Evidence map›Paper›PMID 23027967›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Methicillin resistance in Staphylococcus aureus requires glycosylated wall teichoic acids.

Stephanie Brown, Guoqing Xia, Lyly G Luhachack, Jennifer Campbell, Timothy C Meredith, Calvin Chen, Volker Winstel, Cordula Gekeler, Javier E Irazoqui, Andreas Peschel and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 170 papers.

0numbers the graph read from it
0cells of the map it votes in
170citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

170 citing papers in PubMed, 294 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Science advances · 2026
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  6. Host-driven remodelling of theMicrobiology (Reading, England) · 2026
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  8. Mutation of lipoprotein processing pathway geneAntimicrobial agents and chemotherapy · 2026
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  11. Phage P100 resistance in clinical and foodborneCurrent research in microbial sciences · 2026
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  14. Mechanistic study on the susceptibility ofApplied and environmental microbiology · 2025
    Article
  15. Article
  16. SpbR controls lipoteichoic acid length by directly inhibiting signal peptidase SpsB inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Review
  18. Article
  19. Article
  20. Article

110 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Stephanie BrownDepartment of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA.
Guoqing Xia
Lyly G Luhachack
Jennifer Campbell
Timothy C Meredith
Calvin Chen
Volker Winstel
Cordula Gekeler
Javier E Irazoqui
Andreas Peschel
Suzanne Walker
Harvard University · USUniversity of Tübingen · DEMassachusetts General Hospital · US

Funding

Technical Mother Machine CoreP01AI083214 · NIAID · SCHEPENS EYE RESEARCH INSTITUTE · PI Michael S Gilmore · 2009 to 2026
$39.4M
Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
INFECTIOUS DISEASE AND BASIC MICROBIOLOGICAL MECHANISMST32AI007061 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Marcia B Goldberg · 1985 to 2026
$12.1M
Identifying and validating new antibiotic targets in cell wall synthesis pathwaysR01AI099144 · NIAID · HARVARD MEDICAL SCHOOL · PI BERNHARDT, THOMAS G, WALKER, SUZANNE · 2012 to 2016
$4.3M
Role of MiT Transcription Factors in Host Defense Against Bacterial InfectionR01GM101056 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI IRAZOQUI, JAVIER ELBIO · 2012 to 2022
$3.9M
NIAID NIH HHS 1R01AI099144NIAID NIH HHS P01 AI083214NIAID NIH HHS P01AI083214NIAID NIH HHS R01 AI099144NIAID NIH HHS T32 AI007061NIAID NIH HHS T32AI007061NIDDK NIH HHS P30 DK043351NIGMS NIH HHS R01 GM101056
6 · The paper itself

Abstract

Staphylococcus aureus peptidoglycan (PG) is densely functionalized with anionic polymers called wall teichoic acids (WTAs). These polymers contain three tailoring modifications: d-alanylation, α-O-GlcNAcylation, and β-O-GlcNAcylation. Here we describe the discovery and biochemical characterization of a unique glycosyltransferase, TarS, that attaches β-O-GlcNAc (β-O-N-acetyl-D-glucosamine) residues to S. aureus WTAs. We report that methicillin resistant S. aureus (MRSA) is sensitized to β-lactams upon tarS deletion. Unlike strains completely lacking WTAs, which are also sensitive to β-lactams, ΔtarS strains have no growth or cell division defects. Because neither α-O-GlcNAc nor β-O-Glucose modifications can confer resistance, the resistance phenotype requires a highly specific chemical modification of the WTA backbone, β-O-GlcNAc residues. These data suggest β-O-GlcNAcylated WTAs scaffold factors required for MRSA resistance. The β-O-GlcNAc transferase identified here, TarS, is a unique target for antimicrobials that sensitize MRSA to β-lactams.

Indexed as

AnimalsBacterial Proteinsbeta-LactamsCell WallGene DeletionGlycosylationGlycosyltransferasesHumansMethicillin ResistanceMethicillin-Resistant Staphylococcus aureusTeichoic AcidsBacterial Proteinsbeta-LactamsGlycosyltransferasesTeichoic Acids

Identifiers

PMID23027967
PMCPMC3503181
OpenAlexW2000478943

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.