Research Program Infection and Cancer, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 242, Heidelberg, Germany.
J Virol Methods. 2010 Dec;170(1-2):67-72. doi: 10.1016/j.jviromet.2010.08.020. Epub 2010 Sep 15.
Bovine papillomaviruses (BPV) induce benign tumours of the cutaneous or mucosal epithelia in cattle, but are also involved in the development of cancer of the urinary bladder and of the upper gastrointestinal tract. Current BPV genotyping assays employ techniques developed originally for the detection of human papillomaviruses. These methods rely on consensus PCR amplification and subsequent sequencing and are cumbersome and limited in their analytic sensitivity to detect BPV, especially in multiple infections. In this study, a novel multiplex BPV genotyping assay is described to detect sensitively and specifically BPV-1 to -10 as well as BaPV-11. The assay is based on a multiplex PCR using novel broad-spectrum bovine papillomavirus (BSBP) primers followed by multiplex bovine genotyping (MBG) by Luminex xMAP technology. The detection limit of the assay was shown to be between 10 and 100 BPV genomes. In a first application, BPV was detected in 100% of wart preparations with BPV-8 being most prevalent, followed by types 6, 1 and 10. The majority of warts were positive for at least four BPV types. In conclusion, BSBP-PCR/MBG is a powerful high-throughput method suitable for the study of the natural history of BPV and could be useful to veterinarians for the monitoring of the efficacy of future BPV vaccines.
牛乳头瘤病毒 (BPV) 会在牛的皮肤或黏膜上皮引起良性肿瘤,但也与膀胱癌和上消化道癌症的发展有关。目前的 BPV 基因分型检测方法采用最初为检测人乳头瘤病毒而开发的技术。这些方法依赖于共识 PCR 扩增,然后进行测序,繁琐且在分析灵敏度上有限,难以检测 BPV,尤其是在多重感染的情况下。在这项研究中,描述了一种新的多重 BPV 基因分型检测方法,以灵敏和特异地检测 BPV-1 到 -10 以及 BaPV-11。该检测方法基于使用新型广谱牛乳头瘤病毒 (BSBP) 引物的多重 PCR,然后通过 Luminex xMAP 技术进行多重牛基因分型 (MBG)。该检测方法的检测限被证明在 10 到 100 个 BPV 基因组之间。在首次应用中,在 100%的疣制剂中检测到 BPV,其中 BPV-8 最为普遍,其次是 6、1 和 10 型。大多数疣至少对四种 BPV 类型呈阳性。总之,BSBP-PCR/MBG 是一种强大的高通量方法,适用于研究 BPV 的自然史,并且对兽医监测未来 BPV 疫苗的效果可能有用。