(p)ppGpp/GTP and Malonyl-CoA Modulate Staphylococcus aureus Adaptation to FASII Antibiotics and Provide a Basis for Synergistic Bi-Therapy
Author:
Affiliation:
1. Micalis Institute, INRAE, AgroParisTech, Université Paris-Saclay, Jouy en Josas, France
2. Unité de Biologie des Pathogènes à Gram-positif, CNRS UMR 2001, Institut Pasteur, Paris, France
3. Université de Paris, CNRS UMR8601, Paris, France
Abstract
Funder
DIM Malinf (Domaine d'Intérêt Majeur, Maladies Infectieuses) from the Conseil Régional d'Ile-de-France
Agence Nationale de la Recherche
Fondation pour la Recherche Médicale
French Government Investissement d'Avenir program, Laboratoire d'Excellence Integrative Biology of Emerging Infectious Diseases
Publisher
American Society for Microbiology
Subject
Virology,Microbiology
Link
https://journals.asm.org/doi/pdf/10.1128/mBio.03193-20
Reference50 articles.
1. Strategies to Combat Antimicrobial Resistance
2. Inhibitors of FabI, an Enzyme Drug Target in the Bacterial Fatty Acid Biosynthesis Pathway
3. Type II fatty acid synthesis is not a suitable antibiotic target for Gram-positive pathogens
4. Environmental fatty acids enable emergence of infectious Staphylococcus aureus resistant to FASII-targeted antimicrobials
5. Permissive Fatty Acid Incorporation Promotes Staphylococcal Adaptation to FASII Antibiotics in Host Environments
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