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Optimized MOL-PCR for Characterization of Microbial Pathogens

Wuyts, Véronique
Bertrand, Sophie
Marchal, Kathleen
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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.

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2016-01-06
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Peer reviewed scientific article
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bacteria, Biomarkers, Biotinylation, DNA, Bacterial, Electrophoresis, Gel, Pulsed-Field, Fluorescent Dyes, Genetic Markers, Humans, Nucleic Acid Hybridization, Oligonucleotide Probes, Phycoerythrin, polymerase chain reaction, Polymorphism, Single Nucleotide, Salmonella typhimurium, Streptavidin, Temperature
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