Valorization of Invasive Plant Extracts against the Bispecies Biofilm

Candida albicans Staphylococcus aureus antibiofilm betulinic acid invasive plants molecular networking natural products

Journal

Antibiotics (Basel, Switzerland)
ISSN: 2079-6382
Titre abrégé: Antibiotics (Basel)
Pays: Switzerland
ID NLM: 101637404

Informations de publication

Date de publication:
11 Nov 2022
Historique:
received: 21 10 2022
revised: 07 11 2022
accepted: 09 11 2022
entrez: 24 11 2022
pubmed: 25 11 2022
medline: 25 11 2022
Statut: epublish

Résumé

Invasive plants efficiently colonize non-native territories, suggesting a great production of bioactive metabolites which could be effective antibiofilm weapons. Our study aimed to look for original molecules able to inhibit bispecies biofilm formed by S. aureus and C. albicans. Extracts from five invasive macrophytes (Ludwigia peploides, Ludwigia grandiflora, Myriophyllum aquaticum, Lagarosiphon major and Egeria densa) were prepared and tested in vitro against 24 h old bispecies biofilms using a crystal violet staining (CVS) assay. The activities of the extracts reducing the biofilm total biomass by 50% or more were comparatively analyzed against each microbial species forming the biofilm by flow cytometry (FCM) and scanning electron microscopy. Extracts active against both species were fractionated. Obtained fractions were analyzed by UHPLC-MS/MS and evaluated by the CVS assay. Chemical and biological data were combined into a bioactivity-based molecular networking (BBMN) to identify active compounds. The aerial stem extract of L. grandiflora showed the highest antibiofilm activity (>50% inhibition at 50 µg∙mL−1). The biological, chemical and BBMN investigations of its fractions highlighted nine ions correlated with the antibiofilm activity. The most correlated compound, identified as betulinic acid (BA), inhibited bispecies biofilms regardless of the three tested couples of strains (ATCC strains: >40% inhibition, clinical isolates: ≈27% inhibition), confirming its antibiofilm interest.

Identifiants

pubmed: 36421241
pii: antibiotics11111595
doi: 10.3390/antibiotics11111595
pmc: PMC9686625
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Region Nouvelle-Aquitaine
ID : AAPR2020-2019-8408110 - Research Grant
Organisme : Bordeaux Metabolome Facility
ID : ANR-11-INBS-0010
Organisme : University of Poitiers and University of Limoges
ID : AAP ARIC 2019 Research grant
Organisme : 2015-2020 State-Region Planning Contracts (CPER)
ID : XX
Organisme : European Regional Development Fund (FEDER)
ID : XX
Organisme : Centre National de la Recherche Scientifique
ID : XX

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Auteurs

Guillaume Hamion (G)

Laboratoire EBI, University of Poitiers, UMR CNRS 7267, F-86000 Poitiers, France.

Willy Aucher (W)

Laboratoire EBI, University of Poitiers, UMR CNRS 7267, F-86000 Poitiers, France.

Charles Tardif (C)

University of Bordeaux, UMR INRAE 1366, Bordeaux INP, OENO, ISVV, F-33140 Villenave d'Ornon, France.
Bordeaux Sciences Agro, UMR INRAE 1366, Bordeaux INP, OENO, ISVV, F-33170 Gradignan, France.

Julie Miranda (J)

University of Bordeaux, UMR INRAE 1366, Bordeaux INP, OENO, ISVV, F-33140 Villenave d'Ornon, France.
Bordeaux Sciences Agro, UMR INRAE 1366, Bordeaux INP, OENO, ISVV, F-33170 Gradignan, France.

Caroline Rouger (C)

University of Bordeaux, UMR INRAE 1366, Bordeaux INP, OENO, ISVV, F-33140 Villenave d'Ornon, France.
Bordeaux Sciences Agro, UMR INRAE 1366, Bordeaux INP, OENO, ISVV, F-33170 Gradignan, France.
Bordeaux Metabolome, MetaboHUB, PHENOME-EMPHASIS, Centre INRAE de Nouvelle Aquitaine-Bordeaux, F-33140 Villenave d'Ornon, France.

Christine Imbert (C)

Laboratoire EBI, University of Poitiers, UMR CNRS 7267, F-86000 Poitiers, France.

Marion Girardot (M)

Laboratoire EBI, University of Poitiers, UMR CNRS 7267, F-86000 Poitiers, France.

Classifications MeSH