Evidence map›Paper›PMID 31801842›Full record

ArticlemSphere2019

Rousette Bat Dendritic Cells Overcome Marburg Virus-Mediated Antiviral Responses by Upregulation of Interferon-Related Genes While Downregulating Proinflammatory Disease Mediators.

Joseph Prescott, Jonathan C Guito, Jessica R Spengler, Catherine E Arnold, Amy J Schuh, Brian R Amman, Tara K Sealy, Lisa W Guerrero, Gustavo F Palacios, Mariano Sanchez-Lockhart and 2 more

Open access · goldAbstract read
In one paragraph

Article in mSphere, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Chiropteran (Animals : an open access journal from MDPI · 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

12 authors at 2 institutions in 2 countries.

Joseph PrescottCenter for Biological Threats and Special Pathogens, Robert Koch Institute, Berlin, Germany prescottj@rki.de jit8@cdc.gov.
Jonathan C GuitoViral Special Pathogens Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Jessica R SpenglerViral Special Pathogens Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.ORCID 0000-0002-5383-0513
Catherine E ArnoldDiagnostic Systems Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Amy J SchuhViral Special Pathogens Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Brian R AmmanViral Special Pathogens Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Tara K SealyViral Special Pathogens Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Lisa W GuerreroViral Special Pathogens Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Gustavo F PalaciosCenter for Genome Sciences, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Mariano Sanchez-LockhartCenter for Genome Sciences, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Cesar G AlbariñoViral Special Pathogens Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Jonathan S TownerViral Special Pathogens Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, USA prescottj@rki.de jit8@cdc.gov.
Centers for Disease Control and Prevention · USUnited States Army Medical Research Institute of Infectious Diseases · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulated and maladaptive immune responses are at the forefront of human diseases caused by infection with zoonotic viral hemorrhagic fever viruses. Elucidating mechanisms of how the natural animal reservoirs of these viruses coexist with these agents without overt disease, while permitting sufficient replication to allow for transmission and maintenance in a population, is important for understanding the viral ecology and spillover to humans. The Egyptian rousette bat (ERB) has been identified as a reservoir for Marburg virus (MARV), a filovirus and the etiological agent of the highly lethal Marburg virus disease. Little is known regarding how these bats immunologically respond to MARV infection. In humans, macrophages and dendritic cells (DCs) are primary targets of infection, and their dysregulation is thought to play a central role in filovirus diseases, by disturbing their normal functions as innate sensors and adaptive immune response facilitators while serving as amplification and dissemination agents for the virus. The infection status and responses to MARV in bat myeloid-lineage cells are uncharacterized and likely represent an important modulator of the bat's immune response to MARV infection. Here, we generate DCs from the bone marrow of rousette bats. Infection with a bat isolate of MARV resulted in a low level of transcription in these cells and significantly downregulated DC maturation and adaptive immune-stimulatory pathways while simultaneously upregulating interferon-related pathogen-sensing pathways. This study provides a first insight into how the bat immune response is directed toward preventing aberrant inflammatory responses while mounting an antiviral response to defend against MARV infection.

Indexed as

Host-Pathogen InteractionsAnimalsCells, CulturedChiropteraDendritic CellsGene Expression RegulationImmunity, InnateImmunologic FactorsInterferonsMarburgvirusImmunologic FactorsInterferonsEbola virusimmune responseMarburg virusrousette batviral hemorrhagic fevervirology

Identifiers

PMID31801842
PMCPMC6893212
OpenAlexW2991706036

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.