Dioxane-Linked Novel Bacterial Topoisomerase Inhibitors Exhibit Bactericidal Activity against Planktonic and Biofilm Staphylococcus aureus In Vitro

被引:2
作者
Chen, Anna [1 ]
Dellos-Nolan, Sheri [1 ]
Lu, Yanran [2 ]
West, Jason S. [2 ]
Wozniak, Daniel J. [1 ,3 ]
Mitton-Fry, Mark J. [2 ]
机构
[1] Ohio State Univ, Coll Med, Microbial Infect & Immun, Columbus, OH 43210 USA
[2] Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA
[3] Ohio State Univ, Coll Arts & Sci, Dept Microbiol, Columbus, OH USA
基金
美国国家卫生研究院;
关键词
biofilm; Staphylococcus; topoisomerase; METHICILLIN-RESISTANT; COMBINATION; VANCOMYCIN; SYNERGY; EPIDEMIOLOGY; INFECTIONS; INSIGHTS;
D O I
10.1128/spectrum.02056-22
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The development of novel treatments for Staphylococcus aureus infections remains a high priority worldwide. We previously reported compounds 0147 and 0186, novel bacterial topoisomerase inhibitors (NBTIs) with potent antibacterial activity against S. aureus, including methicillin-resistant S. aureus. Here, we further investigated the in vitro activity of 0147 and 0186 against S. aureus ATCC 29213. Both compounds demonstrated bactericidal activity against planktonic and biofilm S. aureus, which then translated into significant inhibition of biofilm formation. Combinations of NBTIs and glycopeptides yielded indifferent interactions against planktonic S. aureus, but several had synergistic effects against S. aureus biofilms. This work reinforces the potential of NBTIs as future therapeutics for S. aureus infections.
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收藏
页数:9
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