{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T16:24:00Z","timestamp":1791390240093,"version":"4.3.3"},"reference-count":53,"publisher":"American Society for Microbiology","issue":"1","license":[{"start":{"date-parts":[[2013,1,1]],"date-time":"2013-01-01T00:00:00Z","timestamp":1356998400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Antimicrob Agents Chemother"],"published-print":{"date-parts":[[2013,1]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:p>\n            The objective of this study was to evaluate whether\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Candida albicans<\/jats:named-content>\n            exhibits altered pathogenicity characteristics following sublethal antimicrobial photodynamic inactivation (APDI) and if such alterations are maintained in the daughter cells.\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">C. albicans<\/jats:named-content>\n            was exposed to sublethal APDI by using methylene blue (MB) as a photosensitizer (0.05 mM) combined with a GaAlAs diode laser (\u03bb 660 nm, 75 mW\/cm\n            <jats:sup>2<\/jats:sup>\n            , 9 to 27 J\/cm\n            <jats:sup>2<\/jats:sup>\n            ).\n            <jats:italic>In vitro<\/jats:italic>\n            , we evaluated APDI effects on\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">C. albicans<\/jats:named-content>\n            growth, germ tube formation, sensitivity to oxidative and osmotic stress, cell wall integrity, and fluconazole susceptibility.\n            <jats:italic>In vivo<\/jats:italic>\n            , we evaluated\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">C. albicans<\/jats:named-content>\n            pathogenicity with a mouse model of systemic infection. Animal survival was evaluated daily. Sublethal MB-mediated APDI reduced the growth rate and the ability of\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">C. albicans<\/jats:named-content>\n            to form germ tubes compared to untreated cells (\n            <jats:italic>P<\/jats:italic>\n            &lt; 0.05). Survival of mice systemically infected with\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">C. albicans<\/jats:named-content>\n            pretreated with APDI was significantly increased compared to mice infected with untreated yeast (\n            <jats:italic>P<\/jats:italic>\n            &lt; 0.05). APDI increased\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">C. albicans<\/jats:named-content>\n            sensitivity to sodium dodecyl sulfate, caffeine, and hydrogen peroxide. The MIC for fluconazole for\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">C. albicans<\/jats:named-content>\n            was also reduced following sublethal MB-mediated APDI. However, none of those pathogenic parameters was altered in daughter cells of\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">C. albicans<\/jats:named-content>\n            submitted to APDI. These data suggest that APDI may inhibit virulence factors and reduce\n            <jats:italic>in vivo<\/jats:italic>\n            pathogenicity of\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">C. albicans<\/jats:named-content>\n            . The absence of alterations in daughter cells indicates that APDI effects are transitory. The MIC reduction for fluconazole following APDI suggests that this antifungal could be combined with APDI to treat\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">C. albicans<\/jats:named-content>\n            infections.\n          <\/jats:p>","DOI":"10.1128\/aac.01451-12","type":"journal-article","created":{"date-parts":[[2012,11,6]],"date-time":"2012-11-06T00:32:19Z","timestamp":1352161939000},"page":"445-451","update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":77,"title":["Antimicrobial Photodynamic Inactivation Inhibits Candida albicans Virulence Factors and Reduces\n            <i>In Vivo<\/i>\n            Pathogenicity"],"prefix":"10.1128","volume":"57","author":[{"given":"Ilka Tiemy","family":"Kato","sequence":"first","affiliation":[{"name":"Center for Lasers and Applications, IPEN-CNEN\/SP, S\u00e3o Paulo, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Renato Araujo","family":"Prates","sequence":"additional","affiliation":[{"name":"Center for Lasers and Applications, IPEN-CNEN\/SP, S\u00e3o Paulo, Brazil"},{"name":"Dentistry School, Health Division and Biophotonics Program of UNINOVE, S\u00e3o Paulo, S\u00e3o Paulo, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Caetano Padial","family":"Sabino","sequence":"additional","affiliation":[{"name":"Center for Lasers and Applications, IPEN-CNEN\/SP, S\u00e3o Paulo, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Beth Burgwyn","family":"Fuchs","sequence":"additional","affiliation":[{"name":"Harvard Medical School, Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"George P.","family":"Tegos","sequence":"additional","affiliation":[{"name":"Department of Pathology, School of Medicine, and Center for Molecular Discovery, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA"},{"name":"Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA"},{"name":"Department of Dermatology, Harvard Medical School, Boston, Massachusetts, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eleftherios","family":"Mylonakis","sequence":"additional","affiliation":[{"name":"Harvard Medical School, Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael R.","family":"Hamblin","sequence":"additional","affiliation":[{"name":"Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA"},{"name":"Department of Dermatology, Harvard Medical School, Boston, Massachusetts, USA"},{"name":"Harvard\u2014MIT Division of Health Sciences and Technology, Cambridge, 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