MIRU-VNTR Genotyping of Mycobacterium tuberculosis Strains Using QIAxcel Technology: A Multicentre Evaluation Study.

Molecular genotyping of M.tuberculosis is an important laboratory tool in the context of emerging drug resistant TB. The standard 24-loci MIRU-VNTR typing includes PCR amplification followed by the detection and sizing of PCR fragments using capillary electrophoresis on automated sequencers or using...

Full description

Bibliographic Details
Main Authors: Vladyslav Nikolayevskyy, Alberto Trovato, Agnieszka Broda, Emanuele Borroni, Daniela Cirillo, Francis Drobniewski
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4777483?pdf=render
id doaj-24e32cccb547462ba8af5cd9464cd15f
record_format Article
spelling doaj-24e32cccb547462ba8af5cd9464cd15f2020-11-24T21:26:34ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01113e014943510.1371/journal.pone.0149435MIRU-VNTR Genotyping of Mycobacterium tuberculosis Strains Using QIAxcel Technology: A Multicentre Evaluation Study.Vladyslav NikolayevskyyAlberto TrovatoAgnieszka BrodaEmanuele BorroniDaniela CirilloFrancis DrobniewskiMolecular genotyping of M.tuberculosis is an important laboratory tool in the context of emerging drug resistant TB. The standard 24-loci MIRU-VNTR typing includes PCR amplification followed by the detection and sizing of PCR fragments using capillary electrophoresis on automated sequencers or using agarose gels. The QIAxcel Advanced system might offer a cost-effective medium-throughput alternative.Performance characteristics of the QIAxcel Advanced platform for the standard 24 VNTR loci panel was evaluated at two centres on a total of 140 DNA specimens using automated capillary electrophoresis as a reference method. Additionally 4 hypervariable MIRU-VNTR loci were evaluated on 53 crude DNA extracts. The sizing accuracy, interlaboratory reproducibility and overall instrument's performance were assessed during the study.An overall concordance with the reference method was high reaching 98.5% and 97.6% for diluted genomic and crude DNA extracts respectively. 91.4% of all discrepancies were observed in fragments longer than 700bp. The concordance for hypervariable loci was lower except for locus 4120 (96.2%). The interlaboratory reproducibility agreement rates were 98.9% and 91.3% for standard and hypervariable loci, respectively. Overall performance of the QIAxcel platform for M.tuberculosis genotyping using a panel of standard loci is comparable to that of established methods for PCR fragments up to 700bp. Inaccuracies in sizing of longer fragments could be resolved through using in-house size markers or introduction of offset values. To conclude, the QiaXcel system could be considered an effective alternative to existing methods in smaller reference and regional laboratories offering good performance and shorter turnaround times.http://europepmc.org/articles/PMC4777483?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Vladyslav Nikolayevskyy
Alberto Trovato
Agnieszka Broda
Emanuele Borroni
Daniela Cirillo
Francis Drobniewski
spellingShingle Vladyslav Nikolayevskyy
Alberto Trovato
Agnieszka Broda
Emanuele Borroni
Daniela Cirillo
Francis Drobniewski
MIRU-VNTR Genotyping of Mycobacterium tuberculosis Strains Using QIAxcel Technology: A Multicentre Evaluation Study.
PLoS ONE
author_facet Vladyslav Nikolayevskyy
Alberto Trovato
Agnieszka Broda
Emanuele Borroni
Daniela Cirillo
Francis Drobniewski
author_sort Vladyslav Nikolayevskyy
title MIRU-VNTR Genotyping of Mycobacterium tuberculosis Strains Using QIAxcel Technology: A Multicentre Evaluation Study.
title_short MIRU-VNTR Genotyping of Mycobacterium tuberculosis Strains Using QIAxcel Technology: A Multicentre Evaluation Study.
title_full MIRU-VNTR Genotyping of Mycobacterium tuberculosis Strains Using QIAxcel Technology: A Multicentre Evaluation Study.
title_fullStr MIRU-VNTR Genotyping of Mycobacterium tuberculosis Strains Using QIAxcel Technology: A Multicentre Evaluation Study.
title_full_unstemmed MIRU-VNTR Genotyping of Mycobacterium tuberculosis Strains Using QIAxcel Technology: A Multicentre Evaluation Study.
title_sort miru-vntr genotyping of mycobacterium tuberculosis strains using qiaxcel technology: a multicentre evaluation study.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description Molecular genotyping of M.tuberculosis is an important laboratory tool in the context of emerging drug resistant TB. The standard 24-loci MIRU-VNTR typing includes PCR amplification followed by the detection and sizing of PCR fragments using capillary electrophoresis on automated sequencers or using agarose gels. The QIAxcel Advanced system might offer a cost-effective medium-throughput alternative.Performance characteristics of the QIAxcel Advanced platform for the standard 24 VNTR loci panel was evaluated at two centres on a total of 140 DNA specimens using automated capillary electrophoresis as a reference method. Additionally 4 hypervariable MIRU-VNTR loci were evaluated on 53 crude DNA extracts. The sizing accuracy, interlaboratory reproducibility and overall instrument's performance were assessed during the study.An overall concordance with the reference method was high reaching 98.5% and 97.6% for diluted genomic and crude DNA extracts respectively. 91.4% of all discrepancies were observed in fragments longer than 700bp. The concordance for hypervariable loci was lower except for locus 4120 (96.2%). The interlaboratory reproducibility agreement rates were 98.9% and 91.3% for standard and hypervariable loci, respectively. Overall performance of the QIAxcel platform for M.tuberculosis genotyping using a panel of standard loci is comparable to that of established methods for PCR fragments up to 700bp. Inaccuracies in sizing of longer fragments could be resolved through using in-house size markers or introduction of offset values. To conclude, the QiaXcel system could be considered an effective alternative to existing methods in smaller reference and regional laboratories offering good performance and shorter turnaround times.
url http://europepmc.org/articles/PMC4777483?pdf=render
work_keys_str_mv AT vladyslavnikolayevskyy miruvntrgenotypingofmycobacteriumtuberculosisstrainsusingqiaxceltechnologyamulticentreevaluationstudy
AT albertotrovato miruvntrgenotypingofmycobacteriumtuberculosisstrainsusingqiaxceltechnologyamulticentreevaluationstudy
AT agnieszkabroda miruvntrgenotypingofmycobacteriumtuberculosisstrainsusingqiaxceltechnologyamulticentreevaluationstudy
AT emanueleborroni miruvntrgenotypingofmycobacteriumtuberculosisstrainsusingqiaxceltechnologyamulticentreevaluationstudy
AT danielacirillo miruvntrgenotypingofmycobacteriumtuberculosisstrainsusingqiaxceltechnologyamulticentreevaluationstudy
AT francisdrobniewski miruvntrgenotypingofmycobacteriumtuberculosisstrainsusingqiaxceltechnologyamulticentreevaluationstudy
_version_ 1725978912357351424