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Given the limited therapeutic arsenal, drug repurposing represents a promising strategy for antifungal discovery. This study evaluated the antifungal activity and mechanisms of auranofin and iodoquinol against filamentous fungi listed as World Health Organization (WHO) priority pathogens, including\n                      <jats:italic toggle=\"yes\">Aspergillus fumigatus<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">Fusarium oxysporum<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">Scedosporium boydii<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">Lomentospora prolificans<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">Rhizopus oryzae<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">Mucor velutinosus<\/jats:italic>\n                      , and\n                      <jats:italic toggle=\"yes\">Cunninghamella<\/jats:italic>\n                      sp. Although\n                      <jats:italic toggle=\"yes\">Aspergillus flavus<\/jats:italic>\n                      is not included in the WHO priority list, it was included in this study due to its clinical relevance as a major cause of aspergillosis and fungal rhinosinusitis. Auranofin displayed fungicidal activity against\n                      <jats:italic toggle=\"yes\">Aspergillus<\/jats:italic>\n                      spp.,\n                      <jats:italic toggle=\"yes\">L. prolificans<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">S. boydii<\/jats:italic>\n                      , and\n                      <jats:italic toggle=\"yes\">R. oryzae<\/jats:italic>\n                      , while iodoquinol exhibited potent but mainly fungistatic effects, with minimum inhibitory concentration values ranging from 0.625 to 20 \u00b5M. Both compounds inhibited early growth and reduced preformed biofilms by over 50% in biomass and metabolic activity. Stress susceptibility and fluorescence assays indicated that auranofin interferes with lipid homeostasis, cell wall integrity, and oxidative stress responses, whereas iodoquinol alters membrane lipids, mannose, and chitin distribution, suggesting multitarget surface effects. Scanning electron microscopy revealed consistent ultrastructural alterations, including hyphal deformation and increased extracellular matrix deposition in\n                      <jats:italic toggle=\"yes\">A. fumigatus<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">F. oxysporum<\/jats:italic>\n                      treated with sub-inhibitory drug concentrations, corroborating the observed cellular stress responses. Drug interaction assays demonstrated additive or synergistic effects with voriconazole and amphotericin B, but not with posaconazole. Overall, auranofin and iodoquinol exhibit broad-spectrum antifungal activity, disrupt fungal morphology and physiology, and represent promising repurposed candidates for developing novel combination therapies against refractory mycoses.\n                    <\/jats:p>\n                    <jats:sec>\n                      <jats:title>IMPORTANCE<\/jats:title>\n                      <jats:p>\n                        Mycoses caused by opportunistic fungi are an increasingly public health problem, particularly in immunocompromised individuals, due to their high virulence and resistance to conventional antifungals. The World Health Organization\u2019s priority fungal pathogens list points out a variety of filamentous fungi, such as\n                        <jats:italic toggle=\"yes\">Aspergillus fumigatus<\/jats:italic>\n                        ,\n                        <jats:italic toggle=\"yes\">A. flavus<\/jats:italic>\n                        ,\n                        <jats:italic toggle=\"yes\">Fusarium oxysporum<\/jats:italic>\n                        ,\n                        <jats:italic toggle=\"yes\">Scedosporium boydii<\/jats:italic>\n                        ,\n                        <jats:italic toggle=\"yes\">Lomentospora prolificans<\/jats:italic>\n                        ,\n                        <jats:italic toggle=\"yes\">Rhizopus oryzae<\/jats:italic>\n                        ,\n                        <jats:italic toggle=\"yes\">Mucor velutinosus<\/jats:italic>\n                        , and\n                        <jats:italic toggle=\"yes\">Cunninghamella<\/jats:italic>\n                        sp. Given the limited therapeutic arsenal to combat them, drug repurposing represents a promising strategy for antifungal discovery. The present study evaluated the antifungal activity and some cellular alterations caused by auranofin and iodoquinol, which are already available in clinical settings to treat rheumatoid arthritis and infections by amoeba, respectively. The data presented in the study revealed that both drugs display a wide spectrum of action against different fungal pathogens, as well as contribute to highlight the potential of them as repurposing drugs to be investigated as alternatives for the treatment of mycoses.\n                      <\/jats:p>\n                    <\/jats:sec>\n                  <\/jats:sec>","DOI":"10.1128\/spectrum.03356-25","type":"journal-article","created":{"date-parts":[[2026,2,27]],"date-time":"2026-02-27T14:00:42Z","timestamp":1772200842000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["Auranofin and iodoquinol as promising repurposing drugs against filamentous fungi: antifungal activity and cellular alterations"],"prefix":"10.1128","volume":"14","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1803-6381","authenticated-orcid":false,"given":"Mariana Ingrid Dutra da 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