Antimicrobial and antibiofilm activities of chromone derivatives against uropathogenic Escherichia coli.
Animals
Uropathogenic Escherichia coli
/ physiology
Siderophores
/ metabolism
Caenorhabditis elegans
Urinary Tract Infections
/ pathology
Anti-Infective Agents
/ metabolism
Virulence Factors
/ genetics
Biofilms
Chromones
/ metabolism
Escherichia coli Infections
/ drug therapy
Escherichia coli Proteins
/ genetics
Biofilm
Chromones
E. coli
UPEC
Virulence
Journal
Microbiological research
ISSN: 1618-0623
Titre abrégé: Microbiol Res
Pays: Germany
ID NLM: 9437794
Informations de publication
Date de publication:
Jan 2024
Jan 2024
Historique:
received:
05
07
2023
revised:
13
10
2023
accepted:
24
10
2023
medline:
28
11
2023
pubmed:
6
11
2023
entrez:
3
11
2023
Statut:
ppublish
Résumé
Uropathogenic Escherichia coli (UPEC) is a urinary tract pathogen responsible for most nosocomial urinary tract infections and can cause severe conditions like acute cystitis of the bladder or pyelonephritis. UPEC harbors a host of virulence factors like curli, hemolysin, siderophore, and motility factors and can form biofilm-like communities and quiescent reservoirs that aid its survival. This study was performed to investigate the antibiofilm, antimicrobial, and antivirulence potentials of three chromone derivatives, namely, 6-bromo 3-formylchromone, 6-chloro 3-formylchromone, and 3-formyl 6-isopropylchromone. These chromones had MICs against UPEC of 20, 20, and 50 µg/ml, respectively, inhibited biofilm formation by 72-96% at 20 µg/ml, and inhibited UPEC-associated virulence factors, that is, hemolysis, motility, curli, siderophore production, indole production, quiescent colony formation, and cell surface hydrophobicity. Gene expression analysis indicated these three derivatives downregulated virulence genes associated with toxins, biofilm production, and stress regulation and suggested they might target two-component UvrY response regulator. 3D-QSAR analysis showed that substitutions at the third and sixth positions of the chromone scaffold favor antimicrobial activity against UPEC. Furthermore, ADME profiles and C. elegans cytotoxicity assays indicated that these chromone derivatives are potent, safe drug candidates.
Identifiants
pubmed: 37922697
pii: S0944-5013(23)00239-2
doi: 10.1016/j.micres.2023.127537
pii:
doi:
Substances chimiques
Siderophores
0
Anti-Infective Agents
0
Virulence Factors
0
Chromones
0
Escherichia coli Proteins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
127537Informations de copyright
Copyright © 2023 Elsevier GmbH. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no conflict of interest.