Evidence map›Paper›PMID 31050742›Full record

ArticleThe Journal of infectious diseases2019

Human Cytomegalovirus Genomes Sequenced Directly From Clinical Material: Variation, Multiple-Strain Infection, Recombination, and Gene Loss.

Nicolás M Suárez, Gavin S Wilkie, Elias Hage, Salvatore Camiolo, Marylouisa Holton, Joseph Hughes, Maha Maabar, Sreenu B Vattipally, Akshay Dhingra, Ursula A Gompels and 12 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
9.7field-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

84 citing papers in PubMed, 107 citations in OpenAlex.

  1. Review
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  5. Coinfection by multipleMicrobiology and molecular biology reviews : MMBR · 2025
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  15. The Pentamer glycoprotein complex inhibits viral Immediate Early transcription during Human Cytomegalovirus infections.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Immune surveillance of cytomegalovirus in tissues.Cellular & molecular immunology · 2024
    Review
  17. Review
  18. Article
  19. Article
  20. Review

24 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

22 authors at 9 institutions in 5 countries.

Nicolás M SuárezMedical Research Council-University of Glasgow Centre for Virus Research, United Kingdom.
Gavin S WilkieMedical Research Council-University of Glasgow Centre for Virus Research, United Kingdom.
Elias HageInstitute of Virology, Hannover Medical School, United Kingdom.
Salvatore CamioloMedical Research Council-University of Glasgow Centre for Virus Research, United Kingdom.
Marylouisa HoltonMedical Research Council-University of Glasgow Centre for Virus Research, United Kingdom.
Joseph HughesMedical Research Council-University of Glasgow Centre for Virus Research, United Kingdom.
Maha MaabarMedical Research Council-University of Glasgow Centre for Virus Research, United Kingdom.
Sreenu B VattipallyMedical Research Council-University of Glasgow Centre for Virus Research, United Kingdom.
Akshay DhingraInstitute of Virology, Hannover Medical School, United Kingdom.
Ursula A GompelsPathogen Molecular Biology Department, London School of Hygiene and Tropical Medicine, United Kingdom.
Gavin W G WilkinsonDivision of Infection and Immunity, School of Medicine, Cardiff University, United Kingdom.
Fausto BaldantiMolecular Virology Unit, Microbiology and Virology Department, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Italy.
Milena FurioneMolecular Virology Unit, Microbiology and Virology Department, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Italy.
Daniele LilleriLaboratory of Genetics-Transplantology and Cardiovascular Diseases, Italy.
Alessia ArossaDepartments of Obstetrics and Gynecology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Tina GanzenmuellerInstitute of Virology, Hannover Medical School, United Kingdom.
Giuseppe GernaLaboratory of Genetics-Transplantology and Cardiovascular Diseases, Italy.
Petr HubáčekDepartment of Medical Microbiology, Motol University Hospital, Prague, Czech Republic, Israel.
Thomas F SchulzInstitute of Virology, Hannover Medical School, United Kingdom.
Dana WolfClinical Virology Unit, Department of Clinical Microbiology and Infectious Diseases, Hadassah University Hospital, Jerusalem, Israel.
Maurizio ZavattoniMolecular Virology Unit, Microbiology and Virology Department, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Italy.
Andrew J DavisonMedical Research Council-University of Glasgow Centre for Virus Research, United Kingdom.
MRC University of Glasgow Centre for Virus Research · GBIstituti di Ricovero e Cura a Carattere Scientifico · ITCardiff University · GBHadassah Academic College · ILInstitute of Medical Microbiology and Hygiene · DEPoliclinico San Matteo Fondazione · ITUniversity Hospital in Motol · CZUniversity of London · GBUniversity of Pavia · IT

Funding

Medical Research Council MC_UU_12014/12Medical Research Council MC_UU_12014/3Wellcome Trust 204870/Z/16/ZWellcome Trust WT090323MA
6 · The paper itself

Abstract

The genomic characteristics of human cytomegalovirus (HCMV) strains sequenced directly from clinical pathology samples were investigated, focusing on variation, multiple-strain infection, recombination, and gene loss. A total of 207 datasets generated in this and previous studies using target enrichment and high-throughput sequencing were analyzed, in the process enabling the determination of genome sequences for 91 strains. Key findings were that (i) it is important to monitor the quality of sequencing libraries in investigating variation; (ii) many recombinant strains have been transmitted during HCMV evolution, and some have apparently survived for thousands of years without further recombination; (iii) mutants with nonfunctional genes (pseudogenes) have been circulating and recombining for long periods and can cause congenital infection and resulting clinical sequelae; and (iv) intrahost variation in single-strain infections is much less than that in multiple-strain infections. Future population-based studies are likely to continue illuminating the evolution, epidemiology, and pathogenesis of HCMV.

Indexed as

Base SequenceGenome, ViralRecombination, GeneticCytomegalovirusCytomegalovirus InfectionsDatabases, Nucleic AcidDatasets as TopicDNA, ViralEvolution, MolecularGenes, ViralGenetic VariationGenotypeHigh-Throughput Nucleotide SequencingHumansMutationSequence Analysis, DNADNA, Viralgene lossgenome sequencegenotypehuman cytomegalovirusmultiple-strain infectionmutationrecombinationtarget enrichmentvariation

Identifiers

PMID31050742
PMCPMC6667795
OpenAlexW2950963668

What OpenQuestion holds

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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.