Evidence map›Paper›PMID 25385795›Full record

ArticleInfection and immunity2015

Prolonged growth of a clinical Staphylococcus aureus strain selects for a stable small-colony-variant cell type.

Long M G Bui, Peter Hoffmann, John D Turnidge, Peter S Zilm, Stephen P Kidd

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

27 citing papers in PubMed, 52 citations in OpenAlex.

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  10. Review on skeletal disorders caused byThe veterinary quarterly · 2022
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  11. FunctionalJournal of bacteriology · 2022
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  13. The road to success of coagulase-negative staphylococci: clinical significance of small colony variants and their pathogenic role in persistent infections.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2021
    Review
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  15. Adaptation ofToxins · 2021
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  16. A Human Osteocyte Cell Line Model for StudyingFrontiers in cellular and infection microbiology · 2021
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  17. Novel Research Models forFrontiers in microbiology · 2020
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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

5 authors at 2 institutions in 1 country.

Long M G BuiResearch Centre for Infectious Disease, School of Molecular and Biomedical Science, The University of Adelaide, Adelaide, Australia.
Peter HoffmannAdelaide Proteomics Centre, School of Molecular and Biomedical Science, The University of Adelaide, Adelaide, Australia.
John D TurnidgeSA Pathology, Women's and Children's Hospital, Adelaide, Australia.
Peter S ZilmOral Microbiology Laboratory, School of Dentistry, The University of Adelaide, Adelaide, Australia.
Stephen P KiddResearch Centre for Infectious Disease, School of Molecular and Biomedical Science, The University of Adelaide, Adelaide, Australia stephen.kidd@adelaide.edu.au.
University of Adelaide · AUWomen's and Children's Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An undetermined feature of Staphylococcus aureus pathogenesis is its persistence and then relapse of disease. This has been explained by its switch to alternative lifestyles, mainly as biofilm or small-colony variants (SCVs). Studying the native characteristics of SCVs has been problematic due to their reversion to the parental lifestyle. We have observed that for a number of S. aureus strains as they switch to an SCV lifestyle, there is the formation of an extracellular matrix. We focused our analysis on one strain, WCH-SK2. For bacterial survival in the host, the combination of low nutrients and the prolonged time frame forms a stress that selects for a specific cell type from the population. In this context, we used steady-state growth conditions with low nutrients and a controlled low growth rate for a prolonged time and with methylglyoxal. These conditions induced S. aureus WCH-SK2 into a stable SCV cell type; the cells did not revert after subculturing. Analysis revealed these cells possessed a metabolic and surface profile that was different from those of previously described SCVs or biofilm cells. The extracellular matrix was protein and extracellular DNA but not polysaccharide. The SCV cells induced expression of certain surface proteins (such as Ebh) and synthesis of lantibiotics while downregulating factors that stimulate the immune response (leucocidin, capsule, and carotenoid). Our data reveal cell heterogeneity within an S. aureus population and under conditions that resemble long-term survival in the host have identified a previously unnoticed S. aureus cell type with a distinctive metabolic and molecular profile.

Indexed as

Adaptation, PhysiologicalAnti-Bacterial AgentsBiofilmsDrug Resistance, Multiple, BacterialExtracellular MatrixGene Expression Regulation, BacterialHumansMicrobial Sensitivity TestsPyruvaldehydeStaphylococcal InfectionsStaphylococcus aureusAnti-Bacterial AgentsPyruvaldehyde

Identifiers

PMID25385795
PMCPMC4294242
OpenAlexW2127269879

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.