Evidence map›Paper›PMID 37055536›Full record

ArticleCommunications biology2023

Synthesis of vancomycin fluorescent probes that retain antimicrobial activity, identify Gram-positive bacteria, and detect Gram-negative outer membrane damage.

Bing Zhang, Wanida Phetsang, M Rhia L Stone, Sanjaya Kc, Mark S Butler, Matthew A Cooper, Alysha G Elliott, Urszula Łapińska, Margaritis Voliotis, Krasimira Tsaneva-Atanasova and 2 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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  14. Synthesis and preclinical evaluation of novelEuropean journal of nuclear medicine and molecular imaging · 2024
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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

12 authors at 3 institutions in 3 countries.

Bing ZhangCentre for Superbug Solutions, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia.ORCID 0000-0001-8405-9242
Wanida PhetsangCentre for Superbug Solutions, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia.
M Rhia L StoneCentre for Superbug Solutions, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia.
Sanjaya KcCentre for Superbug Solutions, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia.
Mark S ButlerCentre for Superbug Solutions, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia.
Matthew A CooperCentre for Superbug Solutions, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia.ORCID 0000-0003-3147-3460
Alysha G ElliottCentre for Superbug Solutions, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia.ORCID 0000-0002-2983-0484
Urszula ŁapińskaLiving Systems Institute, University of Exeter, Stocker Road, Exeter, EX4 4QD, UK.
Margaritis VoliotisLiving Systems Institute, University of Exeter, Stocker Road, Exeter, EX4 4QD, UK.
Krasimira Tsaneva-AtanasovaLiving Systems Institute, University of Exeter, Stocker Road, Exeter, EX4 4QD, UK.ORCID 0000-0002-6294-7051
Stefano PagliaraLiving Systems Institute, University of Exeter, Stocker Road, Exeter, EX4 4QD, UK.ORCID 0000-0001-9796-1956
Mark A T BlaskovichCentre for Superbug Solutions, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia. m.blaskovich@uq.edu.au.ORCID 0000-0001-9447-2292
The University of Queensland · AUUniversity of Exeter · GBEngineering and Physical Sciences Research Council · GB

Funding

Biotechnology and Biological Sciences Research Council BB/V008021/1Medical Research Council MCPC17189Wellcome TrustWellcome Trust WT1104797/Z/14/Z
6 · The paper itself

Abstract

Antimicrobial resistance is an urgent threat to human health, and new antibacterial drugs are desperately needed, as are research tools to aid in their discovery and development. Vancomycin is a glycopeptide antibiotic that is widely used for the treatment of Gram-positive infections, such as life-threatening systemic diseases caused by methicillin-resistant Staphylococcus aureus (MRSA). Here we demonstrate that modification of vancomycin by introduction of an azide substituent provides a versatile intermediate that can undergo copper-catalysed azide-alkyne cycloaddition (CuAAC) reaction with various alkynes to readily prepare vancomycin fluorescent probes. We describe the facile synthesis of three probes that retain similar antibacterial profiles to the parent vancomycin antibiotic. We demonstrate the versatility of these probes for the detection and visualisation of Gram-positive bacteria by a range of methods, including plate reader quantification, flow cytometry analysis, high-resolution microscopy imaging, and single cell microfluidics analysis. In parallel, we demonstrate their utility in measuring outer-membrane permeabilisation of Gram-negative bacteria. The probes are useful tools that may facilitate detection of infections and development of new antibiotics.

Indexed as

Methicillin-Resistant Staphylococcus aureusVancomycinAnti-Bacterial AgentsAzidesFluorescent DyesGram-Positive BacteriaHumansAnti-Bacterial AgentsAzidesFluorescent DyesVancomycin

Identifiers

PMID37055536
PMCPMC10102067
OpenAlexW4365479748

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.