| Literature DB >> 34063846 |
Javier Campanini-Salinas1,2, Juan Andrades-Lagos1, Nicolás Hinojosa1, Fabián Moreno1, Pedro Alarcón3, Gerardo González-Rocha4,5, Ian E Burbulis6,7, David Vásquez-Velásquez1.
Abstract
There is an urgent need for the development of new antibiotics. Here, we describe the inhibitory activity of new quinone compounds against methicillin-resistant Staphylococcus aureus (ATCC® 43300), methicillin-sensitive S. aureus (ATCC® 29213), and two clinical isolates from Chile (ISP-213 and ISP-214). We observed 99.9% reduction in viability within 2 h of exposure without the cultures exhibiting any post-antibiotic effect, which was twice the kinetics to that observed with vancomycin. These clinical isolates did not acquire resistance to these quinone derivatives during the course of our study. We found that these compounds protected larvae of the greater wax moth, sp. Galleria mellonella, from infection by these MRSA clinical strains as effectively as vancomycin. These quinone derivatives are potential drug candidates worth further development.Entities:
Keywords: drug discovery; methicillin-resistant S. aureus (MRSA); quinone-antibiotics
Year: 2021 PMID: 34063846 DOI: 10.3390/antibiotics10060614
Source DB: PubMed Journal: Antibiotics (Basel) ISSN: 2079-6382