Abstract
A real-time nucleic acid sequence-based amplification assay, targeting tmRNA, was designed for the rapid identification of Staphylococcus aureus. The selectivity of the assay was confirmed against a panel of 76 Staphylococcus strains and species and 22 other bacterial species. A detection limit of 1 cell equivalent was determined for the assay. A chimeric in vitro transcribed internal amplification control was developed and included in the assay. Application of the assay in natural and artificially contaminated unpasteurized (raw) milk enabled detection of 1-10 CFUS. aureus mL-1 in 3-4 h, without the need for culture enrichment. Staphylococcus aureus was detected in all artificially contaminated milk samples (n=20) and none of the natural milk samples (n=20). Microbiological analysis of the natural milk samples was performed in parallel according to ISO 6888-3 and confirmed the absence of S. aureus. The method developed in this study has the potential to enable the specific detection of S. aureus in raw milk in a significantly shorter time frame than current standard methods. The assay further demonstrates the usefulness of tmRNA ssrA as a nucleic acid diagnostic target.
Original language | English (Ireland) |
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Pages (from-to) | 218-223 |
Number of pages | 6 |
Journal | Fems Microbiology Letters |
Volume | 301 |
Issue number | 2 |
DOIs | |
Publication status | Published - 1 Dec 2009 |
Keywords
- Internal amplification control (IAC)
- Milk
- Real-time NASBA
- Staphylococcus aureus
- TmRNA
Authors (Note for portal: view the doc link for the full list of authors)
- Authors
- O'Grady, J,Lacey, K,Glynn, B,Smith, TJ,Barry, T,Maher, M