{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T03:18:55Z","timestamp":1787800735781,"version":"build-2784847793"},"reference-count":70,"publisher":"American Association for the Advancement of Science (AAAS)","issue":"8","content-domain":{"domain":["www.science.org"],"crossmark-restriction":true},"short-container-title":["Sci. Adv."],"published-print":{"date-parts":[[2023,2,24]]},"abstract":"<jats:p>\n                    Antibiotic resistance critically limits treatment options for infection caused by opportunistic pathogens such as enterococci. Here, we investigate the antibiotic and immunological activity of the anticancer agent mitoxantrone (MTX) in vitro and in vivo against vancomycin-resistant\n                    <jats:italic>Enterococcus faecalis<\/jats:italic>\n                    (VRE). We show that, in vitro, MTX is a potent antibiotic against Gram-positive bacteria through induction of reactive oxygen species and DNA damage. MTX also synergizes with vancomycin against VRE, rendering the resistant strains more permeable to MTX. In a murine wound infection model, single-dose MTX treatment effectively reduces VRE numbers, with further reduction when combined with vancomycin. Multiple MTX treatments accelerate wound closure. MTX also promotes macrophage recruitment and proinflammatory cytokine induction at the wound site and augments intracellular bacterial killing in macrophages by up-regulating the expression of lysosomal enzymes. These results show that MTX represents a promising bacterium- and host-targeted therapeutic for overcoming vancomycin resistance.\n                  <\/jats:p>","DOI":"10.1126\/sciadv.add9280","type":"journal-article","created":{"date-parts":[[2023,2,22]],"date-time":"2023-02-22T13:57:21Z","timestamp":1677074241000},"update-policy":"https:\/\/doi.org\/10.34133\/aaas_crossmark","source":"Crossref","is-referenced-by-count":36,"title":["Mitoxantrone targets both host and bacteria to overcome vancomycin resistance in\n                    <i>Enterococcus faecalis<\/i>"],"prefix":"10.1126","volume":"9","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-8879-6407","authenticated-orcid":true,"given":"Ronni A.\u00a0G.","family":"da Silva","sequence":"first","affiliation":[{"name":"Singapore-MIT Alliance for Research and Technology, Antimicrobial Drug Resistance Interdisciplinary Research Group, Singapore, Singapore."},{"name":"Singapore Centre for Environmental Life Sciences Engineering, 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