Evidence map›Paper›PMID 32966040›Full record

ArticleACS infectious diseases2021

Targeting Polyamines Inhibits Coronavirus Infection by Reducing Cellular Attachment and Entry.

Mason R Firpo, Vincent Mastrodomenico, Grant M Hawkins, Matthieu Prot, Laura Levillayer, Tom Gallagher, Etienne Simon-Loriere, Bryan C Mounce

Open access · bronzeAbstract read
In one paragraph

Article in ACS infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  3. Host metabolic responses to SARS-CoV-2 and influenza viruses: parallels and contrasts.Metabolomics : Official journal of the Metabolomic Society · 2026
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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 2 institutions in 2 countries.

Mason R FirpoDepartment of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois 60153, United States.
Vincent MastrodomenicoDepartment of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois 60153, United States.
Grant M HawkinsDepartment of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois 60153, United States.
Matthieu ProtG5 Evolutionary Genomics of RNA Viruses, Institut Pasteur, Paris 75015, France.
Laura LevillayerFunctional Genetics of Infectious Diseases Unit, Institut Pasteur, Paris 75015, France.
Tom GallagherDepartment of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois 60153, United States.ORCID 0000-0002-8601-5961
Etienne Simon-LoriereG5 Evolutionary Genomics of RNA Viruses, Institut Pasteur, Paris 75015, France.
Bryan C MounceDepartment of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois 60153, United States.ORCID 0000-0003-1710-5362
Loyola University Chicago · USInstitut Pasteur · FR

Funding

Experimental Immunology Training GrantT32AI007508 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI KNIGHT, KATHERINE L. · 1997 to 2022
$4.0M
Uncovering and harnessing connected metabolic pathways essential to virus infection.R35GM138199 · NIGMS · LOYOLA UNIVERSITY CHICAGO · PI Bryan C Mounce · 2020 to 2026
$2.7M
NIAID NIH HHS T32 AI007508NIGMS NIH HHS R35 GM138199
6 · The paper itself

Abstract

Coronaviruses first garnered widespread attention in 2002 when the severe acute respiratory syndrome coronavirus (SARS-CoV) emerged from bats in China and rapidly spread in human populations. Since then, Middle East respiratory syndrome coronavirus (MERS-CoV) emerged and still actively infects humans. The recent SARS-CoV-2 outbreak and the resulting disease (coronavirus disease 2019, COVID19) have rapidly and catastrophically spread and highlighted significant limitations to our ability to control and treat infection. Thus, a basic understanding of entry and replication mechanisms of coronaviruses is necessary to rationally evaluate potential antivirals. Here, we show that polyamines, small metabolites synthesized in human cells, facilitate coronavirus replication and the depletion of polyamines with FDA-approved molecules significantly reduces coronavirus replication. We find that diverse coronaviruses, including endemic and epidemic coronaviruses, exhibit reduced attachment and entry into polyamine-depleted cells. We further demonstrate that several molecules targeting the polyamine biosynthetic pathway are antiviral

Indexed as

COVID-19Middle East Respiratory Syndrome CoronavirusAntiviral AgentsHumansPolyaminesSARS-CoV-2Antiviral AgentsPolyaminesbindingcoronaviruspolyaminesSARS-CoV-2

Identifiers

PMID32966040
PMCPMC7539557
OpenAlexW3087399655

What OpenQuestion holds

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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.