Abstract

Nested PCR remains a labor-intensive and error-prone biomolecular analysis. Laboratory workflow automation by precise control of minute liquid volumes in centrifugal microfluidic Lab-on-a-Chip systems holds great potential for such applications. However, the majority of these systems require costly custom-made processing devices. Our idea is to augment a standard laboratory device, here a centrifugal real-time PCR thermocycler, with inbuilt liquid handling capabilities for automation. We have developed a microfluidic disk segment enabling an automated nested real-time PCR assay for identification of common European animal groups adapted to forensic standards. For the first time we utilize a novel combination of fluidic elements, including pre-storage of reagents, to automate the assay at constant rotational frequency of an off-the-shelf thermocycler. It provides a universal duplex pre-amplification of short fragments of the mitochondrial 12S rRNA and cytochrome b genes, animal-group-specific main-amplifications, and melting curve analysis for differentiation. The system was characterized with respect to assay sensitivity, specificity, risk of cross-contamination, and detection of minor components in mixtures. 92.2% of the performed tests were recognized as fluidically failure-free sample handling and used for evaluation. Altogether, augmentation of the standard real-time thermocycler with a self-contained centrifugal microfluidic disk segment resulted in an accelerated and automated analysis reducing hands-on time, and circumventing the risk of contamination associated with regular nested PCR protocols.

Highlights

  • The analysis of DNA by polymerase chain reaction (PCR) is a routinely applied method within most molecular biology laboratories, including forensic laboratories [1,2]

  • We present a centrifugal microfluidic disk segment as Microfluidic App on an off-the-shelf RGQ that automates an assay for animal family determination by nested PCR and subsequent melt curve analysis to face problems ascontamination, errorprone pipetting and higher costs of common manual workflows

  • In 94 cases (92.2%) of this study, the fluidics of the GeneSlices proved fully functional for the sample structure, disregarding the no-template control (NTC)

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Summary

Introduction

The analysis of DNA by polymerase chain reaction (PCR) is a routinely applied method within most molecular biology laboratories, including forensic laboratories [1,2]. Species or animal family determination is an important application within the field of forensic genetics mainly e.g. to ascertain animals as perpetrators or for the investigation of illegal hunting [4]. It is needed for analysis of (un-)declared ingredients within food. Restriction fragment analysis, sequencing methods, or probebased species-specific real-time PCR are applied for analyses [5,6,7,8,9]. Analysis of the PCR fragments by melt curve analysis and high resolution melting is increasing [10,11,12,13]

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