Integrated microfluidic tmRNA purification and real-time NASBA device for molecular diagnostics

Lab Chip. 2008 Dec;8(12):2071-8. doi: 10.1039/b812515e. Epub 2008 Oct 24.

Abstract

We demonstrate the first integrated microfluidic tmRNA purification and nucleic acid sequence-based amplification (NASBA) device incorporating real-time detection. The real-time amplification and detection step produces pathogen-specific response in < 3 min from the chip-purified RNA from 100 lysed bacteria. On-chip RNA purification uses a new silica bead immobilization method. On-chip amplification uses custom-designed high-selectivity primers and real-time detection uses molecular beacon fluorescent probe technology; both are integrated on-chip with NASBA. Present in all bacteria, tmRNA (10Sa RNA) includes organism-specific identification sequences, exhibits unusually high stability relative to mRNA, and has high copy number per organism; the latter two factors improve the limit of detection, accelerate time-to-positive response, and suit this approach ideally to the detection of small numbers of bacteria. Device efficacy was demonstrated by integrated on-chip purification, amplification, and real-time detection of 100 E. coli bacteria in 100 microL of crude lysate in under 30 min for the entire process.

MeSH terms

  • Diagnostic Techniques and Procedures*
  • Escherichia coli / chemistry
  • Microfluidics* / instrumentation
  • Microfluidics* / methods
  • RNA, Bacterial / chemistry*
  • Self-Sustained Sequence Replication* / instrumentation
  • Self-Sustained Sequence Replication* / methods

Substances

  • RNA, Bacterial
  • tmRNA