Systematic analysis of drug combinations against Gram-positive bacteria

被引:0
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作者
Elisabetta Cacace
Vladislav Kim
Vallo Varik
Michael Knopp
Manuela Tietgen
Amber Brauer-Nikonow
Kemal Inecik
André Mateus
Alessio Milanese
Marita Torrissen Mårli
Karin Mitosch
Joel Selkrig
Ana Rita Brochado
Oscar P. Kuipers
Morten Kjos
Georg Zeller
Mikhail M. Savitski
Stephan Göttig
Wolfgang Huber
Athanasios Typas
机构
[1] Genome Biology Unit,European Molecular Biology Laboratory
[2] Collaboration for joint PhD degree between EMBL and Heidelberg University,European Molecular Biology Laboratory
[3] Faculty of Biosciences,Faculty of Chemistry, Biotechnology and Food Science
[4] Goethe University Frankfurt,Cluster of Excellence EXC 2124 Controlling Microbes to Fight Infections
[5] University Hospital,Department of Molecular Genetics, Groningen Molecular Biology and Biotechnology Institute
[6] Institute for Medical Microbiology and Infection Control,Institute of Medical Microbiology
[7] Structural and Computational Biology Unit,Interfaculty Institute of Microbiology and Infection Medicine
[8] Department of Biology,undefined
[9] Institute of Microbiology,undefined
[10] and Swiss Institute of Bioinformatics,undefined
[11] ETH Zurich,undefined
[12] Norwegian University of Life Sciences,undefined
[13] University of Tübingen,undefined
[14] University of Groningen,undefined
[15] University Hospital of RWTH,undefined
[16] University of Tübingen,undefined
来源
Nature Microbiology | 2023年 / 8卷
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摘要
Drug combinations can expand options for antibacterial therapies but have not been systematically tested in Gram-positive species. We profiled ~8,000 combinations of 65 antibacterial drugs against the model species Bacillus subtilis and two prominent pathogens, Staphylococcus aureus and Streptococcus pneumoniae. Thereby, we recapitulated previously known drug interactions, but also identified ten times more novel interactions in the pathogen S. aureus, including 150 synergies. We showed that two synergies were equally effective against multidrug-resistant S. aureus clinical isolates in vitro and in vivo. Interactions were largely species-specific and synergies were distinct from those of Gram-negative species, owing to cell surface and drug uptake differences. We also tested 2,728 combinations of 44 commonly prescribed non-antibiotic drugs with 62 drugs with antibacterial activity against S. aureus and identified numerous antagonisms that might compromise the efficacy of antimicrobial therapies. We identified even more synergies and showed that the anti-aggregant ticagrelor synergized with cationic antibiotics by modifying the surface charge of S. aureus. All data can be browsed in an interactive interface (https://apps.embl.de/combact/).
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页码:2196 / 2212
页数:16
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