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一种用于从病毒拭子中检测腺病毒的具有成本效益的实时 PCR 方法。

A cost effective real-time PCR for the detection of adenovirus from viral swabs.

机构信息

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.

出版信息

Virol J. 2013 Jun 7;10:184. doi: 10.1186/1743-422X-10-184.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cbc/3679997/53f7a651a1a7/1743-422X-10-184-1.jpg

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