{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,5]],"date-time":"2026-08-05T02:05:40Z","timestamp":1785895540800,"version":"3.56.0"},"reference-count":54,"publisher":"American Society for Microbiology","issue":"10","license":[{"start":{"date-parts":[[2024,10,16]],"date-time":"2024-10-16T00:00:00Z","timestamp":1729036800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2024,10,16]],"date-time":"2024-10-16T00:00:00Z","timestamp":1729036800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"DOI":"10.13039\/501100002661","name":"Fonds De La Recherche Scientifique - FNRS","doi-asserted-by":"crossref","award":["PDR T.0190.20"],"award-info":[{"award-number":["PDR T.0190.20"]}],"id":[{"id":"10.13039\/501100002661","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/501100002910","name":"F\u00e9d\u00e9ration Wallonie-Bruxelles","doi-asserted-by":"crossref","award":["FSR-S-SS-19\/18, FSR-S-SS-21\/41"],"award-info":[{"award-number":["FSR-S-SS-19\/18, FSR-S-SS-21\/41"]}],"id":[{"id":"10.13039\/501100002910","id-type":"DOI","asserted-by":"crossref"}]},{"name":"EC | European Research Council","award":["647197"],"award-info":[{"award-number":["647197"]}]},{"DOI":"10.13039\/100009139","name":"Deutsches Zentrum f\u00fcr Infektionsforschung","doi-asserted-by":"crossref","award":["TTU 09.826"],"award-info":[{"award-number":["TTU 09.826"]}],"id":[{"id":"10.13039\/100009139","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/501100001659","name":"Deutsche Forschungsgemeinschaft","doi-asserted-by":"crossref","award":["TRR 261 project 398967434"],"award-info":[{"award-number":["TRR 261 project 398967434"]}],"id":[{"id":"10.13039\/501100001659","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["mBio"],"published-print":{"date-parts":[[2024,10,16]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:sec>\n            <jats:title\/>\n            <jats:p>\n              Infections with multidrug-resistant bacteria pose a major healthcare problem which urges the need for novel treatment options. Besides its potent antiplatelet properties, ticagrelor has antibacterial activity against Gram-positive bacteria, including methicillin- and vancomycin-resistant\n              <jats:italic>Staphylococcus aureus<\/jats:italic>\n              (MRSA and VRSA). Several retrospective studies in cardiovascular patients support an antibacterial effect of this drug which is not related to its antiplatelet activity. We investigated the mechanism of action of ticagrelor in\n              <jats:italic>Staphylococcus aureus<\/jats:italic>\n              and model\n              <jats:italic>Bacillus subtilis,<\/jats:italic>\n              and assessed cross-resistance with two conventional anti-MRSA antibiotics, vancomycin and daptomycin.\n              <jats:italic>Bacillus subtilis<\/jats:italic>\n              bioreporter strains revealed ticagrelor-induced cell envelope-related stress responses. Sub-inhibitory drug concentrations caused membrane depolarization, impaired positioning of both the peripheral membrane protein MinD and the peptidoglycan precursor lipid II, and it affected cell shape. At the MIC, ticagrelor destroyed membrane integrity, indicated by the influx of membrane impermeable dyes, and lipid aggregate formation. Whole-genome sequencing of\n              <jats:italic>in vitro<\/jats:italic>\n              -generated ticagrelor-resistant MRSA clones revealed mutations in genes encoding ClpP, ClpX, and YjbH. Lipidomic analysis of resistant clones displayed changes in levels of the most abundant lipids of the\n              <jats:italic>Staphylococcus aureus<\/jats:italic>\n              membrane, for example, cardiolipins, phosphatidylglycerols, and diacylglycerols. Exogeneous cardiolipin, phosphatidylglycerol, or diacylglycerol antagonized the antibacterial properties of ticagrelor. Ticagrelor enhanced MRSA growth inhibition and killing by vancomycin and daptomycin in both exponential and stationary phases. Finally, no cross-resistance was observed between ticagrelor and daptomycin, or vancomycin. Our study demonstrates that ticagrelor targets multiple lipids in the cytoplasmic membrane of Gram-positive bacteria, thereby retaining activity against multidrug-resistant\n              <jats:italic>staphylococci<\/jats:italic>\n              including daptomycin- and vancomycin-resistant strains.\n            <\/jats:p>\n            <jats:sec>\n              <jats:title>IMPORTANCE<\/jats:title>\n              <jats:p>\n                Infections with multidrug-resistant bacteria pose a major healthcare problem with an urgent need for novel treatment options. The antiplatelet drug ticagrelor possesses antibacterial activity against Gram-positive bacteria including methicillin-resistant and vancomycin-resistant\n                <jats:italic>Staphylococcus aureus<\/jats:italic>\n                strains. We report a unique, dose-dependent, antibacterial mechanism of action of ticagrelor, which alters the properties and integrity of the bacterial cytoplasmic membrane. Ticagrelor retains activity against multidrug-resistant staphylococci, including isolates carrying the most common\n                <jats:italic>in vivo<\/jats:italic>\n                selected daptomycin resistance mutations and vancomycin-intermediate\n                <jats:italic>Staphylococcus aureus<\/jats:italic>\n                . Our data support the use of ticagrelor as adjunct therapy against multidrug-resistant strains. Because of the presence of multiple non-protein targets of this drug within the bacterial membrane, resistance development is expected to be slow. All these findings corroborate the accumulating observational clinical evidence for a beneficial anti-bacterial effect of ticagrelor in cardiovascular patients in need of such treatment.\n              <\/jats:p>\n            <\/jats:sec>\n          <\/jats:sec>","DOI":"10.1128\/mbio.01322-24","type":"journal-article","created":{"date-parts":[[2024,9,27]],"date-time":"2024-09-27T05:18:18Z","timestamp":1727414298000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":10,"title":["Ticagrelor alters the membrane of\n            <i>Staphylococcus aureus<\/i>\n            and enhances the activity of vancomycin and daptomycin without eliciting cross-resistance"],"prefix":"10.1128","volume":"15","author":[{"given":"Kirsten","family":"Leeten","sequence":"first","affiliation":[{"name":"Laboratory of Cardiology, GIGA Research Institute, University of Li\u00e8ge, Li\u00e8ge, Belgium"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nicolas","family":"Jacques","sequence":"additional","affiliation":[{"name":"Laboratory of Cardiology, GIGA Research Institute, University of Li\u00e8ge, Li\u00e8ge, Belgium"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lidia Alejo","family":"Esquembre","sequence":"additional","affiliation":[{"name":"Department of Microbial Bioactive Compounds, Interfaculty Institute of Microbiology and Infection Medicine T\u00fcbingen (IMIT), University of T\u00fcbingen, T\u00fcbingen, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dana C.","family":"Schneider","sequence":"additional","affiliation":[{"name":"Department of Microbial Bioactive Compounds, Interfaculty Institute of Microbiology and Infection Medicine T\u00fcbingen (IMIT), University of T\u00fcbingen, T\u00fcbingen, 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