Evidence map›Paper›PMID 33382036›Full record

ArticleeLife2020

Mixed cytomegalovirus genotypes in HIV-positive mothers show compartmentalization and distinct patterns of transmission to infants.

Juanita Pang, Jennifer A Slyker, Sunando Roy, Josephine Bryant, Claire Atkinson, Juliana Cudini, Carey Farquhar, Paul Griffiths, James Kiarie, Sofia Morfopoulou and 6 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Observational
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  7. Genomic and geographical structure of human cytomegalovirus.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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 4 institutions in 4 countries.

Juanita Pang *Division of Infection and Immunity, University College London, Cruciform Building, London, United Kingdom.ORCID 0000-0002-4792-5903
Jennifer A Slyker *Departments of Global Health and Epidemiology, University of Washington, Seattle, United States.
Sunando RoyDivision of Infection and Immunity, University College London, Cruciform Building, London, United Kingdom.
Josephine BryantDivision of Infection and Immunity, University College London, Cruciform Building, London, United Kingdom.
Claire AtkinsonInstitute of Immunology and Transplantation, Division of Infection and Immunity, University College London, London, United Kingdom.
Juliana CudiniDivision of Infection and Immunity, University College London, Cruciform Building, London, United Kingdom.
Carey FarquharDepartments of Global Health, Epidemiology, Medicine (Div. Allergy and Infectious Diseases), University of Washington, Seattle, United States.
Paul GriffithsInstitute of Immunology and Transplantation, Division of Infection and Immunity, University College London, London, United Kingdom.
James KiarieUniversity of Nairobi, Department of Obstetrics and Gynaecology, World Health Organization, Nairobi, Kenya.
Sofia MorfopoulouDivision of Infection and Immunity, University College London, Cruciform Building, London, United Kingdom.
Alison C RoxbyDepartments of Global Health, Epidemiology, Medicine (Div. Allergy and Infectious Diseases), University of Washington, Seattle, United States.
Helena TutilDivision of Infection and Immunity, University College London, Cruciform Building, London, United Kingdom.
Rachel WilliamsDivision of Infection and Immunity, University College London, Cruciform Building, London, United Kingdom.
Soren GanttResearch Centre of the Sainte-Justine University Hospital, Department of Microbiology, Infectious Diseases and Immunology, University of Montréal QC, Montréal, Canada.ORCID 0000-0001-5743-3606
Richard A Goldstein *Division of Infection and Immunity, University College London, Cruciform Building, London, United Kingdom.ORCID 0000-0001-5148-4672
Judith Breuer *Department of Infection, Immunity and Inflammation, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.ORCID 0000-0001-8246-0534
University College London · GBUniversity of Washington · USCentre Hospitalier Universitaire Sainte-Justine · CAUniversity of Nairobi · KE

Funding

University of Washington/Fred Hutch Center for AIDS ResearchP30AI027757 · NIAID · UNIVERSITY OF WASHINGTON · PI CONNIE L CELUM · 1988 to 2026
$104.9M
VENEREAL DISEASET32AI007140 · NIAID · UNIVERSITY OF WASHINGTON · PI Julia Cook Dombrowski · 1985 to 2026
$19.4M
THE ROLE OF ANTIBODIES IN MOTHER TO CHILD HIV TRANSMISSIONR01AI076105 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI OVERBAUGH, JULIE M. · 2008 to 2023
$8.8M
Pediatric HIV-1 in Africa: Pathogenesis and ManagementK24HD054314 · NICHD · UNIVERSITY OF WASHINGTON · PI JOHN-STEWART, GRACE C. · 2006 to 2016
$1.2M
Immune activation during pregnancy and contraception in HIV-infected Kenyan womenK23HD071788 · NICHD · UNIVERSITY OF WASHINGTON · PI ROXBY, ALISON CHRISTINA · 2012 to 2016
$648k
HIV-1 and Protective Immunity against Common Childhood PathogensK24AI087399 · NIAID · UNIVERSITY OF WASHINGTON · PI FARQUHAR, CAREY · 2010 to 2014
$647k
Vertical CMV transmission in the setting of maternal HIV-1 infection in KenyaK01AI087369 · NIAID · UNIVERSITY OF WASHINGTON · PI SLYKER, JENNIFER ANN · 2010 to 2014
$616k
HSV-2 suppression to reduce maternal plasma, genital and breast milk HIV-1 levelsR03HD057773 · NICHD · UNIVERSITY OF WASHINGTON · PI FARQUHAR, CAREY · 2008 to 2009
$203k
Biotechnology and Biological Sciences Research Council BB/P007562/1NIAID NIH HHS K01 AI087369NIAID NIH HHS K24 AI087399NIAID NIH HHS P30 AI027757NIAID NIH HHS R01 AI076105NIAID NIH HHS T32 AI007140NICHD NIH HHS K23 HD071788NICHD NIH HHS K24 HD054314NICHD NIH HHS R03 HD057773Wellcome Trust 204870Wellcome Trust 204870/Z/16/ZWellcome Trust 206478Wellcome Trust 206478/Z/17/ZWorld Health Organization 001
6 · The paper itself

Abstract

Cytomegalovirus (CMV) is the commonest cause of congenital infection and particularly so among infants born to HIV-infected women. Studies of congenital CMV infection (cCMVi) pathogenesis are complicated by the presence of multiple infecting maternal CMV strains, especially in HIV-positive women, and the large, recombinant CMV genome. Using newly developed tools to reconstruct CMV haplotypes, we demonstrate anatomic CMV compartmentalization in five HIV-infected mothers and identify the possibility of congenitally transmitted genotypes in three of their infants. A single CMV strain was transmitted in each congenitally infected case, and all were closely related to those that predominate in the cognate maternal cervix. Compared to non-transmitted strains, these congenitally transmitted CMV strains showed statistically significant similarities in 19 genes associated with tissue tropism and immunomodulation. In all infants, incident superinfections with distinct strains from breast milk were captured during follow-up. The results represent potentially important new insights into the virologic determinants of early CMV infection.

Indexed as

Infectious Disease Transmission, VerticalCytomegalovirusCytomegalovirus InfectionsFemaleGenotypeHIV InfectionsHumansInfant, NewbornMothersPregnancycongenitalcytomegalovirusgeneticsgenomegenomicsinfectious diseasemicrobiologysequencingtransmissionvirus

Identifiers

PMID33382036
PMCPMC7806273
OpenAlexW3115653116

What Socratic 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 Socratic graph.