Evidence map›Paper›PMID 28852031›Full record

ArticleScientific reports2017

Infection with the Makona variant results in a delayed and distinct host immune response compared to previous Ebola virus variants.

Krista Versteeg, Andrea R Menicucci, Courtney Woolsey, Chad E Mire, Joan B Geisbert, Robert W Cross, Krystle N Agans, Daniel Jeske, Ilhem Messaoudi, Thomas W Geisbert

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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 12% 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.

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  5. Recent Advances in Therapeutic Approaches Against Ebola Virus Infection.Recent advances in anti-infective drug discovery · 2024
    Review
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  10. Extracellular vesicle storm during the course of Ebola virus infection in primates.Frontiers in cellular and infection microbiology · 2023
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. mBio · 2021
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Krista VersteegGalveston National Laboratory, Galveston, TX, USA.
Andrea R MenicucciDivision of Biomedical Sciences, University of California-Riverside, Riverside, CA, USA.
Courtney WoolseyGalveston National Laboratory, Galveston, TX, USA.
Chad E MireGalveston National Laboratory, Galveston, TX, USA.ORCID http://orcid.org/0000-0001-7596-1808
Joan B GeisbertGalveston National Laboratory, Galveston, TX, USA.
Robert W CrossGalveston National Laboratory, Galveston, TX, USA.
Krystle N AgansGalveston National Laboratory, Galveston, TX, USA.ORCID http://orcid.org/0000-0002-7319-6935
Daniel JeskeDivision of Biomedical Sciences, University of California-Riverside, Riverside, CA, USA.
Ilhem MessaoudiDepartment of Molecular Biology and Biochemistry, University of California-Irvine, Irvine, CA, USA. imessaou@uci.edu.
Thomas W GeisbertGalveston National Laboratory, Galveston, TX, USA. twgeisbe@utmb.edu.
Galveston College · USUniversity of California, Riverside · USUniversity of California, Irvine · US

Funding

Molecular mechanisms of immune dysregulation by filoviral interferon U19AI109945 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BASLER, CHRISTOPHER F · 2014 to 2018
$9.5M
NIAID NIH HHS U19 AI109945
6 · The paper itself

Abstract

Zaire Ebolavirus (ZEBOV) continues to pose a significant threat to human health as highlighted by the recent epidemic that originated in West Africa and the ongoing outbreak in the Democratic Republic of the Congo. Although the ZEBOV variant responsible for this epidemic (Makona) shares significant genetic similarity with previously identified variants (Kikwit and Mayinga), recent reports suggest slower disease progression in nonhuman primates. However, the pathogenesis caused by the new variant is not fully understood. We present the first comprehensive approach in understanding ZEBOV-Makona pathogenesis in cynomolgus macaques by measuring changes in immune cell frequencies, plasma levels of immune mediators, and differentially expressed genes (DEGs) within whole blood (WB) and peripheral blood mononuclear cells (PBMC). Our combined approach revealed a link between: 1) increased interferon-stimulated gene expression, IFNα levels, and activated plasmacytoid dendritic cells; 2) higher proinflammatory gene expression, cytokine and chemokine levels, and non-classical monocytes; 3) gene signature of leukocyte activation and increased granulocytes; and 4) decreased expression of lymphocyte related genes and lymphopenia. In addition, our data strongly indicate delayed disease progression as well as limited overlap (~30%) in host transcriptome changes following ZEBOV-Makona infection compared to ZEBOV-Kikwit. These observations provide novel insight into the molecular mechanisms of ZEBOV-Makona pathogenesis.

Indexed as

AnimalsBiomarkersDemocratic Republic of the CongoEbolavirusGene Expression ProfilingGene Regulatory NetworksHemorrhagic Fever, EbolaHost-Pathogen InteractionsHumansImmunity, InnateImmunomodulationLeukocytes, MononuclearLymphocyte ActivationLymphopeniaMacaca fascicularisOxidative StressBiomarkers

Identifiers

PMID28852031
PMCPMC5574898
OpenAlexW2746006953

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.