Hanon J-B, Van der Stede Y, Antonissen A, Mullender C, Tignon M, van den Berg T, Caij B
Veterinary and Agrochemical Research Centre (CODA-CERVA), Brussels, Belgium.
Transbound Emerg Dis. 2014 Apr;61(2):156-62. doi: 10.1111/tbed.12011. Epub 2012 Sep 25.
Control of bovine viral diarrhoea (BVD) in Belgium is currently implemented on a voluntary basis at herd level and mainly relies on detection and culling of persistently infected (PI) animals. The present field study was conducted during the winter of 2010/2011 to assess the performances of diagnostic assays used in the testing scheme for BVD as proposed by the two Belgian regional laboratories. Individual blood samples were collected from 4972 animals, and individual samples from the same herd were pooled (maximum of 30 individual samples per pool) and screened for the presence of Bovine Viral Diarrhoea Virus (BVDV)-specific RNA using a commercial real-time RT-PCR test (ADIAGENE). Individual samples from positive pools were then tested in parallel with the same RT-PCR test and with an antigen-capture ELISA test (IDEXX) to detect viremic animals. This study demonstrated that individual results differed according to the type of assay used (P < 0.001): 140 animals (2.8%) were positive by RT-PCR and 72 (1.4%) by antigen-ELISA. A second blood sample was taken 40 days later from 74 PCR positive animals to detect persistent viremia: 17 (23%) of these were still PCR positive and considered to be PI and the 57 that no longer tested positive were assumed to be transiently infected (TI) animals. All PI animals were positive also by antigen-ELISA at both time points. Among TI animals, 10 (16%) were positive by antigen-ELISA at the first but none at the second sampling. A highly significant difference in cycle threshold (Ct ) values obtained by RT-PCR was observed between PI and TI animals. ROC analysis was performed to establish thresholds to confirm with high probability that an animal is PI, based on the result of RT-PCR test performed on a single individual blood sample.
比利时目前在牛群层面以自愿方式实施牛病毒性腹泻(BVD)防控,主要依靠检测和扑杀持续感染(PI)动物。本现场研究于2010/2011年冬季开展,旨在评估比利时两个地区实验室提议的BVD检测方案中所使用诊断检测方法的性能。从4972头动物采集个体血样,并将同一牛群的个体样本进行合并(每个样本池最多30个个体样本),使用商业实时逆转录聚合酶链反应(RT-PCR)检测(ADIAGENE)筛查牛病毒性腹泻病毒(BVDV)特异性RNA的存在。然后,对阳性样本池中的个体样本同时使用相同的RT-PCR检测和抗原捕获酶联免疫吸附测定(ELISA)检测(IDEXX),以检测病毒血症动物。本研究表明,根据所使用检测方法的类型,个体检测结果存在差异(P < 0.001):RT-PCR检测显示140头动物(2.8%)呈阳性,抗原ELISA检测显示72头动物(1.4%)呈阳性。40天后,从74头PCR阳性动物采集第二份血样,以检测持续性病毒血症:其中17头(23%)仍为PCR阳性,被视为PI动物,另外57头不再检测为阳性的动物被假定为短暂感染(TI)动物。所有PI动物在两个时间点的抗原ELISA检测均为阳性。在TI动物中,10头(16%)在首次采样时抗原ELISA检测呈阳性,但在第二次采样时均为阴性。PI动物和TI动物通过RT-PCR获得的循环阈值(Ct)值存在高度显著差异。进行了ROC分析,以根据对单个个体血样进行RT-PCR检测的结果确定阈值,从而高概率地确认动物是否为PI。