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Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications
BACKGROUND: Here we present a novel promising microbial diagnostic method that combines the sensitivity of Nucleic Acid Sequence Based Amplification (NASBA) with the high information content of microarray technology for the detection of bacterial tmRNA molecules. The NASBA protocol was modified to i...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685129/ https://www.ncbi.nlm.nih.gov/pubmed/19445684 http://dx.doi.org/10.1186/1472-6750-9-45 |
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author | Scheler, Ott Glynn, Barry Parkel, Sven Palta, Priit Toome, Kadri Kaplinski, Lauris Remm, Maido Maher, Majella Kurg, Ants |
author_facet | Scheler, Ott Glynn, Barry Parkel, Sven Palta, Priit Toome, Kadri Kaplinski, Lauris Remm, Maido Maher, Majella Kurg, Ants |
author_sort | Scheler, Ott |
collection | PubMed |
description | BACKGROUND: Here we present a novel promising microbial diagnostic method that combines the sensitivity of Nucleic Acid Sequence Based Amplification (NASBA) with the high information content of microarray technology for the detection of bacterial tmRNA molecules. The NASBA protocol was modified to include aminoallyl-UTP (aaUTP) molecules that were incorporated into nascent RNA during the NASBA reaction. Post-amplification labeling with fluorescent dye was carried out subsequently and tmRNA hybridization signal intensities were measured using microarray technology. Significant optimization of the labeled NASBA protocol was required to maintain the required sensitivity of the reactions. RESULTS: Two different aaUTP salts were evaluated and optimum final concentrations were identified for both. The final 2 mM concentration of aaUTP Li-salt in NASBA reaction resulted in highest microarray signals overall, being twice as high as the strongest signals with 1 mM aaUTP Na-salt. CONCLUSION: We have successfully demonstrated efficient combination of NASBA amplification technology with microarray based hybridization detection. The method is applicative for many different areas of microbial diagnostics including environmental monitoring, bio threat detection, industrial process monitoring and clinical microbiology. |
format | Text |
id | pubmed-2685129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26851292009-05-22 Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications Scheler, Ott Glynn, Barry Parkel, Sven Palta, Priit Toome, Kadri Kaplinski, Lauris Remm, Maido Maher, Majella Kurg, Ants BMC Biotechnol Methodology Article BACKGROUND: Here we present a novel promising microbial diagnostic method that combines the sensitivity of Nucleic Acid Sequence Based Amplification (NASBA) with the high information content of microarray technology for the detection of bacterial tmRNA molecules. The NASBA protocol was modified to include aminoallyl-UTP (aaUTP) molecules that were incorporated into nascent RNA during the NASBA reaction. Post-amplification labeling with fluorescent dye was carried out subsequently and tmRNA hybridization signal intensities were measured using microarray technology. Significant optimization of the labeled NASBA protocol was required to maintain the required sensitivity of the reactions. RESULTS: Two different aaUTP salts were evaluated and optimum final concentrations were identified for both. The final 2 mM concentration of aaUTP Li-salt in NASBA reaction resulted in highest microarray signals overall, being twice as high as the strongest signals with 1 mM aaUTP Na-salt. CONCLUSION: We have successfully demonstrated efficient combination of NASBA amplification technology with microarray based hybridization detection. The method is applicative for many different areas of microbial diagnostics including environmental monitoring, bio threat detection, industrial process monitoring and clinical microbiology. BioMed Central 2009-05-15 /pmc/articles/PMC2685129/ /pubmed/19445684 http://dx.doi.org/10.1186/1472-6750-9-45 Text en Copyright © 2009 Scheler 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 | Methodology Article Scheler, Ott Glynn, Barry Parkel, Sven Palta, Priit Toome, Kadri Kaplinski, Lauris Remm, Maido Maher, Majella Kurg, Ants Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications |
title | Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications |
title_full | Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications |
title_fullStr | Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications |
title_full_unstemmed | Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications |
title_short | Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications |
title_sort | fluorescent labeling of nasba amplified tmrna molecules for microarray applications |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685129/ https://www.ncbi.nlm.nih.gov/pubmed/19445684 http://dx.doi.org/10.1186/1472-6750-9-45 |
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