Research Article: Set-up and validation of mycobacterial interspersed repetitive unit-variable number of tandem repeat (MIRU-VNTR) analysis of Mycobacterium tuberculosis using BioNumerics software

Date Published: October 31, 2018

Publisher: Public Library of Science

Author(s): Mathias Klok Pedersen, Aase Bengaard Andersen, Dorte Bek Folkvardsen, Erik Michael Rasmussen, Erik Svensson, Troels Lillebaek, Philip Supply, Olivier Neyrolles.

http://doi.org/10.1371/journal.pone.0205336

Abstract

The objective was to describe and validate a new and alternative software procedure for 24-locus mycobacterial interspersed repetitive unit-variable number-tandem repeat (MIRU-VNTR) typing of Mycobacterium tuberculosis (Mtb) based on the multipurpose BioNumerics software. DNA from randomly selected isolates of Mtb from two European laboratories, including external control samples for MIRU-VNTR typing, were analysed. Samples were genotyped using the commercial 24-locus VNTR typing kit from GenoScreen. The PCR amplified fragments were separated by capillary electrophoresis. For the subsequent analyses, the currently used software GeneMapper was compared with BioNumerics. The endpoint was the level of concordance when comparing genotyping results obtained from BioNumerics with results obtained from GeneMapper and the ECDC proficiency study reference results. Also, the number of necessary manual standard size corrections and allele assignments in the two different software methods were compared. In total, 272 DNA samples, including the ECDC proficiency panel, were analysed. For all samples, there were 100% concordance of results. For a randomly selected set of 96 samples the numbers of manual corrections needed for size standards were 199 with GeneMapper versus zero for BioNumerics. The numbers of manual corrections for allele assignments were 122 with GeneMapper versus 16 with BioNumerics. In conclusion, we have validated the multipurpose software BioNumerics for standard 24-locus MIRU-VNTR typing and the software shows promising benefits in terms of simplification and minimization of hand-on time.

Partial Text

Tuberculosis (TB) remains a global public health hazard with estimated 10.4 million new cases and 1.4 million deaths in 2015 [1]. Despite overall declining incidences in Europe, the continent experiences 300,000–400,000 new TB cases yearly and faces challenges with multi-drug resistant strains of Mycobacterium tuberculosis (Mtb), which are prevalent in Eastern Europe and Asia in particular [2,3]. With political instability in European border regions and ongoing migration, control of Mtb transmission remains paramount. One key element to understand Mtb transmission dynamics and guide TB control is the genotyping of Mtb strains. Despite the development of higher resolution–but not yet standardized–methods based on whole genome sequencing, 24-locus mycobacterial interspersed repetitive unit-variable number-tandem repeat (MIRU-VNTR) typing remains widely used for genotyping because its standardization enables concerted national and international molecular surveillance of TB [3,4]. In multiple TB reference laboratories globally, MIRU-VNTR typing is performed using high throughput versions with multiplex PCR and fragment analysis on capillary sequencers [5,6]. Results from the fragment separation are analysed in the GeneMapper software, where electropherograms are visualized and processed for semi-automated allele calling [7]. However, analysing in GeneMapper is limited by the amount of manual corrections frequently needed for relabeling the size standard fragments and the subsequent allelic assignments of the MIRU-VNTR amplicons. In this study, we describe and validate a new, alternative procedure based on the multipurpose BioNumerics software [8,9] which addresses these limitations. This procedure allows integrating downstream operations completely and analysing the obtained genotypes using one single system, including databasing, attribution of genotype names synchronized with the MIRU-VNTRplus nomenclature [10], cluster analysis, and phylogenetic identification.

Randomly selected Mtb isolates from Institut Pasteur de Lille, France and International Reference Laboratory, Statens Serum Institut, Denmark, were used for analysis. Also, as an external control, DNA samples from European Center for Disease Control (ECDC) proficiency study for MIRU-VNTR typing were used for analysis. Samples were genotyped using the commercial 24-locus VNTR typing kit from GenoScreen [11] in accordance with the manufacturer’s instructions. The PCR amplified fragments were separated by capillary electrophoresis on ABI 3730 XL machines (Applied Biosystems) to determine the fragment sizes. The electrophoreses were calibrated beforehand using the calibration kit with the allelic ladder, also from GenoScreen [11]. GeneMapper version 5, Applied Biosystems, and BioNumerics version 7.6, Applied Maths, were used for the analysis in accordance with the user manuals [7,8]. The analyses of samples in GeneMapper and in BioNumerics were done independently and blindly in Copenhagen and Lille, respectively, i.e. during the analysis, there was no access to results or data from the other software. The primary endpoint was the level of concordance between results obtained from BioNumerics and results obtained from GeneMapper and the ECDC proficiency study results. The secondary endpoints were the number of manual standard size corrections and modifications of allele assignments needed in BioNumerics and GeneMapper, respectively.

Both the setup and the analysis using BioNumerics are described in detail in the supplemental material. In principle, BioNumerics works similarly to GeneMapper, that is i) electrophoresis data is imported as .fsa-files, ii) sizes of the size standard are specified automatically and any errors corrected manually, iii) alleles are assigned according to calculated sizes of the amplified fragments, and iv) 24-locus genotypes are obtained from aggregated alleles. The allele assignment is based on predefined sized bins, which are specified during initial setup of the database based on the experimental calibration of the sizes for different alleles of each of the 24 MIRU-VNTR loci upon electrophoresis, using the calibration kit with the allelic ladders. The attribution of existing and new genotype names is automatically done using the MIRU-VNTR plug-in, which synchronizes genotype names with the standard nomenclature and already registered genotypes maintained on the MIRU-VNTRplus website [12]. This is another significant difference compared to the use of GeneMapper, where the obtained genotypes have to be uploaded manually to the website for naming after genotypic analysis.

In this study performed in two European laboratories, we report the evaluation and validation of the use of BioNumerics for standard 24-locus MIRU-VNTR genotyping of Mtb. We found 100% concordance with the classical use of GeneMapper, and a substantial simplification and minimization of hands-on time in the overall workflow, due to a reduction of the amount of manual modifications of both size standards and allele assignments needed. We provide specific and detailed instructions on how to setup the software and how to perform the analysis using BioNumerics as supplemental material. Our study supplements the manufacturer’s manuals, enabling implementation of a simpler and faster workflow in many laboratories currently employing high throughput MIRU-VNTR typing using GeneMapper.

 

Source:

http://doi.org/10.1371/journal.pone.0205336

 

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