Evidence map›Paper›PMID 35294970›Full record

ArticleBioinformatics (Oxford, England)2022

Evitar: designing anti-viral RNA therapies against future RNA viruses.

Dingyao Zhang, Jingru Tian, Yadong Wang, Jun Lu

Open access · greenAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 60% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

  • Update of
    2020
5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Dingyao ZhangYale Stem Cell Center, Yale University, New Haven, CT 06520, USA.
Jingru TianYale Stem Cell Center, Yale University, New Haven, CT 06520, USA.
Yadong WangYale Stem Cell Center, Yale University, New Haven, CT 06520, USA.
Jun LuYale Stem Cell Center, Yale University, New Haven, CT 06520, USA.ORCID 0000-0003-2726-7613
Yale Cancer Center · US

Funding

Yale Cooperative Hematology Specialized Core CenterU54DK106857 · NIDDK · YALE UNIVERSITY · PI JOHN HWA, Diane S Krause · 2015 to 2026
$9.7M
Quantitative Modeling of MicroRNA:Target Interactions in Cell Fate TransitionR01GM116855 · NIGMS · WADSWORTH CENTER · PI DING, YE, LU, JUN · 2016 to 2019
$2.2M
Novel Bioinformatics Tools for Quantitative Prediction of Primary MicroRNA ProcessingR01GM138856 · NIGMS · YALE UNIVERSITY · PI DING, YE, LU, JUN · 2020 to 2023
$1.8M
High-throughput single-cell co-sequencing of small and large RNAs to identify molecular circuitry in cancerR33CA246711 · NCI · YALE UNIVERSITY · PI FAN, RONG, LU, JUN · 2020 to 2022
$1.2M
CRISPR-based Enhanced Molecular Chipper Technology for Identifying Functional Noncoding Elements in CancerR33CA225863 · NCI · YALE UNIVERSITY · PI LU, JUN · 2018 to 2020
$1.2M
NCI NIH HHS R33 CA225863NCI NIH HHS R33 CA246711NIDDK NIH HHS U54 DK106857NIGMS NIH HHS R01 GM116855NIGMS NIH HHS R01 GM138856
6 · The paper itself

Abstract

motivationThe coronavirus disease 2019 (COVID-19) pandemic has highlighted the threat of emerging respiratory viruses and has exposed the lack of availability of off-the-shelf therapeutics against new RNA viruses. Previous research has established the potential that siRNAs and RNA-targeting CRISPR have in combating known RNA viruses. However, the feasibility and tools for designing anti-viral RNA therapeutics against future RNA viruses have not yet been established.

resultsWe develop the Emerging-Virus-Targeting RNA (Evitar) pipeline for designing anti-viral siRNAs and CRISPR Cas13a guide RNA (gRNA) sequences. Within Evitar, we develop Greedy Algorithm with Redundancy and Similarity-weighted Greedy Algorithm with Redundancy to enhance the performance. Time simulations using known coronavirus genomes deposited as early as 10 years prior to the COVID-19 outbreak show that at least three SARS-CoV-2-targeting siRNAs are among the top 30 pre-designed siRNAs. In addition, among the top 19 pre-designed gRNAs, there are three SARS-CoV-2-targeting Cas13a gRNAs that could be predicted using information from 2011. Before-the-outbreak design is also possible against the MERS-CoV virus and the 2009-H1N1 swine flu virus. Designed siRNAs are further shown to suppress SARS-CoV-2 viral sequences using in vitro reporter assays. Our results support the utility of Evitar to pre-design anti-viral siRNAs/gRNAs against future viruses. Therefore, we propose the development of a collection consisting of roughly 30 pre-designed, safety-tested and off-the-shelf siRNA/CRISPR therapeutics that could accelerate responses to future RNA virus outbreaks. AVAILABILITY AND IMPLEMENTATION: Codes are available at GitHub (https://github.com/dingyaozhang/Evitar). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

COVID-19Influenza A Virus, H1N1 SubtypeAnimalsAntiviral AgentsPandemicsRNA, Small InterferingRNA, ViralSARS-CoV-2SwineAntiviral AgentsRNA, Small InterferingRNA, Viral

Identifiers

PMID35294970
PMCPMC9048652
OpenAlexW4220747460

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.