Evidence map›Paper›PMID 27147733›Full record

ArticleJournal of virology2016

Nipah Virus C and W Proteins Contribute to Respiratory Disease in Ferrets.

Benjamin A Satterfield, Robert W Cross, Karla A Fenton, Viktoriya Borisevich, Krystle N Agans, Daniel J Deer, Jessica Graber, Christopher F Basler, Thomas W Geisbert, Chad E Mire

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Journal of virology, 2016. 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 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

40 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Benjamin A SatterfieldGalveston National Laboratory, University of Texas Medical Branch, Galveston, Texas, USA.
Robert W CrossGalveston National Laboratory, University of Texas Medical Branch, Galveston, Texas, USA.
Karla A FentonGalveston National Laboratory, University of Texas Medical Branch, Galveston, Texas, USA.
Viktoriya BorisevichGalveston National Laboratory, University of Texas Medical Branch, Galveston, Texas, USA.
Krystle N AgansGalveston National Laboratory, University of Texas Medical Branch, Galveston, Texas, USA.
Daniel J DeerGalveston National Laboratory, University of Texas Medical Branch, Galveston, Texas, USA.
Jessica GraberGalveston National Laboratory, University of Texas Medical Branch, Galveston, Texas, USA.
Christopher F BaslerDepartment of Microbiology, Mount Sinai School of Medicine, New York, New York, USA.
Thomas W GeisbertGalveston National Laboratory, University of Texas Medical Branch, Galveston, Texas, USA twgeisbe@utmb.edu.
Chad E MireGalveston National Laboratory, University of Texas Medical Branch, Galveston, Texas, USA.
The University of Texas Medical Branch at Galveston · USIcahn School of Medicine at Mount Sinai · US

Funding

Regulatory Compliance Core - Galveston National Laboratory BSL4 OperationsUC7AI094660 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI Dennis A Bente · 2011 to 2026
$208.8M
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
Nipah & Hendra Virus Nonhuman Primate Model & Therapeutics DevelopmentU01AI082121 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI GEISBERT, THOMAS WILLIAM · 2009 to 2013
$5.9M
NIAID NIH HHS U01 AI082121NIAID NIH HHS U19 AI109945NIAID NIH HHS UC7 AI094660
6 · The paper itself

Abstract

unlabelledNipah virus (NiV) is a highly lethal paramyxovirus that recently emerged as a causative agent of febrile encephalitis and severe respiratory disease in humans. The ferret model has emerged as the preferred small-animal model with which to study NiV disease, but much is still unknown about the viral determinants of NiV pathogenesis, including the contribution of the C protein in ferrets. Additionally, studies have yet to examine the synergistic effects of the various P gene products on pathogenesis in animal models. Using recombinant NiVs (rNiVs), we examine the sole contribution of the NiV C protein and the combined contributions of the C and W proteins in the ferret model of NiV pathogenesis. We show that an rNiV void of C expression resulted in 100% mortality, though with limited respiratory disease, like our previously reported rNiV void of W expression; this finding is in stark contrast to the attenuated phenotype observed in previous hamster studies utilizing rNiVs void of C expression. We also observed that an rNiV void of both C and W expression resulted in limited respiratory disease; however, there was severe neurological disease leading to 60% mortality, and the surviving ferrets demonstrated sequelae similar to those for human survivors of NiV encephalitis. IMPORTANCE: Nipah virus (NiV) is a human pathogen capable of causing lethal respiratory and neurological disease. Many human survivors have long-lasting neurological impairment. Using a ferret model, this study demonstrated the roles of the NiV C and W proteins in pathogenesis, where lack of either the C or the W protein independently decreased the severity of clinical respiratory disease but did not decrease lethality. Abolishing both C and W expression, however, dramatically decreased the severity of respiratory disease and the level of destruction of splenic germinal centers. These ferrets still suffered severe neurological disease: 60% succumbed to disease, and the survivors experienced long-term neurological impairment, such as that seen in human survivors. This new ferret NiV C and W knockout model may allow, for the first time, the examination of interventions to prevent or mitigate the neurological damage and sequelae experienced by human survivors.

Indexed as

AnimalsAntibodies, ViralCells, CulturedChlorocebus aethiopsCricetinaeEndothelium, VascularFemaleFerretsHenipavirus InfectionsHumansNipah VirusPhosphoproteinsRespiratory Tract DiseasesVero CellsViral LoadViral ProteinsAntibodies, ViralC protein, Nipah virusPhosphoproteinsViral ProteinsW protein, Nipah virus

Identifiers

PMID27147733
PMCPMC4936148
OpenAlexW2346586129

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.