{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T14:27:28Z","timestamp":1785421648199,"version":"3.56.0"},"reference-count":28,"publisher":"American Society for Microbiology","issue":"3","license":[{"start":{"date-parts":[[2026,3,3]],"date-time":"2026-03-03T00:00:00Z","timestamp":1772496000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,3,3]],"date-time":"2026-03-03T00:00:00Z","timestamp":1772496000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"name":"National Research Foundation of South Africa","award":["115566"],"award-info":[{"award-number":["115566"]}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Microbiol Spectr"],"published-print":{"date-parts":[[2026,3,3]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      Lipids have recently gained attention for their involvement in the virulence of pathogenic yeast. One group of lipids, prostaglandins, which are arachidonic acid-derived eicosanoids, has received particular attention. Prostaglandin E\n                      <jats:sub>2<\/jats:sub>\n                      (PGE\n                      <jats:sub>2<\/jats:sub>\n                      ) is the most studied prostaglandin in mammals. However, pathogenic yeast, including\n                      <jats:italic toggle=\"yes\">Candida albicans<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">Candida tropicalis<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">Candida glabrata<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">Candida parapsilosis<\/jats:italic>\n                      , and\n                      <jats:italic toggle=\"yes\">Candida dubliniensis<\/jats:italic>\n                      , also produces PGE\n                      <jats:sub>2<\/jats:sub>\n                      . Notably, PGE\n                      <jats:sub>2<\/jats:sub>\n                      production has not yet been reported in\n                      <jats:italic toggle=\"yes\">Candidozyma auris<\/jats:italic>\n                      (\n                      <jats:italic toggle=\"yes\">Candida auris<\/jats:italic>\n                      ). In\n                      <jats:italic toggle=\"yes\">C. albicans<\/jats:italic>\n                      , PGE\n                      <jats:sub>2<\/jats:sub>\n                      plays a crucial role in colonization and virulence by promoting yeast-to-hyphal transition, enhancing biofilm formation and colonization of the gastrointestinal tract. Although the biochemical pathway responsible for PGE\n                      <jats:sub>2<\/jats:sub>\n                      synthesis in yeasts is unknown, several genes have been implicated, including\n                      <jats:italic toggle=\"yes\">OLE2<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">POX1-3<\/jats:italic>\n                      , which were investigated in this study. Deletion mutants of these genes were generated using a CRISPR-Cas9 system, and the production of PGE\n                      <jats:sub>2<\/jats:sub>\n                      by the mutants was quantified using enzyme-linked immunosorbent assay and confirmed using liquid chromatography-tandem mass spectrometry. Furthermore, the involvement of these genes in virulence was assessed using a survival assay in\n                      <jats:italic toggle=\"yes\">Caenorhabditis elegans<\/jats:italic>\n                      . This study presents the first report of PGE\n                      <jats:sub>2<\/jats:sub>\n                      production by\n                      <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                      , and it demonstrates that\n                      <jats:italic toggle=\"yes\">OLE2<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">POX1-3<\/jats:italic>\n                      play significant roles in PGE\n                      <jats:sub>2<\/jats:sub>\n                      production and virulence of this yeast in\n                      <jats:italic toggle=\"yes\">C. elegans<\/jats:italic>\n                      . Additionally, deletion of\n                      <jats:italic toggle=\"yes\">OLE2<\/jats:italic>\n                      in\n                      <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                      led to an accumulation of monounsaturated fatty acids, providing evidence that\n                      <jats:italic toggle=\"yes\">OLE2<\/jats:italic>\n                      does not encode a \u03949 desaturase. The conserved nature of the PGE\n                      <jats:sub>2<\/jats:sub>\n                      production and virulence requirements among different pathogenic yeasts indicates the potential for broad-spectrum drug targeting.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>IMPORTANCE<\/jats:title>\n                    <jats:p>\n                      This study reveals, for the first time, that\n                      <jats:italic toggle=\"yes\">Candidozyma<\/jats:italic>\n                      (\n                      <jats:italic toggle=\"yes\">Candida auris<\/jats:italic>\n                      )\u2014a growing global health threat, often causing outbreaks in hospitals\u2014can produce a prostaglandin E\n                      <jats:sub>2<\/jats:sub>\n                      (PGE\n                      <jats:sub>2<\/jats:sub>\n                      ), which is known to influence how the immune system responds and has been linked to increased virulence in other yeast species. By identifying specific genes (\n                      <jats:italic toggle=\"yes\">OLE2<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">POX1-3<\/jats:italic>\n                      ) involved in PGE\n                      <jats:sub>2<\/jats:sub>\n                      production and virulence, potential novel drug targets have been identified. Understanding how\n                      <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                      produces PGE2 and how this contributes to its ability to infect and survive in hosts could lead to innovative therapies that block these pathways, making infections easier to treat.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1128\/spectrum.02323-25","type":"journal-article","created":{"date-parts":[[2026,1,28]],"date-time":"2026-01-28T14:00:14Z","timestamp":1769608814000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["The role of\n                    <i>OLE2<\/i>\n                    and\n                    <i>POX1-3<\/i>\n                    in prostaglandin E\n                    <sub>2<\/sub>\n                    production and virulence is conserved in\n                    <i>Candidozyma<\/i>\n                    (\n                    <i>Candida<\/i>\n  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