Literature DB >> 35027876

Saliva "Treat-and-Heat" Triplex Reverse Transcription Loop-Mediated Isothermal Amplification Assay for SARS-CoV-2.

Marie J Y Reolo1, Carlos S R Eleazar1, Joseph P Sonio1, Ryonne T Solon1, Janika L B Villamor1, Alexandra K Loedin1, Keith J M Moore1.   

Abstract

The demand for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) molecular diagnostics that are faster, cheaper, and simpler to run than nasopharyngeal-based reverse transcription quantitative PCR (RT-qPCR) tests remains unmet in many parts of the world. In the Philippines, geographical and economic access to quality diagnostic testing remains out of reach for many communities. We describe the preclinical development of a fluorescence-based reverse transcription loop-mediated isothermal amplification test that uses drooled saliva as the biospecimen. Six treat-and-heat ("direct") procedures that inactivate the virus and release the target RNA were compared. Using duplexed As1e and E1 primers, protocols derived from Ben-Assa et al. (2020) using proteinase K or from Rabe and Cepko (2020) using TCEP (Tris(2-carboxyethyl)phosphine hydrochloride)/EDTA provided reliable RNA amplification. The TCEP/EDTA-based method in particular showed improvement in robustness in duplex vs. singleplex format. Inclusion of human β-actin primers provided a triplex test with an internal amplification control that could be distinguished from SARS-CoV-2 amplicons based on melt curve analysis. After including the dUTP/uracil-DNA glycosylase system and implementing laboratory procedures to avoid cross-contamination, false positive amplification was acceptably rare. The duplex or triplex tests are predicted to reliably detect patient salivary viral loads >100 copies/μL and to yield equivocal results between 10 and 100 copies/μL. These viral loads, corresponding to RT-qPCR C t ∼29-32, are expected to identify the majority of infected and, particularly, of infectious patients. If clinically validated, the test would provide additional testing capacity requiring only a fraction of the time, cost, and infrastructure of the current nasopharyngeal swab-based RT-qPCR test, thereby improving access to testing for more Filipinos.
© 2021 ABRF.

Entities:  

Keywords:  Proteinase K; extraction-free; fluorescence; melt curve

Mesh:

Substances:

Year:  2021        PMID: 35027876      PMCID: PMC8730512          DOI: 10.7171/jbt.21-3203-014

Source DB:  PubMed          Journal:  J Biomol Tech        ISSN: 1524-0215


  34 in total

1.  Enhancing colorimetric loop-mediated isothermal amplification speed and sensitivity with guanidine chloride.

Authors:  Yinhua Zhang; Guoping Ren; Jackson Buss; Andrew J Barry; Gregory C Patton; Nathan A Tanner
Journal:  Biotechniques       Date:  2020-07-08       Impact factor: 1.993

2.  Simultaneous elimination of carryover contamination and detection of DNA with uracil-DNA-glycosylase-supplemented loop-mediated isothermal amplification (UDG-LAMP).

Authors:  Kuangwen Hsieh; Peter L Mage; Andrew T Csordas; Michael Eisenstein; H Tom Soh
Journal:  Chem Commun (Camb)       Date:  2014-02-28       Impact factor: 6.222

3.  Rapid and Extraction-Free Detection of SARS-CoV-2 from Saliva by Colorimetric Reverse-Transcription Loop-Mediated Isothermal Amplification.

Authors:  Matthew A Lalli; Joshua S Langmade; Xuhua Chen; Catrina C Fronick; Christopher S Sawyer; Lauren C Burcea; Michael N Wilkinson; Robert S Fulton; Michael Heinz; William J Buchser; Richard D Head; Robi D Mitra; Jeffrey Milbrandt
Journal:  Clin Chem       Date:  2021-01-30       Impact factor: 8.327

4.  Rethinking Covid-19 Test Sensitivity - A Strategy for Containment.

Authors:  Michael J Mina; Roy Parker; Daniel B Larremore
Journal:  N Engl J Med       Date:  2020-09-30       Impact factor: 91.245

Review 5.  Upper respiratory tract sampling in COVID-19.

Authors:  A Mawaddah; H S Gendeh; S G Lum; M B Marina
Journal:  Malays J Pathol       Date:  2020-04       Impact factor: 0.656

6.  One-Pot Reverse Transcriptional Loop-Mediated Isothermal Amplification (RT-LAMP) for Detecting MERS-CoV.

Authors:  Se Hee Lee; Yun Hee Baek; Yang-Hoon Kim; Young-Ki Choi; Min-Suk Song; Ji-Young Ahn
Journal:  Front Microbiol       Date:  2017-01-09       Impact factor: 5.640

7.  High-Surety Isothermal Amplification and Detection of SARS-CoV-2.

Authors:  Sanchita Bhadra; Timothy E Riedel; Simren Lakhotia; Nicholas D Tran; Andrew D Ellington
Journal:  mSphere       Date:  2021-05-19       Impact factor: 4.389

8.  Viral RNA load as determined by cell culture as a management tool for discharge of SARS-CoV-2 patients from infectious disease wards.

Authors:  Bernard La Scola; Marion Le Bideau; Julien Andreani; Van Thuan Hoang; Clio Grimaldier; Philippe Colson; Philippe Gautret; Didier Raoult
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2020-04-27       Impact factor: 3.267

9.  Saliva as a gold-standard sample for SARS-CoV-2 detection.

Authors:  Steph H Tan; Orchid Allicock; Mari Armstrong-Hough; Anne L Wyllie
Journal:  Lancet Respir Med       Date:  2021-04-19       Impact factor: 30.700

10.  An enhanced isothermal amplification assay for viral detection.

Authors:  Jason Qian; Sarah A Boswell; Christopher Chidley; Zhi-Xiang Lu; Mary E Pettit; Benjamin L Gaudio; Jesse M Fajnzylber; Ryan T Ingram; Rebecca H Ward; Jonathan Z Li; Michael Springer
Journal:  Nat Commun       Date:  2020-11-20       Impact factor: 14.919

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