Division of Microbiology, Department of Pathology and Laboratory Medicine, Capital District Health Authority, Room 404B, Mackenzie Building, 5788 University Ave, Halifax NS B3H 1V8, Canada.
Virol J. 2013 Jun 7;10:184. doi: 10.1186/1743-422X-10-184.
Compared to traditional testing strategies, nucleic acid amplification tests such as real-time PCR offer many advantages for the detection of human adenoviruses. However, commercial assays are expensive and cost prohibitive for many clinical laboratories. To overcome fiscal challenges, a cost effective strategy was developed using a combination of homogenization and heat treatment with an "in-house" real-time PCR. In 196 swabs submitted for adenovirus detection, this crude extraction method showed performance characteristics equivalent to viral DNA obtained from a commercial nucleic acid extraction. In addition, the in-house real-time PCR outperformed traditional testing strategies using virus culture, with sensitivities of 100% and 69.2%, respectively. Overall, the combination of homogenization and heat treatment with a sensitive in-house real-time PCR provides accurate results at a cost comparable to viral culture.
与传统的检测策略相比,核酸扩增检测(如实时 PCR)在检测人类腺病毒方面具有许多优势。然而,对于许多临床实验室来说,商业检测方法昂贵且难以承受。为了克服财政挑战,采用了一种经济有效的策略,使用均质化和热处理与“内部”实时 PCR 相结合。在 196 个提交用于腺病毒检测的拭子中,这种粗提取方法显示出与从商业核酸提取获得的病毒 DNA 相当的性能特征。此外,内部实时 PCR 的性能优于使用病毒培养的传统检测策略,其灵敏度分别为 100%和 69.2%。总的来说,使用敏感的内部实时 PCR 进行均质化和热处理的组合可提供准确的结果,成本与病毒培养相当。