The effect of gut microbiota and probiotic organisms on the properties of extended spectrum beta-lactamase producing and carbapenem resistant Enterobacteriaceae including growth, beta-lactamase activity and gene transmissibility.
Anti-Bacterial Agents
/ therapeutic use
Carbapenem-Resistant Enterobacteriaceae
/ drug effects
Carbapenems
/ therapeutic use
Enterobacteriaceae Infections
/ drug therapy
Gastrointestinal Microbiome
/ physiology
Humans
Microbial Sensitivity Tests
/ methods
Probiotics
/ therapeutic use
beta-Lactamases
/ metabolism
Antimicrobial resistant (AMR)
Extended spectrum β-lactamase (ESBL)-Producing Escherichia coli
Gut microbiota
Probiotics
Journal
Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy
ISSN: 1437-7780
Titre abrégé: J Infect Chemother
Pays: Netherlands
ID NLM: 9608375
Informations de publication
Date de publication:
Nov 2019
Nov 2019
Historique:
received:
16
01
2019
revised:
30
03
2019
accepted:
28
04
2019
pubmed:
11
6
2019
medline:
20
2
2020
entrez:
11
6
2019
Statut:
ppublish
Résumé
The gut microbiota may play a pivotal role in controlling the antimicrobial resistant (AMR) organisms although the evidences are limited. We investigated the effects of gut microbiota on the growth of AMR organisms, β-lactamases activity and transmissibility of antimicrobial resistant properties of the extended spectrum β-lactamase (ESBL)-producing Escherichia coli and carbapenem-resistant Enterobacteriaceae. CTX-M-15-positive, ESBL-producing E. coli and carbapenem resistant Enterobacteriaceae, Bacteroides fragilis, Bifidobacterium longum, Clostridium butyricum, Clostridioides difficile, Clostridium perfringens, Enterococcus faecium, Lactobacillus plantarum and probiotic strain of C. butyricum MIYAIRI 588 were used in this study. The growth of AMR organisms was suppressed by the supernatant of C. butyricum, C. difficile, C. perfringens, E. faecium and L. plantarum in a dose dependent manner but not by that of B. fragilis and B. longum. The β-lactamase activity produced by E. coli was reduced by the presence of culture supernatant of certain gut microbiota during stationary phase of E. coli. Importantly, C. butyricum MIYAIRI 588 culture supernatant suppressed the transcription of bla
Identifiants
pubmed: 31178280
pii: S1341-321X(19)30134-5
doi: 10.1016/j.jiac.2019.04.021
pii:
doi:
Substances chimiques
Anti-Bacterial Agents
0
Carbapenems
0
beta-Lactamases
EC 3.5.2.6
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
894-900Informations de copyright
Copyright © 2019 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.