Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout

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 employing a cell phone camera module, compatible with field detection.

[1]  K. Arikawa,et al.  Multiplex real‐time PCR for exhaustive detection of diarrhoeagenic Escherichia coli , 2009, Journal of applied microbiology.

[2]  D. Tweardy,et al.  INFECTION AND IMMUNITY , 2006, Infection and Immunity.

[3]  J. Piccirilli,et al.  A G-Quadruplex-Containing RNA Activates Fluorescence in a GFP-Like Fluorophore , 2014, Nature chemical biology.

[4]  C. Wilson,et al.  Laser-mediated, site-specific inactivation of RNA transcripts. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[5]  Lauren M. Aufdembrink,et al.  DNA transistors switched by the Hofmeister effect , 2019 .

[6]  D. Wiedbrauk Molecular Methods for Virus Detection , 1992 .

[7]  A. Ferré-D’Amaré,et al.  Structural basis for activity of highly efficient RNA mimics of green fluorescent protein , 2014, Nature Structural &Molecular Biology.

[8]  J. Nataro,et al.  Characterization of the AggR Regulon in Enteroaggregative Escherichia coli , 2012, Infection and Immunity.

[9]  J. Compton,et al.  Nucleic acid sequence-based amplification , 1991, Nature.

[10]  Henry A. Erlich,et al.  The polymerase chain reaction. , 1989, Trends in genetics : TIG.

[11]  Lyndon Gommersall,et al.  Basic principles of real-time quantitative PCR , 2005, Expert review of molecular diagnostics.

[12]  R. Tsien,et al.  Aptamers switch on fluorescence of triphenylmethane dyes. , 2003, Journal of the American Chemical Society.

[13]  Shihab U. Sobuz,et al.  A Laboratory-Developed TaqMan Array Card for Simultaneous Detection of 19 Enteropathogens , 2012, Journal of Clinical Microbiology.

[14]  Olaf Piepenburg,et al.  DNA Detection Using Recombination Proteins , 2006, PLoS biology.

[15]  Xing Li,et al.  Imaging RNA polymerase III transcription using a photostable RNA-fluorophore complex , 2017, Nature chemical biology.

[16]  T. Notomi,et al.  Loop-mediated isothermal amplification of DNA. , 2000, Nucleic acids research.

[17]  Sadeem Ahmad,et al.  An origin of the immunogenicity of in vitro transcribed RNA , 2018, bioRxiv.

[18]  M. Plikus,et al.  Organotypic skin culture. , 2013, The Journal of investigative dermatology.

[19]  G. Tzertzinis,et al.  Synthesis of low immunogenicity RNA with high-temperature in vitro transcription. , 2020, RNA.

[20]  S. Sastry,et al.  Nuclease Activity of T7 RNA Polymerase and the Heterogeneity of Transcription Elongation Complexes* , 1997, The Journal of Biological Chemistry.

[21]  P. Puntervoll,et al.  Towards Rational Design of a Toxoid Vaccine against the Heat-Stable Toxin of Escherichia coli , 2016, Infection and Immunity.

[22]  R. Sooknanan,et al.  12 – Nucleic Acid Sequence-Based Amplification , 1995 .

[23]  I. Ichetovkin,et al.  Substrate Recognition by the Leucyl/Phenylalanyl-tRNA-protein Transferase , 1997, The Journal of Biological Chemistry.

[24]  B. Deiman,et al.  Characteristics and applications of nucleic acid sequence-based amplification (NASBA) , 2002, Molecular biotechnology.

[25]  Hyun-Jin Kim,et al.  Characterization of a Thermostable UvrD Helicase and Its Participation in Helicase-dependent Amplification* , 2005, Journal of Biological Chemistry.

[26]  Aviv Regev,et al.  Nucleic acid detection with CRISPR-Cas13a/C2c2 , 2017, Science.

[27]  Robert Batey,et al.  Faculty Opinions recommendation of Broccoli: rapid selection of an RNA mimic of green fluorescent protein by fluorescence-based selection and directed evolution. , 2014 .

[28]  J Ring,et al.  Characterization of T7-specific ribonucleic acid polymerase. II. Inhibitors of the enzyme and their application to the study of the enzymatic reaction. , 1973, The Journal of biological chemistry.

[29]  Samie R. Jaffrey,et al.  RNA mimics of green fluorescent protein , 2013 .

[30]  E. Dolgosheina,et al.  RNA detection with high specificity and sensitivity using nested fluorogenic Mango NASBA , 2019, RNA.

[31]  K. Inouye,et al.  Increase in thermal stability of Moloney murine leukaemia virus reverse transcriptase by site-directed mutagenesis. , 2010, Journal of biotechnology.

[32]  Grigory S. Filonov,et al.  Broccoli: Rapid Selection of an RNA Mimic of Green Fluorescent Protein by Fluorescence-Based Selection and Directed Evolution , 2014, Journal of the American Chemical Society.

[33]  Samie R. Jaffrey,et al.  A homodimer interface without base pairs in an RNA mimic of red fluorescent protein , 2017, Nature chemical biology.

[34]  P. Plourde Travellers' diarrhea in children. , 2003, Paediatrics & child health.

[35]  G. Tzertzinis,et al.  Synthesis of low immunogenicity RNA with high-temperature in vitro transcription , 2019, bioRxiv.

[36]  J. Ofengand,et al.  Use of inorganic pyrophosphatase to improve the yield of in vitro transcription reactions catalyzed by T7 RNA polymerase. , 1990, BioTechniques.

[37]  Erin E. Carlson,et al.  Real-Time Visualization of in Vitro Transcription of a Fluorescent RNA Aptamer: An Experiment for the Upper-Division Undergraduate or First-Year Graduate Laboratory , 2018, Journal of Chemical Education.

[38]  R. Linhardt,et al.  Heparin-protein interactions. , 2002, Angewandte Chemie.