Véronique Wuyts, Nancy H.C. Roosens, Sophie Bertrand, Kathleen Marchal, Sigrid C.J. De Keersmaecker
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Abstract
Characterization of microbial pathogens is necessary for surveillance, outbreak detection, and tracing of outbreak sources. This unit describes a multiplex oligonucleotide ligation-PCR (MOL-PCR) optimized for characterization of microbial pathogens. With MOL-PCR, different types of markers, like unique sequences, single-nucleotide polymorphisms (SNPs) and indels, can be simultaneously analyzed in one assay. This assay consists of a multiplex ligation for detection of the markers, a singleplex PCR for signal amplification, and hybridization to MagPlex-TAG beads for readout on a Luminex platform after fluorescent staining. The current protocol describes the MOL-PCR, as well as methods for DNA isolation, probe design, and data interpretation and it is based on an optimized MOL-PCR assay for subtyping of Salmonella Typhimurium. © 2016 by John Wiley & Sons, Inc.
优化的MOL-PCR鉴定微生物病原菌
微生物病原体的特征对于监测、疫情检测和追踪疫情来源是必要的。本单元描述了一个多重寡核苷酸连接pcr (MOL-PCR)优化表征微生物病原体。使用MOL-PCR,可以在一次检测中同时分析不同类型的标记,如独特序列、单核苷酸多态性(SNPs)和indel。该检测包括用于检测标记物的多重连接,用于信号扩增的单路PCR,以及荧光染色后在Luminex平台上与MagPlex-TAG珠杂交以读出。目前的方案描述了MOL-PCR,以及DNA分离、探针设计和数据解释的方法,它是基于优化的鼠伤寒沙门菌分型的MOL-PCR测定。©2016 by John Wiley &儿子,Inc。
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