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Glycopeptides revisited | 16681
Journal of Drug Metabolism & Toxicology

Journal of Drug Metabolism & Toxicology
Open Access

ISSN: 2157-7609

Glycopeptides revisited


World Congress and Exhibition on Antibiotics

September 14-16, 2015 Las Vegas, USA

Jon B Bruss

Theravance Biopharma, USA

Scientific Tracks Abstracts: J Drug Metab Toxicol

Abstract :

Vancomycin was isolated from soil from the jungles of Borneo in 1953 by scientists at Eli Lily & Co. It is a naturally occurring antibiotic produced by the soil bacterium Amycolatopsis orientalis (formerly Nocardia orientalis). It was approved in 1958 by the US FDA to treat penicillin resistant staphylococci. Vancomycin has subsequently become a primary treatment for infections due to MRSA; however it is steadily losing potency due to increasing minimum inhibitory concentrations for many strains of MRSA. Since the discovery of vancomycin, several other glycopeptide, lipodepsipeptide, and lipoglycopeptide antibiotics, all members of this class, have been discovered or synthesized including bleomycin (1966), teicoplanin (1975), ramoplanin (1984), dalbavancin (1996), oritavancin (1996), and telavancin (2000). Some of the newer semisynthetic members of this class have multiple mechanisms of action and greater potency against a wider spectrum of gram-positive pathogens, including those with reduced susceptibility to vancomycin. This presentation will describe the various members of this class and compare their attributes and clinical use. Emphasis will be placed on the declining utility of vancomycin and the advantages of the newer lipoglycopeptides.

Biography :

Bruss completed his MD at the University of New Mexico School of Medicine. He completed a pediatric residency at the Children’s Hospital of New Mexico and a fellowship in infectious diseases at Boston Children’s Hospital and Harvard University. Other degrees include a Master of Science in Public Health from Tulane University School of Public Health and a Master of Business Administration from Northwestern University Kellogg School of Business. He held academic positions at Harvard University and University of Washignton. He has experience in clinical drug development, including work with seven classes of antibiotics, multiple anti-virals, anti-fungals, vaccines and biologics.

Email: jbruss@theravance.com

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