproductive and respiratory syndrome (PRRS) causes economic losses in the pig industry worldwide, and PRRS viruses (PRRSV) are classified into the two distinct genotypes "North American (NA, type 2)" and "European (EU, type 1)". In 2006, a highly pathogenic NA strain of PRRSV (HP-PRRSV), characterized by high fever as well as high morbidity and mortality, emerged in swine farms in China. Therefore, a real-time reverse transcription polymerase chain reaction (RT-qPCR) assay specific for HP-PRRSV was developed and combined with type 1- and type 2-specific RT-qPCR systems. Furthermore, an internal control, based on a heterologous RNA, was successfully introduced. This final multiplex PRRSV RT-qPCR, detecting and typing PRRSV, had an analytical sensitivity of less than 200 copies per µl for the type 1-assay and 20 copies per µl for the type 2- and HP assays and a high diagnostic sensitivity. A panel of reference strains and field isolates was reliably detected and samples from an animal trial with a Chinese HP-PRRS strain were used for test validation. The new multiplex PRRSV RT-qPCR system allows for the first time the highly sensitive detection and rapid differentiation of PRRSV of both genotypes as well as the direct detection of HP-PRRSV.
猪繁殖与呼吸综合征(PRRS)在全球范围内给养猪业造成了经济损失,PRRS 病毒(PRRSV)分为两个截然不同的基因型“北美(NA,型 2)”和“欧洲(EU,型 1)”。2006 年,中国猪场出现了一种高致病性的 NA 株 PRRSV(HP-PRRSV),其特征为高热以及高发病率和死亡率。因此,开发了一种针对 HP-PRRSV 的实时逆转录聚合酶链反应(RT-qPCR)检测方法,并与 1 型和 2 型特异性 RT-qPCR 系统相结合。此外,还成功引入了基于异源 RNA 的内部对照。这种最终的多重 PRRSV RT-qPCR 检测和分型 PRRSV 的方法,对于 1 型检测的分析灵敏度低于 200 拷贝/µl,对于 2 型和 HP 检测的分析灵敏度低于 20 拷贝/µl,具有很高的诊断灵敏度。参考株和田间分离株的检测结果可靠,并用中国 HP-PRRS 株进行的动物试验样本进行了验证。该新型多重 PRRSV RT-qPCR 系统首次实现了对两种基因型 PRRSV 的高灵敏度检测和快速区分,以及 HP-PRRSV 的直接检测。