In Vitro Activity of CEM-102 (fusidic Acid) Against Prevalent Clones and Resistant Phenotypes of Staphylococcus Aureus
Overview
Authors
Affiliations
Clinical development of CEM-102 (fusidic acid) has recently begun in the United States for chronic oral treatment of prosthetic joint infections. To support this development, the in vitro activity of fusidic acid against important Staphylococcus aureus clones and resistance phenotypes was determined. Against 51 such isolates, the modal fusidic acid MIC was 0.12 μg/ml (range, 0.06 to 0.25 μg/ml for 49 isolates). This level of in vitro fusidic acid activity underscores the potential clinical utility of this compound in the United States.
The implication of Mycobacterium tuberculosis-mediated metabolism of targeted xenobiotics.
Singh V, Dziwornu G, Chibale K Nat Rev Chem. 2023; 7(5):340-354.
PMID: 37117810 PMC: 10026799. DOI: 10.1038/s41570-023-00472-3.
Crystal Structure of Elongation Factor G1.
Gao X, Yu X, Zhu K, Qin B, Wang W, Han P Front Mol Biosci. 2021; 8:667638.
PMID: 34540889 PMC: 8446442. DOI: 10.3389/fmolb.2021.667638.
Hajikhani B, Goudarzi M, Kakavandi S, Amini S, Zamani S, van Belkum A Antimicrob Resist Infect Control. 2021; 10(1):75.
PMID: 33933162 PMC: 8088720. DOI: 10.1186/s13756-021-00943-6.
Siala W, Rodriguez-Villalobos H, Fernandes P, Tulkens P, Van Bambeke F Antimicrob Agents Chemother. 2018; 62(7).
PMID: 29712650 PMC: 6021669. DOI: 10.1128/AAC.00598-18.
Fernandes P Cold Spring Harb Perspect Med. 2016; 6(1):a025437.
PMID: 26729758 PMC: 4691801. DOI: 10.1101/cshperspect.a025437.