Pabbaraju Kanti, Wong Sallene, Fox Julie D
Provincial Laboratory for Public Health and University of Calgary, Calgary, AB, Canada.
Methods Mol Biol. 2011;665:1-15. doi: 10.1007/978-1-60761-817-1_1.
The human adenovirus (hAdV) group is represented by 52 serotypes that have been reported to cause a broad range of clinical manifestations including respiratory tract infections, acute conjunctivitis, cystitis, gastroenteritis, and systemic infections. Conventional methods for detection of hAdVs include electron microscopy, antigen detection, and virus isolation in cell culture. Implementation of real-time PCR assays has increased the sensitivity and speed of detection, and allowed for rapid quantification and serotyping. This chapter describes the design and validation of a multiplex real-time PCR assay for the detection of a broad range of hAdV serotypes in respiratory samples, blood, or urine. This assay targets the conserved region of the hAdV hexon gene and utilizes hydrolysis probes for the detection of amplified products. The assay can be adapted to provide quantitative results to evaluate the change in viral load, and products can be sequenced for serotype designation. PCR-based methods for hAdV detection are sensitive, specific, allow for rapid diagnosis, and facilitate epidemiological studies.
人腺病毒(hAdV)组由52种血清型代表,据报道可引起广泛的临床表现,包括呼吸道感染、急性结膜炎、膀胱炎、肠胃炎和全身感染。检测hAdV的传统方法包括电子显微镜检查、抗原检测和细胞培养中的病毒分离。实时PCR检测方法的应用提高了检测的灵敏度和速度,并实现了快速定量和血清分型。本章描述了一种多重实时PCR检测方法的设计和验证,该方法用于检测呼吸道样本、血液或尿液中的多种hAdV血清型。该检测方法靶向hAdV六邻体基因的保守区域,并利用水解探针检测扩增产物。该检测方法可用于提供定量结果以评估病毒载量的变化,并且产物可进行测序以确定血清型。基于PCR的hAdV检测方法灵敏、特异,可实现快速诊断,并有助于流行病学研究。