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Large scale multiplex PCR improves pathogen detection by DNA microarrays

Maria Palka-Santini1, Berit E Cleven12, Ludwig Eichinger3, Martin Krönke14 and Oleg Krut14*

Author affiliations

1 Institute for Medical Microbiology, Immunology and Hygiene, Medical Faculty, University of Cologne, Germany

2 Vulkan Technic Maschinen-Konstruktions GmbH, Germany

3 Center for Biochemistry, Medical Faculty, University of Cologne, Germany

4 Center for Molecular Medicine Cologne, Medical Center, University of Cologne, Germany

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Citation and License

BMC Microbiology 2009, 9:1  doi:10.1186/1471-2180-9-1

Published: 3 January 2009



Medium density DNA microchips that carry a collection of probes for a broad spectrum of pathogens, have the potential to be powerful tools for simultaneous species identification, detection of virulence factors and antimicrobial resistance determinants. However, their widespread use in microbiological diagnostics is limited by the problem of low pathogen numbers in clinical specimens revealing relatively low amounts of pathogen DNA.


To increase the detection power of a fluorescence-based prototype-microarray designed to identify pathogenic microorganisms involved in sepsis, we propose a large scale multiplex PCR (LSplex PCR) for amplification of several dozens of gene-segments of 9 pathogenic species. This protocol employs a large set of primer pairs, potentially able to amplify 800 different gene segments that correspond to the capture probes spotted on the microarray. The LSplex protocol is shown to selectively amplify only the gene segments corresponding to the specific pathogen present in the analyte. Application of LSplex increases the microarray detection of target templates by a factor of 100 to 1000.


Our data provide a proof of principle for the improvement of detection of pathogen DNA by microarray hybridization by using LSplex PCR.