Dénes Lilla, Horváth Dávid G, Duran Oliver, Ratkhjen Poul H, Kraft Christian, Acs Balazs, Szász Attila M, Rümenapf Till, Papp Marton, Ladinig Andrea, Balka Gyula
Department of Pathology, University of Veterinary Medicine, István u. 2, 1078 Budapest, Hungary.
Boehringer Ingelheim Vetmedica GmbH, 55218 Ingelheim am Rhein, Germany.
Vet Sci. 2021 Oct 15;8(10):235. doi: 10.3390/vetsci8100235.
and are the causative agents of porcine reproductive and respiratory syndrome (PRRS), which is one of the most significant diseases of the swine industry, causing significant economic losses in the main pig producing countries. Here, we report the development of a novel, RNA-based in situ hybridization technique (RNAscope) to detect PRRS virus (PRRSV) RNA in lung tissues of experimentally infected animals. The technique was applied to lung tissues of 20 piglets, which had been inoculated with a wild-type, highly pathogenic PRRSV-1 strain. To determine the RNAscope's applicability as a semi-quantitative method, we analysed the association between the proportion of the virus-infected cells measured with an image analysis software (QuPath) and the outcome of the real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) tests performed in parallel. The results of the quantitative approach of these two molecular biological methods show significant association (pseudo R = 0.3894, = 0.004). This is the first time RNAscope assay has been implemented for the detection of PRRSV-1 in experimental animals.
[病毒名称1]和[病毒名称2]是猪繁殖与呼吸综合征(PRRS)的病原体,PRRS是养猪业中最重要的疾病之一,在主要生猪生产国造成了重大经济损失。在此,我们报告了一种新型的基于RNA的原位杂交技术(RNAscope)的开发,用于检测实验感染动物肺组织中的PRRS病毒(PRRSV)RNA。该技术应用于20只仔猪的肺组织,这些仔猪接种了野生型高致病性PRRSV-1毒株。为了确定RNAscope作为一种半定量方法的适用性,我们分析了用图像分析软件(QuPath)测量的病毒感染细胞比例与同时进行的实时定量逆转录聚合酶链反应(qRT-PCR)测试结果之间的关联。这两种分子生物学方法的定量方法结果显示出显著关联(伪R = 0.3894,P = 0.004)。这是首次在实验动物中应用RNAscope检测法检测PRRSV-1。