用于检测病原体的低密度 TaqMan® 阵列卡。

4区 生物学 Q2 Medicine
Methods in Microbiology Pub Date : 2015-01-01 Epub Date: 2015-08-03 DOI:10.1016/bs.mim.2015.06.002
Jude Heaney, Kathryn Rolfe, Nicholas S Gleadall, Jane S Greatorex, Martin D Curran
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引用次数: 0

摘要

在过去的 15 年或更长的时间里,实时 PCR 检测技术彻底改变了微生物诊断技术。随着时间的推移,经过调整和改进,开发出了多重检测方法。然而,由于可用荧光基团的限制,可组合的检测数量仍然是个位数。后一种限制导致人们倾向于关注单个病原体及其检测。本章将介绍 TaqMan® 阵列卡 (TAC) 的开发过程,该技术可利用小容量和实时 PCR 从单个核酸提取物中检测多种病原体(最多 48 个目标)。这反过来又为传染病的综合症诊断提供了可能。我们以自己的实验室和其他实验室开发的 TAC 为例,介绍了针对呼吸道、胃肠道和肝脏感染的 TAC 的设计、优化和使用。我们还讨论了个别检测方法的改进以及在阵列卡中加入适当的内部控制和过程控制的问题。最后,还举例说明了这些检测方法对患者护理产生的直接、积极影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-Density TaqMan® Array Cards for the Detection of Pathogens.

Real-time PCR assays have revolutionised diagnostic microbiology over the past 15 years or more. Adaptations and improvements over that time frame have led to the development of multiplex assays. However, limitations in terms of available fluorophores has meant the number of assays which can be combined has remained in single figures. This latter limitation has led to the focus tending to be on individual pathogens and their detection. This chapter describes the development of TaqMan® Array Cards (TACs), technology which allows the detection of multiple pathogens (up to 48 targets) from a single nucleic acid extract, utilising small volumes and real-time PCR. This in turn lends itself to a syndromic approach to infectious disease diagnosis. Using the examples of TACs we have developed in our own laboratory, as well as others, we explain the design, optimisation and use of TACs for respiratory, gastrointestinal and liver infections. Refinement of individual assays is discussed as well as the incorporation of appropriate internal and process controls onto the array cards. Finally, specific examples are given of instances where the assays have had a direct, positive impact on patient care.

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来源期刊
Methods in Microbiology
Methods in Microbiology 生物-生化研究方法
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
>12 weeks
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