Evidence map›Paper›PMID 21445235›Full record

ArticlePLoS pathogens2011

Chemokine binding protein M3 of murine gammaherpesvirus 68 modulates the host response to infection in a natural host.

David J Hughes, Anja Kipar, Gail H Leeming, Elaine Bennett, Deborah Howarth, Joanne A Cummerson, Rita Papoula-Pereira, Brian F Flanagan, Jeffery T Sample, James P Stewart

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Biophysical and Computational Studies of the vCCI:vMIP-II Complex.International journal of molecular sciences · 2017
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Insights from natural host-parasite interactions: the Drosophila model.Developmental and comparative immunology · 2014
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

10 authors at 2 institutions in 2 countries.

David J HughesSchool of Infection and Host Defence, The University of Liverpool, Liverpool, United Kingdom.
Anja Kipar
Gail H Leeming
Elaine Bennett
Deborah Howarth
Joanne A Cummerson
Rita Papoula-Pereira
Brian F Flanagan
Jeffery T Sample
James P Stewart
University of Liverpool · GBPennsylvania State University · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Murine Model of Gammaherpesvirus LatencyR01CA090208 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SAMPLE, JEFFERY T · 2001 to 2005
$1.4M
NCI NIH HHS CA090208NCI NIH HHS CA21765NCI NIH HHS P30 CA021765NCI NIH HHS R01 CA090208
6 · The paper itself

Abstract

Murine γ-herpesvirus 68 (MHV-68) infection of Mus musculus-derived strains of mice is an attractive model of γ-herpesvirus infection. Surprisingly, however, ablation of expression of MHV-68 M3, a secreted protein with broad chemokine-binding properties in vitro, has no discernable effect during experimental infection via the respiratory tract. Here we demonstrate that M3 indeed contributes significantly to MHV-68 infection, but only in the context of a natural host, the wood mouse (Apodemus sylvaticus). Specifically, M3 was essential for two features unique to the wood mouse: virus-dependent inducible bronchus-associated lymphoid tissue (iBALT) in the lung and highly organized secondary follicles in the spleen, both predominant sites of latency in these organs. Consequently, lack of M3 resulted in substantially reduced latency in the spleen and lung. In the absence of M3, splenic germinal centers appeared as previously described for MHV-68-infected laboratory strains of mice, further evidence that M3 is not fully functional in the established model host. Finally, analyses of M3's influence on chemokine and cytokine levels within the lungs of infected wood mice were consistent with the known chemokine-binding profile of M3, and revealed additional influences that provide further insight into its role in MHV-68 biology.

Indexed as

AnimalsBronchiCell LineChemokinesCricetinaeGammaherpesvirinaeHerpesviridae InfectionsLungLymphoid TissueMiceMurinaeSpleenViral ProteinsVirus LatencyChemokinesM3 protein, Murine gammaherpesvirusViral Proteins

Identifiers

PMID21445235
PMCPMC3060169
OpenAlexW2031317532

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.