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Comparison of commercial DNA preparation kits for the detection of Brucellae in tissue using quantitative real-time PCR

BACKGROUND: The detection of Brucellae in tissue specimens using PCR assays is difficult because the amount of bacteria is usually low. Therefore, optimised DNA extraction methods are critical. The aim of this study was to assess the performance of commercial kits for the extraction of Brucella DNA....

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Autores principales: Tomaso, Herbert, Kattar, Mireille, Eickhoff, Meike, Wernery, Ulrich, Al Dahouk, Sascha, Straube, Eberhard, Neubauer, Heinrich, Scholz, Holger C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873554/
https://www.ncbi.nlm.nih.gov/pubmed/20403208
http://dx.doi.org/10.1186/1471-2334-10-100
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author Tomaso, Herbert
Kattar, Mireille
Eickhoff, Meike
Wernery, Ulrich
Al Dahouk, Sascha
Straube, Eberhard
Neubauer, Heinrich
Scholz, Holger C
author_facet Tomaso, Herbert
Kattar, Mireille
Eickhoff, Meike
Wernery, Ulrich
Al Dahouk, Sascha
Straube, Eberhard
Neubauer, Heinrich
Scholz, Holger C
author_sort Tomaso, Herbert
collection PubMed
description BACKGROUND: The detection of Brucellae in tissue specimens using PCR assays is difficult because the amount of bacteria is usually low. Therefore, optimised DNA extraction methods are critical. The aim of this study was to assess the performance of commercial kits for the extraction of Brucella DNA. METHODS: Five kits were evaluated using clinical specimens: QIAamp™ DNA Mini Kit (QIAGEN), peqGold™ Tissue DNA Mini Kit (PeqLab), UltraClean™ Tissue and Cells DNA Isolation Kit (MoBio), DNA Isolation Kit for Cells and Tissues (Roche), and NucleoSpin™ Tissue (Macherey-Nagel). DNA yield was determined using a quantitative real-time PCR assay targeting IS711 that included an internal amplification control. RESULTS: Kits of QIAGEN and Roche provided the highest amount of DNA, Macherey-Nagel and Peqlab products were intermediate whereas MoBio yielded the lowest amount of DNA. Differences were significant (p < 0.05) and of diagnostic relevance. Sample volume, elution volume, and processing time were also compared. CONCLUSIONS: We observed differences in DNA yield as high as two orders of magnitude for some samples between the best and the worst DNA extraction kits and inhibition was observed occasionally. This indicates that DNA purification may be more relevant than expected when the amount of DNA in tissue is very low.
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spelling pubmed-28735542010-05-20 Comparison of commercial DNA preparation kits for the detection of Brucellae in tissue using quantitative real-time PCR Tomaso, Herbert Kattar, Mireille Eickhoff, Meike Wernery, Ulrich Al Dahouk, Sascha Straube, Eberhard Neubauer, Heinrich Scholz, Holger C BMC Infect Dis Research Article BACKGROUND: The detection of Brucellae in tissue specimens using PCR assays is difficult because the amount of bacteria is usually low. Therefore, optimised DNA extraction methods are critical. The aim of this study was to assess the performance of commercial kits for the extraction of Brucella DNA. METHODS: Five kits were evaluated using clinical specimens: QIAamp™ DNA Mini Kit (QIAGEN), peqGold™ Tissue DNA Mini Kit (PeqLab), UltraClean™ Tissue and Cells DNA Isolation Kit (MoBio), DNA Isolation Kit for Cells and Tissues (Roche), and NucleoSpin™ Tissue (Macherey-Nagel). DNA yield was determined using a quantitative real-time PCR assay targeting IS711 that included an internal amplification control. RESULTS: Kits of QIAGEN and Roche provided the highest amount of DNA, Macherey-Nagel and Peqlab products were intermediate whereas MoBio yielded the lowest amount of DNA. Differences were significant (p < 0.05) and of diagnostic relevance. Sample volume, elution volume, and processing time were also compared. CONCLUSIONS: We observed differences in DNA yield as high as two orders of magnitude for some samples between the best and the worst DNA extraction kits and inhibition was observed occasionally. This indicates that DNA purification may be more relevant than expected when the amount of DNA in tissue is very low. BioMed Central 2010-04-20 /pmc/articles/PMC2873554/ /pubmed/20403208 http://dx.doi.org/10.1186/1471-2334-10-100 Text en Copyright ©2010 Tomaso et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tomaso, Herbert
Kattar, Mireille
Eickhoff, Meike
Wernery, Ulrich
Al Dahouk, Sascha
Straube, Eberhard
Neubauer, Heinrich
Scholz, Holger C
Comparison of commercial DNA preparation kits for the detection of Brucellae in tissue using quantitative real-time PCR
title Comparison of commercial DNA preparation kits for the detection of Brucellae in tissue using quantitative real-time PCR
title_full Comparison of commercial DNA preparation kits for the detection of Brucellae in tissue using quantitative real-time PCR
title_fullStr Comparison of commercial DNA preparation kits for the detection of Brucellae in tissue using quantitative real-time PCR
title_full_unstemmed Comparison of commercial DNA preparation kits for the detection of Brucellae in tissue using quantitative real-time PCR
title_short Comparison of commercial DNA preparation kits for the detection of Brucellae in tissue using quantitative real-time PCR
title_sort comparison of commercial dna preparation kits for the detection of brucellae in tissue using quantitative real-time pcr
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873554/
https://www.ncbi.nlm.nih.gov/pubmed/20403208
http://dx.doi.org/10.1186/1471-2334-10-100
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