Systematic analysis of drug combinations against Gram-positive bacteria

被引:20
|
作者
Cacace, Elisabetta [1 ]
Kim, Vladislav [1 ,2 ]
Varik, Vallo [1 ]
Knopp, Michael [1 ]
Tietgen, Manuela [3 ]
Brauer-Nikonow, Amber [1 ]
Inecik, Kemal [1 ]
Mateus, Andre [1 ]
Milanese, Alessio [4 ,5 ,6 ]
Marli, Marita Torrissen [7 ]
Mitosch, Karin [1 ]
Selkrig, Joel [1 ,10 ]
Brochado, Ana Rita [1 ,8 ,11 ]
Kuipers, Oscar P. [9 ]
Kjos, Morten [7 ]
Zeller, Georg [4 ]
Savitski, Mikhail M. [1 ]
Goettig, Stephan [3 ]
Huber, Wolfgang [1 ]
Typas, Athanasios [1 ,4 ]
机构
[1] Genome Biol Unit, European Mol Biol Lab, Heidelberg, Germany
[2] Collaborat joint PhD degree EMBL & Heidelberg Univ, Fac Biosci, Heidelberg, Germany
[3] Goethe Univ Frankfurt, Univ Hosp, Inst Med Microbiol & Infect Control, Frankfurt, Germany
[4] European Mol Biol Lab, Struct & Computat Biol Unit, Heidelberg, Germany
[5] Inst Microbiol, Dept Biol, Zurich, Switzerland
[6] Swiss Fed Inst Technol, Swiss Inst Bioinformat, Zurich, Switzerland
[7] Norwegian Univ Life Sci, Fac Chem Biotechnol & Food Sci, As, Norway
[8] Univ Tubingen, Cluster Excellence EXC 2124 Controlling Microbes F, Tubingen, Germany
[9] Univ Groningen, Groningen Mol Biol & Biotechnol Inst, Dept Mol Genet, Groningen, Netherlands
[10] Univ Hosp RWTH, Inst Med Microbiol, Aachen, Germany
[11] Univ Tubingen, Interfac Inst Microbiol & Infect Med, Tubingen, Germany
基金
瑞典研究理事会;
关键词
WALL TEICHOIC-ACID; STAPHYLOCOCCUS-AUREUS; ANTIBIOTIC-THERAPY; ESCHERICHIA-COLI; BINDING PROTEINS; GENOME SEQUENCE; UNITED-STATES; AMINOGLYCOSIDES; IDENTIFICATION; ANTAGONISM;
D O I
10.1038/s41564-023-01486-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Drug combinations can expand options for antibacterial therapies but have not been systematically tested in Gram-positive species. We profiled similar to 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/).
引用
收藏
页码:2196 / +
页数:37
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