Tabrizi Sepehr N, Stevens Matthew, Chen Shujun, Rudland Elice, Kornegay Janet R, Garland Suzanne M
Department of Molecular Microbiology, Microbiology and Infectious Diseases, the Royal Women's Hospital, Victoria, Australia.
Am J Clin Pathol. 2005 Jun;123(6):896-9. doi: 10.1309/MPER-NJ0G-62RE-CHCQ.
Detection and typing of human papillomaviruses (HPVs) are requested by clinicians with growing frequency as part of the overall management of patients. A new method using consensus L1 amplification and a reverse line blot hybridization detection method has been described for broad spectrum HPV genotype identification. This method involves hybridization at 53 degrees C in a shaking water bath, which many laboratories might find cumbersome. We describe a modified hybridization step, using a dry-air incubator, that simplifies the detection protocol. Overall, comparable results were obtained by the modified, more easily performed protocol, indicating that laboratories might validate and use this modified method.
随着对患者进行全面管理的一部分,临床医生对人乳头瘤病毒(HPV)检测和分型的需求日益增加。一种使用共识L1扩增和反向线印迹杂交检测方法的新方法已被描述用于广谱HPV基因型鉴定。该方法涉及在53摄氏度的振荡水浴中进行杂交,许多实验室可能会觉得这很麻烦。我们描述了一种使用干空气培养箱的改良杂交步骤,简化了检测方案。总体而言,通过改良的、更易于操作的方案获得了可比的结果,这表明实验室可以验证并使用这种改良方法。