Evidence map›Paper›PMID 24603861›Full record

ArticlePLoS pathogens2014

Group B streptococcal infection of the choriodecidua induces dysfunction of the cytokeratin network in amniotic epithelium: a pathway to membrane weakening.

Jeroen P Vanderhoeven, Craig J Bierle, Raj P Kapur, Ryan M McAdams, Richard P Beyer, Theo K Bammler, Federico M Farin, Aasthaa Bansal, Min Spencer, Mei Deng and 4 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Re-framing the importance of Group BInfection and immunity · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Vertical Transmission of Group BInternational journal of microbiology · 2024
    Article
  9. Article
  10. Nitric Oxide Production and Effects in Group BPathogens (Basel, Switzerland) · 2022
    Article
  11. Mechanisms of group BReproduction & fertility · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Immunobiology of Acute Chorioamnionitis.Frontiers in immunology · 2020
    Review
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

14 authors at 3 institutions in 1 country.

Jeroen P VanderhoevenDepartment of Obstetrics & Gynecology, University of Washington, Seattle, Washington, United States of America.
Craig J BierleCenter for Childhood Infections and Prematurity Research, Seattle Children's Research Institute, Seattle, Washington, United States of America.
Raj P KapurDepartments of Pathology, Seattle Children's and University of Washington, Seattle, Washington, United States of America.
Ryan M McAdamsDepartment of Pediatrics, University of Washington, Seattle, Washington, United States of America.
Richard P BeyerDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington, United States of America.
Theo K BammlerDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington, United States of America.
Federico M FarinDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington, United States of America.
Aasthaa BansalDepartment of Biostatistics, University of Washington, Seattle, Washington, United States of America.
Min SpencerCenter on Human Development and Disability, University of Washington, Seattle, Washington, United States of America.
Mei DengCenter on Human Development and Disability, University of Washington, Seattle, Washington, United States of America.
Michael G GravettDepartment of Obstetrics & Gynecology, University of Washington, Seattle, Washington, United States of America; Global Alliance to Prevent Prematurity & Stillbirth, Seattle, Washington, United States of America.
Craig E RubensCenter for Childhood Infections and Prematurity Research, Seattle Children's Research Institute, Seattle, Washington, United States of America; Department of Pediatrics, University of Washington, Seattle, Washington, United States of America; Global Alliance to Prevent Prematurity & Stillbirth, Seattle, Washington, United States of America.
Lakshmi RajagopalCenter for Childhood Infections and Prematurity Research, Seattle Children's Research Institute, Seattle, Washington, United States of America; Department of Pediatrics, University of Washington, Seattle, Washington, United States of America.
Kristina M Adams WaldorfDepartment of Obstetrics & Gynecology, University of Washington, Seattle, Washington, United States of America; Center on Human Development and Disability, University of Washington, Seattle, Washington, United States of America.
University of Washington · USGlobal Alliance to Prevent Prematurity and Stillbirth · USSeattle Children's Hospital · US

Funding

Washington National Primate Research CenterP51OD010425 · OD · UNIVERSITY OF WASHINGTON · PI Mari Ostendorf · 2012 to 2026
$201.8M
INSTITUTE FOR TRANSLATIONAL HEALTH SCIENCE (UL1): BPCAUL1RR025014 · NCRR · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2007 to 2011
$51.5M
Institute of Translational Health SciencesUL1TR000423 · NCATS · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2012 to 2016
$49.4M
Restoring FMRP Phenotypes Frpm Temporal Regional and Splice- Isoforms VarationsP30HD002274 · NICHD · UNIVERSITY OF WASHINGTON · PI GURALNICK, MICHAEL J · 1985 to 2013
$33.6M
WOMEN'S REPRODUCTIVE HEALTH RESEARCH CAREER DEVELOPMENTK12HD001264 · NICHD · UNIVERSITY OF WASHINGTON · PI Barbara Ann Goff · 1998 to 2026
$8.6M
Intellectual and Developmental Disabilities Research CenterU54HD083091 · NICHD · UNIVERSITY OF WASHINGTON · PI DOHERTY, DANIEL · 2014 to 2019
$7.9M
GBS mediated in utero fetal injuryR01AI100989 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI ADAMS WALDORF, KRISTINA M., RAJAGOPAL, LAKSHMI · 2012 to 2016
$3.9M
Toll-Like Receptor Antagonism as a Potential Treatment for Preterm LaborK08AI067910 · NIAID · UNIVERSITY OF WASHINGTON · PI ADAMS WALDORF, KRISTINA M. · 2007 to 2011
$632k
NCATS NIH HHS UL1 TR000423NCRR NIH HHS UL1 RR025014NCRR NIH HHS UL1RR025014NIAID NIH HHS K08 AI067910NIAID NIH HHS K08AI067910NIAID NIH HHS R01 AI100989NIAID NIH HHS R01AI100989NICHD NIH HHS K12 HD001264NICHD NIH HHS K12HD001264NICHD NIH HHS P30 HD002274NICHD NIH HHS P30HD002274NICHD NIH HHS U54 HD083091NIH HHS P51 OD010425
6 · The paper itself

Abstract

Early events leading to intrauterine infection remain poorly defined, but may hold the key to preventing preterm delivery. To determine molecular pathways within fetal membranes (chorioamnion) associated with early choriodecidual infection that may progress to preterm premature rupture of membranes (PPROM), we examined the effects of a Group B Streptococcus (GBS) choriodecidual infection on chorioamnion in a nonhuman primate model. Ten chronically catheterized pregnant monkeys (Macaca nemestrina) at 118-125 days gestation (term = 172 days) received choriodecidual inoculation of either GBS (n = 5) or saline (n = 5). Cesarean section was performed in the first week after GBS or saline inoculation. RNA extracted from chorioamnion (inoculation site) was profiled by microarray. Single gene, Gene Set, and Ingenuity Pathway Analysis results were validated using qRT-PCR (chorioamnion), Luminex (amniotic fluid, AF), immunohistochemistry, and transmission electron microscopy (TEM). Despite uterine quiescence in most cases, significant elevations of AF cytokines (TNF-α, IL-8, IL-1β, IL-6) were detected in GBS versus controls (p<0.05). Choriodecidual infection resolved by the time of cesarean section in 3 of 5 cases and GBS was undetectable by culture and PCR in the AF. A total of 331 genes were differentially expressed (>2-fold change, p<0.05). Remarkably, GBS exposure was associated with significantly downregulated expression of multiple cytokeratin (CK) and other cytoskeletal genes critical for maintenance of tissue tensile strength. Immunofluorescence revealed highly significant changes in the CK network within amniocytes with dense CK aggregates and retraction from the cell periphery (all p = 0.006). In human pregnancies affected by PPROM, there was further evidence of CK network retraction with significantly shorter amniocyte foot processes (p = 0.002). These results suggest early choriodecidual infection results in decreased cellular membrane integrity and tensile strength via dysfunction of CK networks. Downregulation of CK expression and perturbations in the amniotic epithelial cell intermediate filament network occur after GBS choriodecidual infection, which may contribute to PPROM.

Indexed as

AmnionAnimalsChorionDisease Models, AnimalFemaleFluorescent Antibody TechniqueHumansImmunohistochemistryKeratinsMacaca nemestrinaMicroscopy, ConfocalMicroscopy, Electron, TransmissionOligonucleotide Array Sequence AnalysisPregnancyPremature Rupture of Fetal MembranesPrenatal Exposure Delayed EffectsKeratins

Identifiers

PMID24603861
PMCPMC3946355
OpenAlexW2019654229

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.