Evidence map›Paper›PMID 23935483›Full record

ArticlePLoS pathogens2013

The viral chemokine MCK-2 of murine cytomegalovirus promotes infection as part of a gH/gL/MCK-2 complex.

Felicia M Wagner, Ilija Brizic, Adrian Prager, Tihana Trsan, Maja Arapovic, Niels A W Lemmermann, Jürgen Podlech, Matthias J Reddehase, Frederic Lemnitzer, Jens Bernhard Bosse and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

58 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Article
  3. Immune surveillance of cytomegalovirus in tissues.Cellular & molecular immunology · 2024
    Review
  4. Article
  5. Article
  6. Oncolytic α-herpesvirus and myeloid-tropic cytomegalovirus cooperatively enhance systemic antitumor responses.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. MCMV Centrifugal Enhancement: A New Spin on an Old Topic.Pathogens (Basel, Switzerland) · 2021
    Article
  15. Article
  16. Murine Cytomegalovirus MCK-2 FacilitatesJournal of virology · 2021
    Article
  17. Review
  18. Article
  19. Article
  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

16 authors at 6 institutions in 3 countries.

Felicia M WagnerMax von Pettenkofer-Institute for Virology, Ludwig-Maximilians-University Munich, Munich, Germany.
Ilija Brizic
Adrian Prager
Tihana Trsan
Maja Arapovic
Niels A W Lemmermann
Jürgen Podlech
Matthias J Reddehase
Frederic Lemnitzer
Jens Bernhard Bosse
Martina Gimpfl
Lisa Marcinowski
Margaret MacDonald
Heiko Adler
Ulrich H Koszinowski
Barbara Adler
Ludwig-Maximilians-Universität München · DEUniversity Medical Center of the Johannes Gutenberg University Mainz · DEUniversity of Rijeka · HRHelmholtz Zentrum München · DEJohannes Gutenberg University Mainz · DERockefeller University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) forms two gH/gL glycoprotein complexes, gH/gL/gO and gH/gL/pUL(128,130,131A), which determine the tropism, the entry pathways and the mode of spread of the virus. For murine cytomegalovirus (MCMV), which serves as a model for HCMV, a gH/gL/gO complex functionally homologous to the HCMV gH/gL/gO complex has been described. Knock-out of MCMV gO does impair, but not abolish, virus spread indicating that also MCMV might form an alternative gH/gL complex. Here, we show that the MCMV CC chemokine MCK-2 forms a complex with the glycoprotein gH, a complex which is incorporated into the virion. We could additionally show that mutants lacking both, gO and MCK-2 are not able to produce infectious virus. Trans-complementation of these double mutants with either gO or MCK-2 showed that both proteins can promote infection of host cells, although through different entry pathways. MCK-2 has been extensively studied in vivo by others. It has been shown to be involved in attracting cells for virus dissemination and in regulating antiviral host responses. We now show that MCK-2, by forming a complex with gH, strongly promotes infection of macrophages in vitro and in vivo. Thus, MCK-2 may play a dual role in MCMV infection, as a chemokine regulating the host response and attracting specific target cells and as part of a glycoprotein complex promoting entry into cells crucial for virus dissemination.

Indexed as

Immunity, InnateVirus InternalizationAnimalsCell LineCells, CulturedChemokines, CCFemaleHerpesviridae InfectionsLiverMacrophagesMacrophages, PeritonealMiceMice, Inbred BALB CMuromegalovirusMutationProtein MultimerizationChemokines, CCMCK-2 protein, Mouse cytomegalovirus 1Recombinant ProteinsViral Envelope ProteinsViral Proteins

Identifiers

PMID23935483
PMCPMC3723581
OpenAlexW2012102254

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.