Evidence map›Paper›PMID 27206613›Full record

ArticleBMC microbiology2016

Association between genotypic diversity and biofilm production in group B Streptococcus.

Robert E Parker, Clare Laut, Jennifer A Gaddy, Ruth N Zadoks, H Dele Davies, Shannon D Manning

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

38 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Article
  3. Comparison of cytokine responses to group BInfection and immunity · 2025
    Article
  4. Article
  5. Genomic adaptation in group BbioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. Emergence of High-Level Gentamicin Resistance inAntibiotics (Basel, Switzerland) · 2024
    Article
  9. Review
  10. Characteristics of Streptococcus agalactiae belonging to CC103 clone circulating among dairy herds and pregnant women in Brazil.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Group BACS infectious diseases · 2021
    Article
  18. Article
  19. Article
  20. Article
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

6 authors at 4 institutions in 2 countries.

Robert E ParkerDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI, USA.
Clare LautDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI, USA.
Jennifer A GaddyTennessee Valley Healthcare System, Department of Veterans Affairs, Nashville, TN, USA.
Ruth N ZadoksInstitute for Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, UK.
H Dele DaviesUniversity of Nebraska Medical School, Omaha, NE, USA.
Shannon D ManningDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI, USA. mannin71@msu.edu.
Michigan State University · USUniversity of Glasgow · GBUniversity of Nebraska Medical Center · USVanderbilt University · US

Funding

Regulation of Helicobacter pylori pili encoded by the cag pathogenicity islandIK2BX001701 · VA · VETERANS HEALTH ADMINISTRATION · PI GADDY, JENNIFER A · 2013 to 2017
–
6 · The paper itself

Abstract

backgroundGroup B Streptococcus (GBS) is a leading cause of sepsis and meningitis and an important factor in premature and stillbirths. Biofilm production has been suggested to be important for GBS pathogenesis alongside many other elements, including phylogenetic lineage and virulence factors, such as pili and capsule type. A complete understanding of the confluence of these components, however, is lacking. To identify associations between biofilm phenotype, pilus profile and lineage, 293 strains from asymptomatic carriers, invasive disease cases, and bovine mastitis cases, were assessed for biofilm production using an in vitro assay.

resultsMultilocus sequence type (ST) profile, pilus island profile, and isolate source were associated with biofilm production. Strains from invasive disease cases and/or belonging to the ST-17 and ST-19 lineages were significantly more likely to form weak biofilms, whereas strains producing strong biofilms were recovered more frequently from individuals with asymptomatic colonization.

conclusionsThese data suggest that biofilm production is a lineage-specific trait in GBS and may promote colonization of strains representing lineages other than STs 17 and 19. The findings herein also demonstrate that biofilms must be considered in the treatment of pregnant women, particularly for women with heavy GBS colonization.

Indexed as

BiofilmsAnimalsBacterial ProteinsCattleFimbriae, BacterialGenetic VariationGenotypeHumansMultilocus Sequence TypingPhylogenyStreptococcus agalactiaeVirulence FactorsBacterial ProteinsVirulence Factors

Identifiers

PMID27206613
PMCPMC4875601
OpenAlexW2396920338

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.