Evidence map›Paper›PMID 27161622›Full record

ArticleAntimicrobial agents and chemotherapy2016

Large-Scale Screening and Identification of Novel Ebola Virus and Marburg Virus Entry Inhibitors.

Manu Anantpadma, Jennifer Kouznetsova, Hang Wang, Ruili Huang, Andrey Kolokoltsov, Rajarshi Guha, Aaron R Lindstrom, Olena Shtanko, Anton Simeonov, David J Maloney and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2016. 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
6.5field-weighted citation impact, top 3% 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, 54 citations in OpenAlex.

  1. Article
  2. Ebola virus exploits host lncRNAbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Virus Entry Inhibitors: Past, Present, and Future.Advances in experimental medicine and biology · 2022
    Review
  11. Article
  12. Article
  13. Host-Directed Antiviral Therapy.Clinical microbiology reviews · 2020
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review
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

14 authors at 6 institutions in 1 country.

Manu AnantpadmaDepartment of Virology and Immunology, Texas Biomedical Research Institute, San Antonio, Texas, USA.
Jennifer KouznetsovaNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.
Hang WangNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.
Ruili HuangNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.
Andrey KolokoltsovDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, USA.
Rajarshi GuhaNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.
Aaron R LindstromDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana, USA.
Olena ShtankoDepartment of Virology and Immunology, Texas Biomedical Research Institute, San Antonio, Texas, USA.
Anton SimeonovNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.
David J MaloneyNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.
Wendy MauryDepartment of Microbiology, University of Iowa, Iowa City, Iowa, USA.
Douglas J LaCountDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana, USA.
Ajit JadhavNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.
Robert A DaveyDepartment of Virology and Immunology, Texas Biomedical Research Institute, San Antonio, Texas, USA rdavey@txbiomed.org.
National Center for Advancing Translational Sciences · USNational Institutes of Health · USTexas Biomedical Research Institute · USPurdue University West Lafayette · USThe University of Texas Medical Branch at Galveston · USUniversity of Iowa · US

Funding

Small molecule screening programZ01HG200319 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI AUSTIN, CHRISTOPHER P · 2004 to 2008
$32.3M
Emerging virus-host cell protein interaction networksR01AI114814 · NIAID · PURDUE UNIVERSITY · PI DAVEY, ROBERT A, LACOUNT, DOUGLAS J. · 2015 to 2019
$3.5M
Filoviral glycoprotein/cellular protein interactionsR01AI077519 · NIAID · UNIVERSITY OF IOWA · PI MAURY, WENDY JEAN · 2010 to 2014
$1.7M
Novel broad spectrum inhibitors of filovirus infectionR21AI115082 · NIAID · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI DAVEY, ROBERT A · 2015 to 2016
$509k
HTS for Filo- and Arena-virus Entry MechanismsR03MH086850 · NIMH · UNIVERSITY OF TEXAS MED BR GALVESTON · PI DAVEY, ROBERT A · 2009 to 2010
$75k
Intramural NIH HHS Z01 HG200319NIAID NIH HHS R01 AI077519NIAID NIH HHS R01 AI114814NIAID NIH HHS R21 AI115082NIMH NIH HHS R03 MH086850
6 · The paper itself

Abstract

Filoviruses are highly infectious, and no FDA-approved drug therapy for filovirus infection is available. Most work to find a treatment has involved only a few strains of Ebola virus and testing of relatively small drug libraries or compounds that have shown efficacy against other virus types. Here we report the findings of a high-throughput screening of 319,855 small molecules from the Molecular Libraries Small Molecule Repository library for their activities against Marburg virus and Ebola virus. Nine of the most potent, novel compounds that blocked infection by both viruses were analyzed in detail for their mechanisms of action. The compounds inhibited known key steps in the Ebola virus infection mechanism by blocking either cell surface attachment, macropinocytosis-mediated uptake, or endosomal trafficking. To date, very few specific inhibitors of macropinocytosis have been reported. The 2 novel macropinocytosis inhibitors are more potent inhibitors of Ebola virus infection and less toxic than ethylisopropylamiloride, one commonly accepted macropinocytosis inhibitor. Each compound blocked infection of primary human macrophages, indicating their potential to be developed as new antifiloviral therapies.

Indexed as

AnimalsAntiviral AgentsCell LineChlorocebus aethiopsEbolavirusHeLa CellsHumansMarburgvirusVero CellsAntiviral Agents

Identifiers

PMID27161622
PMCPMC4958205
OpenAlexW2346312782

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.