Evidence map›Paper›PMID 26150505›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Limits and patterns of cytomegalovirus genomic diversity in humans.

Nicholas Renzette, Cornelia Pokalyuk, Laura Gibson, Bornali Bhattacharjee, Mark R Schleiss, Klaus Hamprecht, Aparecida Y Yamamoto, Marisa M Mussi-Pinhata, William J Britt, Jeffrey D Jensen and 1 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

77 citing papers in PubMed, 123 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. A vaccine against cytomegalovirus: how close are we?The Journal of clinical investigation · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Genomic and geographical structure of human cytomegalovirus.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Variants of HCMVInternational journal of molecular sciences · 2022
    Article
  18. Article
  19. Article
  20. Article

17 more citing papers are in PubMed but not listed here.

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

11 authors at 6 institutions in 4 countries.

Nicholas RenzetteDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA 01655;
Cornelia PokalyukInstitute for Stochastics, Goethe Universität Frankfurt, D-60325 Frankfurt am Main, Germany; Swiss Institute of Bioinformatics, 1015 Lausanne, Switzerland;
Laura GibsonDepartment of Pediatrics, University of Massachusetts Medical School, Worcester, MA 01605; Division of Infectious Diseases and Immunology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01655;
Bornali BhattacharjeeDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA 01655;
Mark R SchleissCenter for Infectious Diseases and Microbiology Translational Research, University of Minnesota Medical School, Minneapolis, MN 55455; Division of Pediatric Infectious Diseases, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN 55455;
Klaus HamprechtInstitute for Medical Virology, University Hospital Tübingen, 72076 Tübingen, Germany;
Aparecida Y YamamotoDepartment of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto-São Paulo 14048-900, Brazil;
Marisa M Mussi-PinhataDepartment of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto-São Paulo 14048-900, Brazil;
William J BrittDepartment of Pediatrics, University of Alabama Birmingham School of Medicine, Birmingham, AL 35294;
Jeffrey D JensenSwiss Institute of Bioinformatics, 1015 Lausanne, Switzerland; School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland; Timothy.Kowalik@umassmed.edu jeffrey.jensen@epfl.ch.
Timothy F KowalikDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA 01655; Immunology and Virology Program, University of Massachusetts Medical School, Worcester, MA 01655 Timothy.Kowalik@umassmed.edu jeffrey.jensen@epfl.ch.
University of Massachusetts Chan Medical School · USUniversidade de São Paulo · BRGoethe University Frankfurt · DESIB Swiss Institute of Bioinformatics · CHUniversity of Alabama at Birmingham · USUniversity of Minnesota Medical Center · US

Funding

University of Massachusetts Center for Clinical and Translational ScienceUL1TR000161 · NCATS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LUZURIAGA, KATHERINE F · 2012 to 2015
$11.0M
CMV Vaccines: Reinfection and Antigenic Variation (Vision and auditory screening in infants born to women enrolled in ZIP)R01HD061959 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BRITT, WILLIAM JARVIS, MUSSI-PINHATA, MARISA MARCIA · 2011 to 2023
$5.9M
Acquisition of HCMV from breast milk-correlates of protectionR01AI109001 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BOPPANA, SURESH B · 2014 to 2017
$2.8M
Genomic Variability of Cytomegalovirus in a Clinical SettingF32AI084437 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI RENZETTE, NICHOLAS · 2009 to 2010
$93k
NCATS NIH HHS UL1 TR000161NCATS NIH HHS UL1TR000161NIAID NIH HHS AI109001NIAID NIH HHS F32 AI084437NIAID NIH HHS F32AI084437NIAID NIH HHS R01 AI109001NICHD NIH HHS HD061959NICHD NIH HHS R01 HD061959
6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) exhibits surprisingly high genomic diversity during natural infection although little is known about the limits or patterns of HCMV diversity among humans. To address this deficiency, we analyzed genomic diversity among congenitally infected infants. We show that there is an upper limit to HCMV genomic diversity in these patient samples, with ∼ 25% of the genome being devoid of polymorphisms. These low diversity regions were distributed across 26 loci that were preferentially located in DNA-processing genes. Furthermore, by developing, to our knowledge, the first genome-wide mutation and recombination rate maps for HCMV, we show that genomic diversity is positively correlated with these two rates. In contrast, median levels of viral genomic diversity did not vary between putatively single or mixed strain infections. We also provide evidence that HCMV populations isolated from vascular compartments of hosts from different continents are genetically similar and that polymorphisms in glycoproteins and regulatory proteins are enriched in these viral populations. This analysis provides the most highly detailed map of HCMV genomic diversity in human hosts to date and informs our understanding of the distribution of HCMV genomic diversity within human hosts.

Indexed as

Genetic VariationGenome, ViralCluster AnalysisCytomegalovirusCytomegalovirus InfectionsEvolution, MolecularGene Expression RegulationGenes, ViralGenomicsGlycoproteinsHumansInfantInfant, NewbornMutationPolymorphism, GeneticRecombination, GeneticGlycoproteinscongenital CMVevolutionHCMVhuman cytomegalovirusvirology

Identifiers

PMID26150505
PMCPMC4522815
OpenAlexW1773931763

What OpenQuestion holds

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Registered trials

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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.