Evidence map›Paper›PMID 16971451›Full record

ArticleJournal of virology2006

hsp72, a host determinant of measles virus neurovirulence.

Thomas Carsillo, Zachary Traylor, Changsun Choi, Stefan Niewiesk, Michael Oglesbee

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Review
  3. Chaperoning theViruses · 2018
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
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  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Blue moon neurovirology: the merits of studying rare CNS diseases of viral origin.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2010
    Review
  17. Article
  18. Article
  19. Making it to the synapse: measles virus spread in and among neurons.Current topics in microbiology and immunology · 2009
    Review
  20. Article
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

5 authors at 2 institutions in 2 countries.

Thomas CarsilloDepartment of Veterinary Biosciences, The Ohio State University, 1925 Coffey Road, Columbus, OH 43210, USA.
Zachary Traylor
Changsun Choi
Stefan Niewiesk
Michael Oglesbee
The Ohio State University · USChung-Ang University · KR

Funding

THE CELLULAR STRESS RESPONSE IN VIRAL ENCEPHALITISR01NS031693 · NINDS · OHIO STATE UNIVERSITY · PI OGLESBEE, MICHAEL J · 2000 to 2008
$1.8M
NINDS NIH HHS R01 NS031693NINDS NIH HHS R01NS31693
6 · The paper itself

Abstract

Transient hyperthermia such as that experienced during febrile episodes increases expression of the major inducible 70-kDa heat shock protein (hsp72). Despite the relevance of febrile episodes to viral pathogenesis and the multiple in vitro roles of heat shock proteins in viral replication and gene expression, the in vivo significance of virus-heat shock protein interactions is unknown. The present work determined the in vivo relationship between hsp72 levels and neurovirulence of an hsp72-responsive virus using the mouse model of measles virus (MV) encephalitis. Transgenic C57BL/6 mice were created to constitutively overexpress hsp72 in neurons, and these mice were inoculated intracranially with Edmonston MV (Ed MV) at 42 h of age. The mean viral RNA burden in brain was approximately 2 orders of magnitude higher in transgenic animals than in nontransgenic animals 2 to 4 weeks postinfection, and this increased burden was associated with a fivefold increase in mortality. Mice were also challenged with an Ed MV variant exhibiting an attenuated in vitro response to hsp72-dependent stimulation of viral transcription (Ed N-522D). This virus exhibited an attenuated neuropathogenicity in transgenic mice, where mortality and viral RNA burdens were not significantly different from nontransgenic mice infected with either Ed N-522D or parent Ed MV. Collectively, these results indicate that hsp72 levels can serve as a host determinant of viral neurovirulence in C57BL/6 mice, reflecting the direct influence of hsp72 on viral gene expression.

Indexed as

VirulenceAnimalsBrainDisease Models, AnimalEncephalitis, ViralFemaleGene ExpressionHistocytochemistryHSP72 Heat-Shock ProteinsMaleMeaslesMeasles virusMiceMice, Inbred C57BLMice, TransgenicRNA, ViralHSP72 Heat-Shock ProteinsRNA, Viral

Identifiers

PMID16971451
PMCPMC1642166
OpenAlexW2138391803

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.