Evidence map›Paper›PMID 32948855›Full record

ArticleNature biomedical engineering2020

Sensitive fluorescence detection of SARS-CoV-2 RNA in clinical samples via one-pot isothermal ligation and transcription.

Chang Ha Woo, Sungho Jang, Giyoung Shin, Gyoo Yeol Jung, Jeong Wook Lee

Open access · bronzeAbstract read
In one paragraph

Article in Nature biomedical engineering, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
10.9field-weighted citation impact, top 1% 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

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 192 citations in OpenAlex.

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13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Chang Ha Woo *School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, Pohang, Republic of Korea.ORCID http://orcid.org/0000-0003-1568-4700
Sungho Jang *Department of Chemical Engineering, Pohang University of Science and Technology, Pohang, Republic of Korea.ORCID http://orcid.org/0000-0003-4368-3043
Giyoung ShinSchool of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, Pohang, Republic of Korea.
Gyoo Yeol JungSchool of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, Pohang, Republic of Korea. gyjung@postech.ac.kr.ORCID http://orcid.org/0000-0002-9742-3207
Jeong Wook LeeSchool of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, Pohang, Republic of Korea. jeongwook@postech.ac.kr.ORCID http://orcid.org/0000-0003-0705-0177
Pohang University of Science and Technology · KR

Funding

Ministry of Knowledge Economy | Korea Institute of Energy Technology Evaluation and Planning (KETEP) No. 20194030202330National Research Foundation of Korea (NRF) No. 2018R1C1B3007409National Research Foundation of Korea (NRF) No. 2019R1A2C2008680National Research Foundation of Korea (NRF) NRF-2018M3D3A1A01055754
6 · The paper itself

Abstract

The control of viral outbreaks requires nucleic acid diagnostic tests that are sensitive, simple and fast. Here, we report a highly sensitive and specific one-pot assay for the fluorescence-based detection of RNA from pathogens. The assay, which can be performed within 30-50 min of incubation time and can reach a limit of detection of 0.1-attomolar RNA concentration, relies on a sustained isothermal reaction cascade producing an RNA aptamer that binds to a fluorogenic dye. The RNA aptamer is transcribed by the T7 RNA polymerase from the ligation product of a promoter DNA probe and a reporter DNA probe that hybridize with the target single-stranded RNA sequence via the SplintR ligase (a Chlorella virus DNA ligase). In 40 nasopharyngeal SARS-CoV-2 samples, the assay reached positive and negative predictive values of 95 and 100%, respectively. We also show that the assay can rapidly detect a range of viral and bacterial RNAs.

Indexed as

ChlorellaCOVID-19Diagnostic Tests, RoutineDNADNA-Directed RNA PolymerasesDNA LigasesFluorescenceHumansMolecular Diagnostic TechniquesNucleic Acid Amplification TechniquesPandemicsRNA, ViralSARS-CoV-2Sensitivity and SpecificityTranscription, GeneticViral Proteinsbacteriophage T7 RNA polymeraseChlorella virus DNA ligaseDNADNA-Directed RNA PolymerasesDNA LigasesRNA, ViralViral Proteins

Identifiers

PMID32948855
PMCPMC7499000
OpenAlexW3087583316

What OpenQuestion holds

Textmetadata
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.