Evidence map›Paper›PMID 18281399›Full record

ArticleJournal of bacteriology2008

Late-stage polyribitol phosphate wall teichoic acid biosynthesis in Staphylococcus aureus.

Timothy C Meredith, Jonathan G Swoboda, Suzanne Walker

Open access · greenAbstract read
In one paragraph

Article in Journal of bacteriology, 2008. 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
2.9field-weighted citation impact, top 9% 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

58 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Role of staphylococcal EzrA as a molecular organizer of cell division.bioRxiv : the preprint server for biology · 2026
    Article
  5. 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
  6. Article
  7. Cryo-EM analysis ofScience advances · 2024
    Article
  8. Genome-wide transcription response ofFrontiers in microbiology · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Disruption of theJournal of bacteriology · 2022
    Article
  14. Targeting the Achilles' Heel of Multidrug-ResistantInternational journal of molecular sciences · 2022
    Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Lipoteichoic acid polymer length is determined by competition between free starter units.Proceedings of the National Academy of Sciences of the United States of America · 2020
    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

3 authors at 1 institution in 1 country.

Timothy C MeredithDepartment of Microbiology and Molecular Genetics, Harvard Medical School, 200 Longwood Ave., Boston, MA 02115, USA.
Jonathan G Swoboda
Suzanne Walker
Harvard University · US

Funding

INFECTIOUS DISEASE AND BASIC MICROBIOLOGICAL MECHANISMST32AI007061 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Marcia B Goldberg · 1985 to 2026
$12.1M
Wall Teichoic Acid Biosynthesis: A New Target for Therapeutic Intervention?R01GM078477 · NIGMS · HARVARD MEDICAL SCHOOL · PI WALKER, SUZANNE · 2007 to 2010
$1.7M
NIAID NIH HHS T32 AI007061NIAID NIH HHS T32-AI07061-30NIGMS NIH HHS GM078477NIGMS NIH HHS R01 GM078477PHS HHS F3178727
6 · The paper itself

Abstract

Wall teichoic acids are cell wall polymers that maintain the integrity of the cellular envelope and contribute to the virulence of Staphylococcus aureus. Despite the central role of wall teichoic acid in S. aureus virulence, details concerning the biosynthetic pathway of the predominant wall teichoic acid polymer are lacking, and workers have relied on a presumed similarity to the putative polyribitol phosphate wall teichoic acid pathway in Bacillus subtilis. Using high-resolution polyacrylamide gel electrophoresis for analysis of wall teichoic acid extracted from gene deletion mutants, a revised assembly pathway for the late-stage ribitol phosphate-utilizing enzymes is proposed. Complementation studies show that a putative ribitol phosphate polymerase, TarL, catalyzes both the addition of the priming ribitol phosphate onto the linkage unit and the subsequent polymerization of the polyribitol chain. It is known that the putative ribitol primase, TarK, is also a bifunctional enzyme that catalyzes both ribitol phosphate priming and polymerization. TarK directs the synthesis of a second, electrophoretically distinct polyribitol-containing teichoic acid that we designate K-WTA. The biosynthesis of K-WTA in S. aureus strain NCTC8325 is repressed by the accessory gene regulator (agr) system. The demonstration of regulated wall teichoic acid biosynthesis has implications for cell envelope remodeling in relation to S. aureus adhesion and pathogenesis.

Indexed as

Biosynthetic PathwaysBacterial ProteinsCell WallElectrophoresis, Polyacrylamide GelGene DeletionGene OrderGenes, BacterialGenetic Complementation TestPolysaccharidesStaphylococcus aureusStaphylococcus PhagesTeichoic AcidsTrans-ActivatorsTransferases (Other Substituted Phosphate Groups)Virus AttachmentAgr protein, Staphylococcus aureusBacterial ProteinsCDPribitol ribitolphosphotransferasepolyribitol phosphatePolysaccharidesTeichoic AcidsTrans-ActivatorsTransferases (Other Substituted Phosphate Groups)

Identifiers

PMID18281399
PMCPMC2293236
OpenAlexW2146538153

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.