Evidence map›Paper›PMID 20463161›Full record

ArticleJournal of clinical microbiology2010

Phylogenetic analysis of rubella viruses involved in congenital rubella infections in France between 1995 and 2009.

Christelle Vauloup-Fellous, Judith M Hübschen, Emily S Abernathy, Joseph Icenogle, Nicolas Gaidot, Pascal Dubreuil, Isabelle Parent-du-Châtelet, Liliane Grangeot-Keros, Claude P Muller

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In one paragraph

Article in Journal of clinical microbiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Viral invasion of the amniotic cavity (VIAC) in the midtrimester of pregnancy.The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians · 2012
    Article
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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

9 authors at 6 institutions in 3 countries.

Christelle Vauloup-FellousINSERM U764, Université Paris-Sud, AP-HP, Microbiology Department, Hôpital Antoine Béclère, Clamart, France. christelle.vauloup@abc.aphp.fr
Judith M Hübschen
Emily S Abernathy
Joseph Icenogle
Nicolas Gaidot
Pascal Dubreuil
Isabelle Parent-du-Châtelet
Liliane Grangeot-Keros
Claude P Muller
Assistance Publique – Hôpitaux de Paris · FRCenters for Disease Control and Prevention · USLaboratoire National de Santé · LUHôpital Antoine-Béclère · FRInstitut de Veille Sanitaire · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rubella is an acute infectious disease that normally has a mild clinical course. However, infections during pregnancy, especially before week 12 of gestation (WG), can cause severe birth defects known as congenital rubella syndrome (CRS). The aim of this study was to perform genotyping and molecular characterization of rubella viruses involved in congenital infections in France over the past 15 years (1995 to 2009). Amniotic fluid (AF) specimens (n = 80) from pregnant women with congenital rubella infections (CRI) before week 20 of gestation, and a few other samples available from children/newborns with CRS (n = 26), were analyzed. The coding region of the rubella virus E1 gene was amplified directly from clinical specimens by reverse transcriptase PCR, and the resulting DNA fragments were sequenced. Sequences were assigned to genotypes by phylogenetic analysis with rubella virus reference sequences. Sufficient E1 gene sequences were obtained from 56 cases. Phylogenetic analysis of the sequences showed that at least five different genotypes (1E, 1G, 1B, 2B, and 1h) were present in France and were involved in congenital infections, with a strong predominance of genotype 1E (87%). This is one of the very few comprehensive studies of rubella viruses involved in CRI. The results indicated that over the past 15 years, multiple introductions of the dominant genotype E caused most of the CRI cases in France. A few sporadic cases were due to other genotypes (1B, 1G, 1h, 2B).

Indexed as

Rubella Syndrome, CongenitalAmniotic FluidCluster AnalysisFemaleFranceHumansMolecular EpidemiologyPhylogenyPregnancyRNA, ViralRubella virusViral Envelope ProteinsE1 envelope protein, Rubella virusRNA, ViralViral Envelope Proteins

Identifiers

PMID20463161
PMCPMC2897492
OpenAlexW2167870890

What OpenQuestion holds

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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.