Acacia senegal Budmunchiamines as a Potential Adjuvant for Rejuvenating Phenicol Activities towards Escherichia coli-Resistant Strains

Author:

Dofini Magnini René123ORCID,Pedinielli François4ORCID,Vergalli Julia1ORCID,Ouedraogo Noufou2,Remy Simon4,Hilou Adama3,Brunel Jean-Michel1ORCID,Pagès Jean-Marie1ORCID,Davin-Regli Anne1ORCID

Affiliation:

1. UMR_MD1, U-1261, INSERM, SSA, IRBA, MCT, Faculté de Pharmacie, Université Aix-Marseille, 13385 Marseille, France

2. Laboratoire de Recherche-Développement de Phytomédicaments et Médicaments (LR-D/PM), IRSS, CNRST, Département MEPHATRA-PH, Ouagadougou 03 BP 7047, Burkina Faso

3. Laboratoire de Biochimie et de Chimie Appliquée (LABIOCA), Université Joseph Ki-Zerbo, Ouagadougou 03 BP 7021, Burkina Faso

4. Institut de Chimie Moléculaire de Reims, UMR CNRS 7312, Université Reims-Champagne-Ardenne, UFR Sciences, BP 1039, CEDEX 2, 51687 Reims, France

Abstract

The continuous emergence of bacterial resistance alters the activities of different antibiotic families and requires appropriate strategies to solve therapeutic impasses. Medicinal plants are an attractive source for researching alternative and original therapeutic molecules. In this study, the fractionation of natural extracts from A. senegal and the determination of antibacterial activities are associated with molecular networking and tandem mass spectrometry (MS/MS) data used to characterize active molecule(s). The activities of the combinations, which included various fractions plus an antibiotic, were investigated using the “chessboard” test. Bio-guided fractionation allowed the authors to obtain individually active or synergistic fractions with chloramphenicol activity. An LC-MS/MS analysis of the fraction of interest and molecular array reorganization showed that most identified compounds are Budmunchiamines (macrocyclic alkaloids). This study describes an interesting source of bioactive secondary metabolites structurally related to Budmunchiamines that are able to rejuvenate a significant chloramphenicol activity in strains that produce an AcrB efflux pump. They will pave the way for researching new active molecules for restoring the activity of antibiotics that are substrates of efflux pumps in enterobacterial-resistant strains.

Funder

MU University, INSERM, Campus France and the French Embassy

AMU University and INSERM

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Reference33 articles.

1. CDC (2019). Antibiotic Resistance Threats in the United States, 2019.

2. OMS (2022). Global Antimicrobial Resistance and Use Surveillance System (GLASS) Report 2022.

3. O’Neill, J. (2016). Tackling Drug-Resistant Infections Globally: Final Report and Recommendations.

4. Mechanisms of Envelope Permeability and Antibiotic Influx and Efflux in Gram-Negative Bacteria;Masi;Nat. Microbiol.,2017

5. OMS (2019). Who Global Report on Traditional and Complementary Medicine 2019.

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