Evidence map›Paper›PMID 34668723›Full record

ArticleMicrobiology spectrum2021

The Role of β-Glycosylated Wall Teichoic Acids in the Reduction of Vancomycin Susceptibility in Vancomycin-Intermediate Staphylococcus aureus.

Michael Hort, Ute Bertsche, Senada Nozinovic, Alina Dietrich, Anne Sophie Schrötter, Laura Mildenberger, Katharina Axtmann, Anne Berscheid, Gabriele Bierbaum

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  7. International journal of molecular sciences · 2024
    Article
  8. Molecular Aspects of the Functioning of Pathogenic Bacteria Biofilm Based onInternational journal of molecular sciences · 2024
    Review
  9. Lugdunin production and activity inMicrobiology spectrum · 2023
    Article
  10. Review
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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

9 authors at 3 institutions in 1 country.

Michael HortInstitute of Medical Microbiology, Immunology and Parasitology, University Clinics of Bonn, Bonn, Germany.
Ute BertscheDepartment of Infection Biology, University of Tuebingen, Tuebingen, Germany.
Senada NozinovicDepartment of Chemistry, University of Bonngrid.10388.32, Bonn, Germany.
Alina DietrichInstitute of Medical Microbiology, Immunology and Parasitology, University Clinics of Bonn, Bonn, Germany.
Anne Sophie SchrötterInstitute of Medical Microbiology, Immunology and Parasitology, University Clinics of Bonn, Bonn, Germany.
Laura MildenbergerInstitute of Medical Microbiology, Immunology and Parasitology, University Clinics of Bonn, Bonn, Germany.
Katharina AxtmannInstitute of Medical Microbiology, Immunology and Parasitology, University Clinics of Bonn, Bonn, Germany.
Anne BerscheidInstitute of Medical Microbiology, Immunology and Parasitology, University Clinics of Bonn, Bonn, Germany.ORCID 0000-0003-1585-8715
Gabriele BierbaumInstitute of Medical Microbiology, Immunology and Parasitology, University Clinics of Bonn, Bonn, Germany.ORCID 0000-0002-2933-8473
University Hospital Bonn · DEUniversity of Bonn · DEUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Staphylococcus aureus is an opportunistic pathogen that causes a wide range of infections. Due to the rapid evolution of antibiotic resistance that leads to treatment failure, it is important to understand the underlying mechanisms. Here, the cell wall structures of several laboratory vancomycin-intermediate S. aureus (VISA) strains were analyzed. Among the VISA strains were S. aureus VC40, which accumulated 79 mutations, including most importantly 2 exchanges in the histidine-kinase VraS, and developed full resistance against vancomycin (MIC, 64 μg/ml); a revertant S. aureus VC40R, which has an additional mutation in

Indexed as

Anti-Bacterial AgentsBacterial ProteinsCell WallDNA-Binding ProteinsGlycosylationMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsMutationPeptidoglycanStaphylococcal InfectionsStaphylococcus aureusTeichoic AcidsVancomycinVancomycin-Resistant Staphylococcus aureusAnti-Bacterial AgentsBacterial ProteinsDNA-Binding ProteinsPeptidoglycanTeichoic AcidsVancomycinVraR protein, Staphylococcus aureusVraS protein, Staphylococcus aureusautolysispeptidoglycantarStwo-component systemsvancomycin-intermediate S. aureusvraSRwall teichoic acids

Identifiers

PMID34668723
PMCPMC8528128
OpenAlexW3205265883

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.