BMC Biotechnology (May 2009)

Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications

  • Kaplinski Lauris,
  • Toome Kadri,
  • Palta Priit,
  • Parkel Sven,
  • Glynn Barry,
  • Scheler Ott,
  • Remm Maido,
  • Maher Majella,
  • Kurg Ants

DOI
https://doi.org/10.1186/1472-6750-9-45
Journal volume & issue
Vol. 9, no. 1
p. 45

Abstract

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Abstract 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.