Evidence map›Paper›PMID 31779587›Full record

ArticleBMC infectious diseases2019

High prevalence of group B streptococcus ST17 hypervirulent clone among non-pregnant patients from a Hungarian venereology clinic.

Szilvia Kardos, Adrienn Tóthpál, Krisztina Laub, Katalin Kristóf, Eszter Ostorházi, Ferenc Rozgonyi, Orsolya Dobay

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Mechanisms and Manifestations of Group B Streptococcus Meningitis in Newborns.Journal of the Pediatric Infectious Diseases Society · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Molecular Identification of Invasive Non-typeable Group BFrontiers in cellular and infection microbiology · 2021
    Article
  10. Rapid Classification of Multilocus Sequence Subtype for Group BFrontiers in cellular and infection microbiology · 2020
    Article
  11. 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

7 authors at 1 institution in 1 country.

Szilvia KardosInstitute of Medical Microbiology, Semmelweis University, Nagyvárad tér 4, Budapest, H-1089, Hungary.
Adrienn TóthpálInstitute of Medical Microbiology, Semmelweis University, Nagyvárad tér 4, Budapest, H-1089, Hungary.
Krisztina LaubInstitute of Medical Microbiology, Semmelweis University, Nagyvárad tér 4, Budapest, H-1089, Hungary.
Katalin KristófInstitute of Laboratory Medicine, Semmelweis University, Budapest, Hungary.
Eszter OstorháziInstitute of Medical Microbiology, Semmelweis University, Nagyvárad tér 4, Budapest, H-1089, Hungary.
Ferenc RozgonyiInstitute of Laboratory Medicine, Semmelweis University, Budapest, Hungary.
Orsolya DobayInstitute of Medical Microbiology, Semmelweis University, Nagyvárad tér 4, Budapest, H-1089, Hungary. dobay.orsolya@med.semmelweis-univ.hu.ORCID http://orcid.org/0000-0001-7094-2288
Semmelweis University · HU

Funding

National Research, Development and Innovation Office / Hungarian Scientific Research Fund K108631Wellcome Trust
6 · The paper itself

Abstract

backgroundAlthough Streptococcus agalactiae is the leading causative agent of neonatal sepsis and meningitis, recently it is increasingly isolated from non-pregnant adults. The relation between its presence in the genitourinary tract and manifested clinical symptoms of STD patients remains an open question. In this study, a complex epidemiological investigation of GBS isolates from a venerology clinic was performed.

methodsNinety-six GBS isolates were serotyped and their genetic relatedness determined by PFGE. MLST was also performed for a subset of 20 isolates. The antibiotic susceptibility was tested with agar dilution. Surface proteins and the ST-17 hypervirulent clone was detected by PCR.

resultsThe serotype prevalence was the following: V (29.2%), III (27.1%), Ia (22.9%), IV (10.4%), II (5.2%) and Ib (4.2%). A strong association was demonstrated between surface protein genes and serotypes. All isolates were fully susceptible to penicillin, but erythromycin and clindamycin resistance was high (41.7 and 35.4%, respectively), and 8 phenotypically macrolide sensitive isolates carried the ermB gene. 21.9% of all strains belonged to the hypervirulent ST17 clone, most being of serotype III and all were rib +. We found a few serotype IV isolates belonging to several STs and one serotype V/ST110 strain, containing a 44-bp deletion in the atr allele.

conclusionsThe presence of silent ermB genes is of worry, as their expression upon macrolide exposure could lead to unforeseen therapeutic failure, while clindamycin is used for intrapartum antibiotic prophylaxis, in case of penicillin allergy. The other alarming result is the high prevalence of ST17 among these strains from STD patients, who could be sources of further infections. This is the first report from Hungary providing both serotyping and genotyping data of GBS isolates. These results could be helpful for vaccine production as the major vaccine candidates are capsular antigens or surface proteins.

Indexed as

AdultAnti-Bacterial AgentsBacterial ProteinsDNA, BacterialDrug Resistance, BacterialFemaleHumansHungaryMacrolidesMicrobial Sensitivity TestsPhenotypePrevalenceSerogroupStreptococcal InfectionsStreptococcus agalactiaeVirulenceAnti-Bacterial AgentsBacterial ProteinsDNA, BacterialMacrolidesGBSHypervirulent ST-17 cloneMacrolide resistanceSerotypesSurface proteins

Identifiers

PMID31779587
PMCPMC6883650
OpenAlexW2991425861

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.