Abstract
The use of nucleic acid sequence-based amplification (NASBA), a continuous and isothermal method of in vitro nucleic acid amplification, was investigated for the specific identification of Escherichia coli (E. coli). A set of primers was selected from a highly conserved region of the 16S rRNA sequence of E. coli sandwiching a variable sequence to perform the amplification of bacterial RNA using NASBA. A probe was identified and shown to hybridize specifically to the amplified single-stranded RNA products of all tested E. coli isolates, including enterohemorrhagic serotype O157:H7. The high sensitivity of this assay system is most likely due to the large amplification power of NASBA and the high copy number of 16S rRNA. © Taylor & Francis Group, LLC.
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Kao, M. C., & Durst, R. A. (2010). Detection of Escherichia coli using nucleic acid sequence-based amplification and oligonucleotide probes for 16S ribosomal RNA. Analytical Letters, 43(10–11), 1756–1769. https://doi.org/10.1080/00032711003654005
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