Evidence map›Paper›PMID 26202230›Full record

ArticleJournal of virology2015

Temporal Characterization of Marburg Virus Angola Infection following Aerosol Challenge in Rhesus Macaques.

Kenny L Lin, Nancy A Twenhafel, John H Connor, Kathleen A Cashman, Joshua D Shamblin, Ginger C Donnelly, Heather L Esham, Carly B Wlazlowski, Joshua C Johnson, Anna N Honko and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.5field-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

23 citing papers in PubMed, 30 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

14 authors at 3 institutions in 1 country.

Kenny L LinUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Nancy A TwenhafelUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
John H ConnorBoston University School of Medicine and National Emerging Infectious Diseases Laboratory, Boston, Massachusetts, USA.
Kathleen A CashmanUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Joshua D ShamblinUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Ginger C DonnellyUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Heather L EshamUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Carly B WlazlowskiUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Joshua C JohnsonUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA Integrated Research Facility, National Institute of Allergy and Infectious Diseases, Fort Detrick, Maryland, USA.
Anna N HonkoUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA Integrated Research Facility, National Institute of Allergy and Infectious Diseases, Fort Detrick, Maryland, USA.
Miriam A BottoUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Judy YenBoston University School of Medicine and National Emerging Infectious Diseases Laboratory, Boston, Massachusetts, USA.
Lisa E HensleyUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA Integrated Research Facility, National Institute of Allergy and Infectious Diseases, Fort Detrick, Maryland, USA.
Arthur J GoffUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA arthur.j.goff.civ@mail.mil.
United States Army Medical Research Institute of Infectious Diseases · USNational Institute of Allergy and Infectious Diseases · USBoston University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledMarburg virus (MARV) infection is a lethal hemorrhagic fever for which no licensed vaccines or therapeutics are available. Development of appropriate medical countermeasures requires a thorough understanding of the interaction between the host and the pathogen and the resulting disease course. In this study, 15 rhesus macaques were sequentially sacrificed following aerosol exposure to the MARV variant Angola, with longitudinal changes in physiology, immunology, and histopathology used to assess disease progression. Immunohistochemical evidence of infection and resulting histopathological changes were identified as early as day 3 postexposure (p.e.). The appearance of fever in infected animals coincided with the detection of serum viremia and plasma viral genomes on day 4 p.e. High (>10(7) PFU/ml) viral loads were detected in all major organs (lung, liver, spleen, kidney, brain, etc.) beginning day 6 p.e. Clinical pathology findings included coagulopathy, leukocytosis, and profound liver destruction as indicated by elevated liver transaminases, azotemia, and hypoalbuminemia. Altered cytokine expression in response to infection included early increases in Th2 cytokines such as interleukin 10 (IL-10) and IL-5 and late-stage increases in Th1 cytokines such as IL-2, IL-15, and granulocyte-macrophage colony-stimulating factor (GM-CSF). This study provides a longitudinal examination of clinical disease of aerosol MARV Angola infection in the rhesus macaque model. IMPORTANCE: In this study, we carefully analyzed the timeline of Marburg virus infection in nonhuman primates in order to provide a well-characterized model of disease progression following aerosol exposure.

Indexed as

Host-Pathogen InteractionsAerosolsAnimalsCytokinesDisease ProgressionImmunohistochemistryLongitudinal StudiesMacaca mulattaMarburgvirusMarburg Virus DiseaseTime FactorsViral LoadAerosolsCytokines

Identifiers

PMID26202230
PMCPMC4577920
OpenAlexW1892150725

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.