Evidence map›Paper›PMID 15194765›Full record

ArticleJournal of virology2004

Murine cytomegalovirus with a transposon insertional mutation at open reading frame m155 is deficient in growth and virulence in mice.

Gerardo Abenes, Karen Chan, Manfred Lee, Erik Haghjoo, Jiaming Zhu, Tianhong Zhou, Xiaoyan Zhan, Fenyong Liu

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.8field-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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  4. Oral Vaccination with AttenuatedPathogens (Basel, Switzerland) · 2025
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  8. Effective inhibition of cytomegalovirus infection by external guide sequences in mice.Proceedings of the National Academy of Sciences of the United States of America · 2012
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  10. Oral delivery of RNase P ribozymes by Salmonella inhibits viral infection in mice.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  11. Article
  12. Effective inhibition in animals of viral pathogenesis by a ribozyme derived from RNase P catalytic RNA.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
  13. Article
  14. Murine cytomegalovirus encodes a stable intron that facilitates persistent replication in the mouse.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  15. Article
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  17. 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

8 authors at 1 institution in 1 country.

Gerardo AbenesDivision of Infectious Diseases, School of Public Health, University of California, Berkeley, 94720, USA.
Karen Chan
Manfred Lee
Erik Haghjoo
Jiaming Zhu
Tianhong Zhou
Xiaoyan Zhan
Fenyong Liu
University of California, Berkeley · US

Funding

TRAINING IN INFECTIOUS DISEASES AND IMMUNITY RESEARCH (T32 AI007620)T32AI007620 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI RILEY, LEE W · 2000 to 2010
$1.2M
NIAID NIH HHS T32 AI007620NIAID NIH HHS T32-AI007620
6 · The paper itself

Abstract

A pool of murine cytomegalovirus (MCMV) mutants was previously generated by using a Tn3-based transposon mutagenesis approach (X. Zhan, M. Lee, J. Xiao, and F. Liu, J. Virol. 74:7411-7421, 2000). In this study, one of the MCMV mutants, Rvm155, which contained the transposon insertion in open reading frame m155, was characterized in vitro for its replication in tissue culture and in vivo for its growth and virulence in immunodeficient SCID mice. Compared to the wild-type strain and a rescued virus that restored the m155 region, the mutant is significantly deficient in growth in many organs of the infected animals. At 21 days postinfection the titers of Rvm155 in the salivary glands, lungs, spleens, livers, and kidneys of the intraperitoneally infected SCID mice were lower than the titers of the wild-type virus and the rescued virus by 50-, 1,000-, 500-, 100-, and 500-fold, respectively. Moreover, the viral mutant was attenuated in killing the SCID mice, as none of the SCID mice that were intraperitoneally infected with Rvm155 died until 38 days postinfection while all the animals infected with the wild-type and rescued viruses died at 27 days postinfection. Our results provide the first direct evidence that a disruption of m155 expression leads to attenuation of viral virulence and growth in animals. Moreover, these results suggest that m155 is a viral determinant for optimal MCMV growth and virulence in vivo.

Indexed as

DNA Transposable ElementsMutagenesis, InsertionalAnimalsHerpesviridae InfectionsMiceMice, SCIDMuromegalovirusMutationNIH 3T3 CellsOpen Reading FramesViral ProteinsVirulenceVirus ReplicationDNA Transposable ElementsViral Proteins

Identifiers

PMID15194765
PMCPMC421665
OpenAlexW2156256798

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.