Evidence map›Paper›PMID 37047217›Full record

ArticleInternational journal of molecular sciences2023

Identification of a Small Molecule Compound Active against Antibiotic-Tolerant

Ho-Ting-Venice Iu, Pak-Ming Fong, Hin-Cheung-Bill Yam, Peng Gao, Bingpeng Yan, Pok-Man Lai, Victor-Yat-Man Tang, Ka-Ho Li, Chi-Wang Ma, King-Hei-Kenneth Ng and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Mini review: Persister cell control strategies.Frontiers in pharmacology · 2025
    Review
  5. 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

14 authors at 3 institutions in 2 countries.

Ho-Ting-Venice IuDepartment of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.ORCID 0000-0002-7612-0864
Pak-Ming FongMorningside Laboratory for Chemical Biology, Department of Chemistry, The University of Hong Kong, Hong Kong, China.ORCID 0009-0009-1085-1603
Hin-Cheung-Bill YamDepartment of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Peng GaoDepartment of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.ORCID 0000-0002-6877-6388
Bingpeng YanDepartment of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.ORCID 0000-0001-5964-2508
Pok-Man LaiDepartment of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Victor-Yat-Man TangDepartment of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Ka-Ho LiDepartment of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Chi-Wang MaMorningside Laboratory for Chemical Biology, Department of Chemistry, The University of Hong Kong, Hong Kong, China.ORCID 0000-0002-6785-5148
King-Hei-Kenneth NgMorningside Laboratory for Chemical Biology, Department of Chemistry, The University of Hong Kong, Hong Kong, China.
Kong-Hung SzeDepartment of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Dan YangMorningside Laboratory for Chemical Biology, Department of Chemistry, The University of Hong Kong, Hong Kong, China.ORCID 0000-0002-1726-9335
Julian DaviesDepartment of Microbiology and Immunology, The University of British Columbia, Vancouver, BC V6T 1Z3, Canada.
Richard-Yi-Tsun KaoDepartment of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Chinese University of Hong Kong · HKUniversity of Hong Kong · HKUniversity of British Columbia · CA

Funding

HMRF Commissioned Study Project Grant CID-HKU1-14RGC of the Hong Kong SAR Projects AoE AoE/P-705/16RGC of the Hong Kong SAR Projects GRF 17104420
6 · The paper itself

Abstract

Antibiotic tolerance poses a threat to current antimicrobial armamentarium. Bacteria at a tolerant state survive in the presence of antibiotic treatment and account for persistence, relapse and recalcitrance of infections. Antibiotic treatment failure may occur due to antibiotic tolerance. Persistent infections are difficult to treat and are often associated with poor prognosis, imposing an enormous burden on the healthcare system. Effective strategies targeting antibiotic-tolerant bacteria are therefore highly warranted. In this study, small molecule compound SA-558 was identified to be effective against

Indexed as

Methicillin-Resistant Staphylococcus aureusStaphylococcal InfectionsAdenosine TriphosphateAnimalsAnti-Bacterial AgentsBacteriaHumansMiceMicrobial Sensitivity TestsStaphylococcus aureusVancomycinAdenosine TriphosphateAnti-Bacterial AgentsVancomycinadjuvantsantibiotic toleranceMRSApersistent infectionspersister

Identifiers

PMID37047217
PMCPMC10094146
OpenAlexW4361007469

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.