Evidence map›Paper›PMID 39636460›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2024

Investigation of antibacterial mode of action of ω-aminoalkoxylxanthones by NMR-based metabolomics and molecular docking.

Paola Dias de Oliveira, Allana Cristina Faustino Martins, Roberto da Silva Gomes, Adilson Beatriz, Glaucia Braz Alcantara, Ana Camila Micheletti

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Article in Metabolomics : Official journal of the Metabolomic Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Paola Dias de OliveiraLP2 Laboratory, Institute of Chemistry, Federal University of Mato Grosso Do Sul, Campo Grande, Brazil.
Allana Cristina Faustino MartinsDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, ND, USA.
Roberto da Silva GomesDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, ND, USA.
Adilson BeatrizLP2 Laboratory, Institute of Chemistry, Federal University of Mato Grosso Do Sul, Campo Grande, Brazil.
Glaucia Braz AlcantaraLP2 Laboratory, Institute of Chemistry, Federal University of Mato Grosso Do Sul, Campo Grande, Brazil. glaucia.alcantara@ufms.br.
Ana Camila MichelettiLP2 Laboratory, Institute of Chemistry, Federal University of Mato Grosso Do Sul, Campo Grande, Brazil. ana.micheletti@ufms.br.

Funding

Brazilian Council for Scientific and Technological Development (CNPq) 427221/2018-8Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brazil (CAPES) Finance code 001Fundação de Apoio ao Desenvolvimento do Ensino, Ciência e Tecnologia do Estado de Mato Grosso do Sul (FUNDECT-MS) 310/2022, 335/2022
6 · The paper itself

Abstract

introductionThe knowledge of the mode of action of an antimicrobial is essential for drug development and helps to fight against bacterial resistance. Thus, it is crucial to use analytical techniques to study the mechanism of action of substances that have potential to act as antibacterial agents

objectiveTo use NMR-based metabolomics combined with chemometrics and molecular docking to identify the metabolic responses of Staphylococcus aureus following exposure to commercial antibiotics and some synthesized ω-aminoalkoxylxanthones.

methodsIntracellular metabolites of S. aureus were extracted after treatment with four commercial antibiotics and three synthesized ω-aminoalkoxylxanthones. NMR spectra were obtained and

resultsThrough chemometric analysis, we distinguished between the control group and antibiotics with extracellular (ampicillin) and intracellular targets (kanamycin, tetracycline, and ciprofloxacin). We identified 21 metabolites, including important metabolites that differentiate the groups, such as betaine, acetamide, glutamate, lysine, alanine, isoleucine/leucine, acetate, threonine, proline, and ethanol. Regarding the xanthone-type derivatives (S6, S7 and S8), we observed a greater similarity between S7 and ciprofloxacin, which targets bacterial DNA replication. The molecular docking analysis showed high affinity of the ω-aminoalkoxylxanthones with the topoisomerase IV enzyme, as well as ciprofloxacin.

conclusionNMR-based metabolomics has shown to be an effective technique to assess the metabolic profile of S. aureus after treatment with certain antimicrobial compounds, helping the investigation of their mechanism of action.

Indexed as

Anti-Bacterial AgentsMagnetic Resonance SpectroscopyMetabolomicsMolecular Docking SimulationStaphylococcus aureusXanthonesMicrobial Sensitivity TestsAnti-Bacterial AgentsXanthonesAntibiotic resistanceMechanism of actionMetabolomeTopoisomeraseXanthones

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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.