In vitro activity of dalbavancin against Gram-positive bacteria isolated from diabetic foot osteomyelitis.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
15 07 2021
Historique:
received: 28 01 2021
accepted: 15 03 2021
pubmed: 13 4 2021
medline: 11 8 2021
entrez: 12 4 2021
Statut: ppublish

Résumé

Diabetic foot infections (DFIs) represent a serious threat to public health because of their frequency and the severity of their consequences, i.e. osteomyelitis and amputation. The management of diabetic foot osteomyelitis (DFOM) requires prolonged antibiotic therapy. In Western countries, Gram-positive bacteria are the most commonly encountered pathogens. This study evaluated the in vitro activity of dalbavancin, a novel lipoglycopeptide with extended half-life, recently marketed in Europe for acute bacterial skin and skin structure infections, on a panel of Gram-positive bacteria responsible for DFOM. Dalbavancin activity was evaluated against a panel of Gram-positive bacterial strains isolated from bone biopsies performed by a trained surgeon among patients with suspected DFOM. MICs were determined using MIC Test Strips (Liofilchem) and confirmed with the EUCAST broth microdilution method. Three other antimicrobial agents (vancomycin, teicoplanin and ceftobiprole) were used as comparators. Dalbavancin showed excellent activity against all Gram-positive bacterial strains tested, including one teicoplanin-resistant Staphylococcus epidermidis isolate. With MIC50 and MIC90 values of 0.047 and 0.094 mg/L, respectively, dalbavancin showed the most potent in vitro activity among antimicrobial agents tested. With its efficacy, good tolerability and unique pharmacokinetic properties, dalbavancin appears to be a promising treatment for DFOM involving Gram-positive bacteria.

Sections du résumé

BACKGROUND
Diabetic foot infections (DFIs) represent a serious threat to public health because of their frequency and the severity of their consequences, i.e. osteomyelitis and amputation. The management of diabetic foot osteomyelitis (DFOM) requires prolonged antibiotic therapy. In Western countries, Gram-positive bacteria are the most commonly encountered pathogens.
OBJECTIVES
This study evaluated the in vitro activity of dalbavancin, a novel lipoglycopeptide with extended half-life, recently marketed in Europe for acute bacterial skin and skin structure infections, on a panel of Gram-positive bacteria responsible for DFOM.
METHODS
Dalbavancin activity was evaluated against a panel of Gram-positive bacterial strains isolated from bone biopsies performed by a trained surgeon among patients with suspected DFOM. MICs were determined using MIC Test Strips (Liofilchem) and confirmed with the EUCAST broth microdilution method. Three other antimicrobial agents (vancomycin, teicoplanin and ceftobiprole) were used as comparators.
RESULTS
Dalbavancin showed excellent activity against all Gram-positive bacterial strains tested, including one teicoplanin-resistant Staphylococcus epidermidis isolate. With MIC50 and MIC90 values of 0.047 and 0.094 mg/L, respectively, dalbavancin showed the most potent in vitro activity among antimicrobial agents tested.
CONCLUSIONS
With its efficacy, good tolerability and unique pharmacokinetic properties, dalbavancin appears to be a promising treatment for DFOM involving Gram-positive bacteria.

Identifiants

pubmed: 33842980
pii: 6220393
doi: 10.1093/jac/dkab117
doi:

Substances chimiques

Anti-Bacterial Agents 0
Teicoplanin 61036-62-2
dalbavancin 808UI9MS5K

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2057-2060

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Alix Pantel (A)

Virulence Bactérienne et Infections Chroniques, INSERM U1047, Université de Montpellier, Service de Microbiologie et Hygiène Hospitalière, Clinique du Pied Diabétique Gard Occitanie, CHU Nîmes, Nîmes, France.

Oriane Nachar (O)

Service de Microbiologie et Hygiène Hospitalière, CHU Nîmes, Nîmes, France.

Agathe Boudet (A)

Virulence Bactérienne et Infections Chroniques, INSERM U1047, Université de Montpellier, Service de Microbiologie et Hygiène Hospitalière, Clinique du Pied Diabétique Gard Occitanie, CHU Nîmes, Nîmes, France.

Paul Loubet (P)

Virulence Bactérienne et Infections Chroniques, INSERM U1047, Université de Montpellier, Service des Maladies Infectieuses et Tropicales, Clinique du Pied Diabétique Gard Occitanie, CHU Carémeau, Nîmes, France.

Sophie Schuldiner (S)

Virulence Bactérienne et Infections Chroniques, INSERM U1047, Université de Montpellier, Service des Maladies Métaboliques et Endocriniennes, Clinique du Pied Diabétique Gard Occitanie, CHU Carémeau, Nîmes, France.

Nicolas Cellier (N)

Service de Chirurgie Orthopédique, Clinique du Pied Diabétique Gard Occitanie, CHU Carémeau, Nîmes, France.

Albert Sotto (A)

Virulence Bactérienne et Infections Chroniques, INSERM U1047, Université de Montpellier, Service des Maladies Infectieuses et Tropicales, Clinique du Pied Diabétique Gard Occitanie, CHU Carémeau, Nîmes, France.

Catherine Dunyach-Remy (C)

Virulence Bactérienne et Infections Chroniques, INSERM U1047, Université de Montpellier, Service de Microbiologie et Hygiène Hospitalière, Clinique du Pied Diabétique Gard Occitanie, CHU Nîmes, Nîmes, France.

Jean-Philippe Lavigne (JP)

Virulence Bactérienne et Infections Chroniques, INSERM U1047, Université de Montpellier, Service de Microbiologie et Hygiène Hospitalière, Clinique du Pied Diabétique Gard Occitanie, CHU Nîmes, Nîmes, France.

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