UPLC/Q-TOF-MS-based metabolomics and molecular docking analysis of Bifidobacterium adolescentis exposure to levofloxacin.

Bifidobacterium adolescentis antibiotic‐associated diarrhea levofloxacin metabolomics molecular docking

Journal

Biomedical chromatography : BMC
ISSN: 1099-0801
Titre abrégé: Biomed Chromatogr
Pays: England
ID NLM: 8610241

Informations de publication

Date de publication:
29 Apr 2024
Historique:
revised: 04 02 2024
received: 02 11 2023
accepted: 26 02 2024
medline: 30 4 2024
pubmed: 30 4 2024
entrez: 29 4 2024
Statut: aheadofprint

Résumé

Antibiotic-associated diarrhea is a common adverse reaction caused by the widespread use of antibiotics. The decrease in probiotics is one of the reasons why antibiotics cause drug-induced diarrhea. However, few studies have addressed the intrinsic mechanism of antibiotics inhibiting probiotics. To investigate the underlying mechanism of levofloxacin against Bifidobacterium adolescentis, we used a metabolomics mass spectrometry-based approach and molecular docking analysis for a levofloxacin-induced B. adolescentis injury model. The results showed that levofloxacin reduced the survival rate of B. adolescentis and decreased the number of B. adolescentis. The untargeted metabolomics analysis identified 27 potential biomarkers, and many of these metabolites are involved in energy metabolism, amino acid metabolism and the lipid metabolism pathway. Molecular docking showed that levofloxacin can bind with aminoacyl-tRNA synthetase and lactic acid dehydrogenase. This result provides a novel insight into the mechanism of the adverse reactions of levofloxacin.

Identifiants

pubmed: 38684194
doi: 10.1002/bmc.5862
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e5862

Subventions

Organisme : National Natural Science Foundation of China

Informations de copyright

© 2024 John Wiley & Sons Ltd.

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Auteurs

Shisui Feng (S)

Pharmaceutical College, Guangxi Medical University, Nanning, China.
The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.

Yue Guo (Y)

Pharmaceutical College, Guangxi Medical University, Nanning, China.
School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.

Qianyi Wang (Q)

Department of pharmacy, Guangxi Medical University Cancer Hospital, Nanning, China.

Mingwei Meng (M)

Pharmaceutical College, Guangxi Medical University, Nanning, China.

Xi Liu (X)

Pharmaceutical College, Guangxi Medical University, Nanning, China.

Chi Zhang (C)

Pharmaceutical College, Guangxi Medical University, Nanning, China.

Hua Zheng (H)

Life Sciences Institute, Guangxi Medical University, Nanning, China.

Hongwei Guo (H)

Pharmaceutical College, Guangxi Medical University, Nanning, China.

Rigang Lu (R)

Guangxi Institute for Food and Drug Control, Nanning, China.

Danfeng Li (D)

Guangxi Institute for Food and Drug Control, Nanning, China.

Zhiheng Su (Z)

Pharmaceutical College, Guangxi Medical University, Nanning, China.

Hui Song (H)

Pharmaceutical College, Guangxi Medical University, Nanning, China.

Yonghong Liang (Y)

Pharmaceutical College, Guangxi Medical University, Nanning, China.

Classifications MeSH