Evidence map›Paper›PMID 24943359›Full record

ArticleBMC microbiology2014

Pilus distribution among lineages of group b streptococcus: an evolutionary and clinical perspective.

Amber Cody Springman, David W Lacher, Emily A Waymire, Samantha L Wengert, Pallavi Singh, Ruth N Zadoks, H Dele Davies, Shannon D Manning

Abstract read
In one paragraph

Article in BMC microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
–field-weighted citation impact
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

58 citing papers in PubMed.

  1. Article
  2. Article
  3. Towards a holistic epidemiology ofFrontiers in bioinformatics · 2026
    Article
  4. Article
  5. Article
  6. Zoonotic Approach toInternational journal of microbiology · 2026
    Article
  7. Review
  8. Article
  9. Genomic Diversity, Virulome, and Resistome ofPathogens (Basel, Switzerland) · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Molecular epidemiology and antibiotic resistance of group BFrontiers in cellular and infection microbiology · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Emergence of High-Level Gentamicin Resistance inAntibiotics (Basel, Switzerland) · 2024
    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

8 authors.

Amber Cody Springman
David W Lacher
Emily A Waymire
Samantha L Wengert
Pallavi Singh
Ruth N Zadoks
H Dele Davies
Shannon D ManningDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA. mannin71@msu.edu.

Funding

Genetic Diversity and Molecular Epidemiology of GBSR01AI066081 · NIAID · MICHIGAN STATE UNIVERSITY · PI DAVIES, HERBERT D · 2005 to 2008
$1.1M
NIAID NIH HHS AI066081
6 · The paper itself

Abstract

backgroundGroup B Streptococcus (GBS) is an opportunistic pathogen in both humans and bovines. Epidemiological and phylogenetic analyses have found strains belonging to certain phylogenetic lineages to be more frequently associated with invasive newborn disease, asymptomatic maternal colonization, and subclinical bovine mastitis. Pilus structures in GBS facilitate colonization and invasion of host tissues and play a role in biofilm formation, though few large-scale studies have estimated the frequency and diversity of the three pilus islands (PIs) across diverse genotypes. Here, we examined the distribution of pilus islands (PI) 1, 2a and 2b among 295 GBS strains representing 73 multilocus sequence types (STs) belonging to eight clonal complexes. PCR-based RFLP was also used to evaluate variation in the genes encoding pilus backbone proteins of PI-2a and PI-2b.

resultsAll 295 strains harbored one of the PI-2 variants and most human-derived strains contained PI-1. Bovine-derived strains lacked PI-1 and possessed a unique PI-2b backbone protein allele. Neonatal strains more frequently had PI-1 and a PI-2 variant than maternal colonizing strains, and most CC-17 strains had PI-1 and PI-2b with a distinct backbone protein allele. Furthermore, we present evidence for the frequent gain and loss of genes encoding certain pilus types.

conclusionsThese data suggest that pilus combinations impact host specificity and disease presentation and that diversification often involves the loss or acquisition of PIs. Such findings have implications for the development of GBS vaccines that target the three pilus islands.

Indexed as

Genes, BacterialGenomic IslandsAnimalsCattleCattle DiseasesDNA, BacterialFemaleFimbriae, BacterialGenotypeHost SpecificityHumansInfantInfant, NewbornMothersPolymerase Chain ReactionPolymorphism, Restriction Fragment LengthDNA, Bacterial

Identifiers

PMID24943359
PMCPMC4074840

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Registered trials

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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.