Deregt Dirk, Gilbert Scott A, Dudas Sandor, Pasick John, Baxi Shailja, Burton Kimberley M, Baxi Mohit K
Virology Section, Lethbridge Laboratory, Animal Diseases Research Institute, Canadian Food Inspection Agency, Lethbridge, Alta., Canada T1J 3Z4.
J Virol Methods. 2006 Sep;136(1-2):17-23. doi: 10.1016/j.jviromet.2006.03.025. Epub 2006 May 9.
An oligonucleotide suspension microarray (Luminex microsphere system) was developed for detection and differentiation of animal pestiviruses: classical swine fever virus (CSFV), bovine viral diarrhea virus types 1 and 2 (BVDV1 and BVDV2), and border disease virus (BDV). Species-specific and pestivirus-common oligonucleotide probes were designed to the 5' UTR region and conjugated to individual color-coded Luminex carboxy beads (probe beads). Target pestivirus sequences were amplified by asymmetric PCR using a biotinylated reverse primer and a forward and reverse primer ratio of 1:5. The biotinylated products were hybridized to eight probe beads in a multiplex assay and analyzed using streptavidin conjugated to a fluorescent reporter molecule. The assay was able to detect and differentiate all 40 strains of CSFV, BVDV1, BVDV2 and BDV tested. The analytical sensitivity was determined to be 0.2-10 TCID50/ml. The major advantages of the DNA-microsphere suspension microarray, as a low density array, are its ease of handling and ability to simultaneously detect and type multiple infectious agents.
开发了一种寡核苷酸悬浮微阵列(Luminex微球系统)用于检测和区分动物瘟病毒:经典猪瘟病毒(CSFV)、1型和2型牛病毒性腹泻病毒(BVDV1和BVDV2)以及边界病病毒(BDV)。针对5'UTR区域设计了种属特异性和瘟病毒通用寡核苷酸探针,并将其与单个颜色编码的Luminex羧基微球(探针微球)偶联。使用生物素化反向引物和1:5的正向与反向引物比例,通过不对称PCR扩增目标瘟病毒序列。生物素化产物在多重检测中与八个探针微球杂交,并使用与荧光报告分子偶联的链霉亲和素进行分析。该检测方法能够检测和区分所测试的所有40株CSFV、BVDV1、BVDV2和BDV。分析灵敏度测定为0.2 - 10 TCID50/ml。作为低密度阵列的DNA - 微球悬浮微阵列的主要优点是易于操作以及能够同时检测和分型多种感染因子。