First Penicillin-Binding Protein Occupancy Patterns for 15 β-Lactams and β-Lactamase Inhibitors in Mycobacterium abscessus

Author:

Sayed Alaa R. M.12,Shah Nirav R.1,Basso Kari B.3,Kamat Manasi3,Jiao Yuanyuan1,Moya Bartolome45,Sutaria Dhruvitkumar S.1,Lang Yinzhi1,Tao Xun1,Liu Weiguo6,Shin Eunjeong1,Zhou Jieqiang1,Werkman Carolin1,Louie Arnold6,Drusano George L.6ORCID,Bulitta Jürgen B.1ORCID

Affiliation:

1. Department of Pharmacotherapy and Translational Research, College of Pharmacy, University of Florida, Orlando, Florida, USA

2. Department of Chemistry, Faculty of Science, Fayoum University, Fayoum, Egypt

3. Department of Chemistry, University of Florida, Gainesville, Florida, USA

4. Servicio de Microbiología, Hospital Universitario Son Espases, Instituto de Investigación Sanitaria Illes Balears, Palma de Mallorca, Spain

5. Unidad de Investigación, Hospital Universitario Son Espases, Instituto de Investigación Sanitaria Illes Balears, Palma de Mallorca, Spain

6. Institute for Therapeutic Innovation, College of Medicine, University of Florida, Orlando, Florida, USA

Abstract

Mycobacterium abscessus causes serious infections that often require over 18 months of antibiotic combination therapy. There is no standard regimen for the treatment of M. abscessus infections, and the multitude of combinations that have been used clinically have had low success rates and high rates of toxicities. With β-lactam antibiotics being safe, double β-lactam and β-lactam/β-lactamase inhibitor combinations are of interest for improving the treatment of M. abscessus infections and minimizing toxicity.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

HHS | NIH | NIH Office of the Director

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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