Evidence map›Paper›PMID 27791478›Full record

ArticleVirulence2017

Differing mechanisms of surviving phagosomal stress among group B Streptococcus strains of varying genotypes.

Michelle L Korir, Clare Laut, Lisa M Rogers, Jessica A Plemmons, David M Aronoff, Shannon D Manning

Open access · goldAbstract read
In one paragraph

Article in Virulence, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.9field-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

31 citing papers in PubMed, 39 citations in OpenAlex.

  1. CorAVeterinary research · 2026
    Article
  2. Article
  3. Genomic adaptation in group BbioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Specific interaction between Group BInfection and immunity · 2024
    Article
  8. Article
  9. Article
  10. Macrophage polarization duringFrontiers in microbiology · 2023
    Article
  11. Article
  12. ACS infectious diseases · 2022
    Article
  13. Article
  14. Article
  15. Nitric Oxide InducedMicroorganisms · 2022
    Article
  16. Article
  17. Distinct Group BInfection and immunity · 2021
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Michelle L Korira Department of Microbiology and Molecular Genetics , Michigan State University , East Lansing , MI , USA.
Clare Lauta Department of Microbiology and Molecular Genetics , Michigan State University , East Lansing , MI , USA.
Lisa M Rogersb Department of Medicine , Vanderbilt University , Nashville , TN , USA.
Jessica A Plemmonsa Department of Microbiology and Molecular Genetics , Michigan State University , East Lansing , MI , USA.
David M Aronoffb Department of Medicine , Vanderbilt University , Nashville , TN , USA.ORCID 0000-0003-4587-6121
Shannon D Manninga Department of Microbiology and Molecular Genetics , Michigan State University , East Lansing , MI , USA.
Michigan State University · USVanderbilt University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Group B Streptococcus (GBS), a leading cause of neonatal sepsis and meningitis, asymptomatically colonizes up to 30% of women and can persistently colonize even after antibiotic treatment. Previous studies have shown that GBS resides inside macrophages, but the mechanism by which it survives remains unknown. Here, we examined the ability of 4 GBS strains to survive inside macrophages and then focused on 2 strains belonging to sequence type (ST)-17 and ST-12, to examine persistence in the presence of antibiotics. A multiple stress medium was also developed using several stressors found in the phagosome to assess the ability of 30 GBS strains to withstand phagosomal stress. The ST-17 strain was more readily phagocytosed and survived intracellularly longer than the ST-12 strain, but the ST-12 strain was tolerant to ampicillin unlike the ST-17 strain. Exposure to sub-inhibitory concentrations of ampicillin and erythromycin increased the level of phagocytosis of the ST-17 strain, but had no effect on the ST-12 strain. In addition, blocking acidification of the phagosome decreased the survival of the ST-17 strain indicating a pH-dependent survival mechanism for the ST-17 strain. Congruent with the macrophage experiments, the ST-17 strain had a higher survival rate in the multiple stress medium than the ST-12 strain, and overall, serotype III isolates survived significantly better than other serotypes. These results indicate that diverse GBS strains may use differing mechanisms to persist and that serotype III strains are better able to survive specific stressors inside the phagosome relative to other serotypes.

Indexed as

Stress, PhysiologicalAdultAnti-Bacterial AgentsGenotypeHumansMacrophagesPhagocytosisPhagosomesSerogroupSerotypingStreptococcal InfectionsStreptococcus agalactiaeTHP-1 CellsVirulence FactorsAnti-Bacterial AgentsVirulence FactorsGroup B Streptococcusintracellular survivalmacrophagesphagocytosisStreptococcus agalactiae

Identifiers

PMID27791478
PMCPMC5626345
OpenAlexW2542532036

What OpenQuestion holds

Textmetadata
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.