Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout

RNA. 2020 Sep;26(9):1283-1290. doi: 10.1261/rna.075192.120. Epub 2020 Jun 1.

Abstract

Isothermal, cell-free, synthetic biology-based approaches to pathogen detection leverage the power of tools available in biological systems, such as highly active polymerases compatible with lyophilization, without the complexity inherent to live-cell systems, of which nucleic acid sequence based amplification (NASBA) is well known. Despite the reduced complexity associated with cell-free systems, side reactions are a common characteristic of these systems. As a result, these systems often exhibit false positives from reactions lacking an amplicon. Here we show that the inclusion of a DNA duplex lacking a promoter and unassociated with the amplicon fully suppresses false positives, enabling a suite of fluorescent aptamers to be used as NASBA tags (Apta-NASBA). Apta-NASBA has a 1 pM detection limit and can provide multiplexed, multicolor fluorescent readout. Furthermore, Apta-NASBA can be performed using a variety of equipment, for example, a fluorescence microplate reader, a qPCR instrument, or an ultra-low-cost Raspberry Pi-based 3D-printed detection platform using a cell phone camera module, compatible with field detection.

Keywords: NASBA; T7 RNA polymerase; fluorescent aptamer; isothermal amplification; pathogen detection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aptamers, Nucleotide / chemistry*
  • Cell-Free System
  • Fluorescence
  • Fluorescent Dyes / chemistry*
  • Humans
  • Oligonucleotides / chemistry*
  • Polymerase Chain Reaction / methods*
  • Promoter Regions, Genetic / genetics
  • Self-Sustained Sequence Replication / methods*
  • Sensitivity and Specificity

Substances

  • Aptamers, Nucleotide
  • Fluorescent Dyes
  • Oligonucleotides