Evidence map›Paper›PMID 34106115›Full record

ArticleThe Analyst2021

Padlock probe-based rolling circle amplification lateral flow assay for point-of-need nucleic acid detection.

Sidhartha Jain, David S Dandy, Brian J Geiss, Charles S Henry

Open access · greenAbstract read
In one paragraph

Article in The Analyst, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Sidhartha JainSchool of Biomedical Engineering, Colorado State University, Fort Collins, CO 80523, USA. chuck.henry@colostate.edu.
David S DandySchool of Biomedical Engineering, Colorado State University, Fort Collins, CO 80523, USA. chuck.henry@colostate.edu and Department of Chemical and Biological Engineering, Colorado State University, Fort Collins, CO 80523, USA.ORCID http://orcid.org/0000-0003-3254-0717
Brian J GeissSchool of Biomedical Engineering, Colorado State University, Fort Collins, CO 80523, USA. chuck.henry@colostate.edu and Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, CO 80523, USA.ORCID http://orcid.org/0000-0001-8180-5772
Charles S HenrySchool of Biomedical Engineering, Colorado State University, Fort Collins, CO 80523, USA. chuck.henry@colostate.edu and Department of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.ORCID http://orcid.org/0000-0002-8671-7728
Colorado State University · US

Funding

Low-Cost Versatile Sampler for Personal PM Exposure by MicroenvironmentR33ES024719 · NIEHS · COLORADO STATE UNIVERSITY · PI HENRY, CHARLES S, VOLCKENS, JOHN · 2017 to 2020
$2.1M
Mechanism of Flavivirus RNA CappingR01AI132668 · NIAID · COLORADO STATE UNIVERSITY · PI GEISS, BRIAN · 2018 to 2022
$1.9M
NIAID NIH HHS R01 AI132668NIEHS NIH HHS R33 ES024719
6 · The paper itself

Abstract

Sensitive, reliable and cost-effective detection of pathogens has wide ranging applications in clinical diagnostics and therapeutics, water and food safety, environmental monitoring, biosafety and epidemiology. Nucleic acid amplification tests (NAATs) such as PCR and isothermal amplification methods provide excellent analytical performance and significantly faster turnaround times than conventional culture-based methods. However, the inherent cost and complexity of NAATs limit their application in resource-limited settings and the developing world. To help address this urgent need, we have developed a sensitive method for nucleic acid analysis based on padlock probe rolling circle amplification (PLRCA), nuclease protection (NP) and lateral flow detection (LFA), referred to as PLAN-LFA, that can be used in resource-limited settings. The assay involves solution-phase hybridization of a padlock probe to target, sequence-specific ligation of the probe to form a circular template that undergoes isothermal rolling circle amplification in the presence of a polymerase and a labeled probe DNA. The RCA product is a long, linear concatenated single-stranded DNA that contains binding sites for the labeled probe. The sample is then exposed to a nuclease which selectively cleaves single-stranded DNA, the double-stranded labeled probe is protected from nuclease digestion and detected in a lateral flow immunoassay format to provide a visual, colorimetric readout of results. We have developed specific assays targeting beta-lactamase resistance gene for monitoring of antimicrobial resistance and Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2, the novel coronavirus discovered in 2019) using the PLAN-LFA platform. The assay provides a limit of detection of 1.1 pM target DNA (or 1.3 × 106 copies per reaction). We also demonstrate the versatility and robustness of the method by performing analysis on DNA and RNA targets, and perform analysis in complex sample matrices like saliva, plant tissue extract and bacterial culture without any sample pretreatment steps.

Indexed as

COVID-19SARS-CoV-2DNA ProbesHumansNucleic Acid Amplification TechniquesNucleic Acid HybridizationDNA Probes

Identifiers

PMID34106115
PMCPMC8294176
OpenAlexW3165973276

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.