Evidence map›Paper›PMID 23438756›Full record

ArticleChemistry & biology2013

Discovery of wall teichoic acid inhibitors as potential anti-MRSA β-lactam combination agents.

Hao Wang, Charles J Gill, Sang H Lee, Paul Mann, Paul Zuck, Timothy C Meredith, Nicholas Murgolo, Xinwei She, Susan Kales, Lianzhu Liang and 12 more

Abstract read
In one paragraph

Article in Chemistry & biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
–field-weighted citation impact
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

71 citing papers in PubMed.

  1. In Silico Lead Identification ofInternational journal of molecular sciences · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Unveiling the Multifaceted Capabilities of EndophyticPharmaceuticals (Basel, Switzerland) · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Targeting the Achilles' Heel of Multidrug-ResistantInternational journal of molecular sciences · 2022
    Article
  13. Review
  14. Review
  15. Structure-Based Discovery of Lipoteichoic Acid Synthase Inhibitors.Journal of chemical information and modeling · 2022
    Article
  16. Article
  17. Review
  18. Review
  19. Rapid Inhibitor Discovery by Exploiting Synthetic Lethality.Journal of the American Chemical Society · 2022
    Article
  20. Review

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

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

22 authors.

Hao WangInfectious Disease Biology, Merck Research Laboratories, Kenilworth, NJ 07033, USA.
Charles J Gill
Sang H Lee
Paul Mann
Paul Zuck
Timothy C Meredith
Nicholas Murgolo
Xinwei She
Susan Kales
Lianzhu Liang
Jenny Liu
Jin Wu
John Santa Maria
Jing Su
Jianping Pan
Judy Hailey
Debra Mcguinness
Christopher M Tan
Amy Flattery
Suzanne Walker
Todd Black
Terry Roemer

Funding

Technical Mother Machine CoreP01AI083214 · NIAID · SCHEPENS EYE RESEARCH INSTITUTE · PI Michael S Gilmore · 2009 to 2026
$39.4M
INFECTIOUS DISEASE AND BASIC MICROBIOLOGICAL MECHANISMST32AI007061 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Marcia B Goldberg · 1985 to 2026
$12.1M
NIAID NIH HHS P01 AI083214NIAID NIH HHS T32 AI007061
6 · The paper itself

Abstract

Innovative strategies are needed to combat drug resistance associated with methicillin-resistant Staphylococcus aureus (MRSA). Here, we investigate the potential of wall teichoic acid (WTA) biosynthesis inhibitors as combination agents to restore β-lactam efficacy against MRSA. Performing a whole-cell pathway-based screen, we identified a series of WTA inhibitors (WTAIs) targeting the WTA transporter protein, TarG. Whole-genome sequencing of WTAI-resistant isolates across two methicillin-resistant Staphylococci spp. revealed TarG as their common target, as well as a broad assortment of drug-resistant bypass mutants mapping to earlier steps of WTA biosynthesis. Extensive in vitro microbiological analysis and animal infection studies provide strong genetic and pharmacological evidence of the potential effectiveness of WTAIs as anti-MRSA β-lactam combination agents. This work also highlights the emerging role of whole-genome sequencing in antibiotic mode-of-action and resistance studies.

Indexed as

Amino Acid SubstitutionAnti-Bacterial AgentsBacterial Proteinsbeta-LactamsCell WallDrug Evaluation, PreclinicalDrug Resistance, BacterialGenome, BacterialMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsOsmolar ConcentrationPhenotypeSequence Analysis, DNATeichoic AcidsTemperatureAnti-Bacterial AgentsBacterial Proteinsbeta-LactamsTeichoic Acids

Identifiers

PMID23438756
PMCPMC3762323

What OpenQuestion holds

Textmetadata
LicenceTDM
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.