Evidence map›Paper›PMID 33374514›Full record

ArticleViruses2020

Fluoroquinolone Antibiotics Exhibit Low Antiviral Activity against SARS-CoV-2 and MERS-CoV.

Stacey L P Scroggs, Danielle K Offerdahl, Dylan P Flather, Ciera N Morris, Benjamin L Kendall, Rebecca M Broeckel, Paul A Beare, Marshall E Bloom

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.9field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 45 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Stacey L P ScroggsBiology of Vector-Borne Viruses Section, Laboratory of Virology, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA.ORCID 0000-0003-1882-2697
Danielle K OfferdahlBiology of Vector-Borne Viruses Section, Laboratory of Virology, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA.ORCID 0000-0002-0736-1664
Dylan P FlatherBiology of Vector-Borne Viruses Section, Laboratory of Virology, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA.ORCID 0000-0003-3268-5385
Ciera N MorrisBiology of Vector-Borne Viruses Section, Laboratory of Virology, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA.
Benjamin L KendallBiology of Vector-Borne Viruses Section, Laboratory of Virology, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA.
Rebecca M BroeckelInnate Immunity and Pathogenesis Section Laboratory of Virology, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA.
Paul A BeareCoxiella Pathogenesis Section, Laboratory of Bacteriology, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA.
Marshall E BloomBiology of Vector-Borne Viruses Section, Laboratory of Virology, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA.ORCID 0000-0001-7003-2313
National Institutes of Health · US

Funding

NIH HHS Intramural Research Program of the National Institute of Allergy and Infectious Diseases
6 · The paper itself

Abstract

Repurposing FDA-approved drugs that treat respiratory infections caused by coronaviruses, such as SARS-CoV-2 and MERS-CoV, could quickly provide much needed antiviral therapies. In the current study, the potency and cellular toxicity of four fluoroquinolones (enoxacin, ciprofloxacin, levofloxacin, and moxifloxacin) were assessed in Vero cells and A549 cells engineered to overexpress ACE2, the SARS-CoV-2 entry receptor. All four fluoroquinolones suppressed SARS-CoV-2 replication at high micromolar concentrations in both cell types, with enoxacin demonstrating the lowest effective concentration 50 value (EC

Indexed as

COVID-19 Drug TreatmentA549 CellsAngiotensin-Converting Enzyme 2AnimalsAnti-Bacterial AgentsAntiviral AgentsCell LineChlorocebus aethiopsCiprofloxacinCoronavirus InfectionsEnoxacinFluoroquinolonesHumansLevofloxacinMiddle East Respiratory Syndrome CoronavirusMoxifloxacinACE2 protein, humanAngiotensin-Converting Enzyme 2Anti-Bacterial AgentsAntiviral AgentsCiprofloxacinEnoxacinFluoroquinolonesLevofloxacinMoxifloxacinantiviralciprofloxacinCovid-19efficacyenoxacinfluoroquinoloneslevofloxacinMERSmoxifloxacinSARS-CoV-2

Identifiers

PMID33374514
PMCPMC7822115
OpenAlexW3114040933

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.