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These infections are typically investigated using the\n                    <jats:styled-content style=\"fixed-case\">\n                      <jats:italic>C. albicans<\/jats:italic>\n                    <\/jats:styled-content>\n                    strain SC5314, despite its uncertain clinical relevance. Here, we evaluate how different\n                    <jats:styled-content style=\"fixed-case\">\n                      <jats:italic>C. albicans<\/jats:italic>\n                    <\/jats:styled-content>\n                    (high, intermediate, low biofilm formers) and\n                    <jats:styled-content style=\"fixed-case\">\n                      <jats:italic>S. aureus<\/jats:italic>\n                    <\/jats:styled-content>\n                    strains influence biofilm tolerance to both conventional antimicrobials and cold atmospheric plasma (CAP). CAP is an emerging technology that has been shown, including in our prior work, to disrupt biofilm biomass via reactive oxygen and nitrogen species, positioning it as a promising adjunct to antimicrobial therapy. We determined how strain variation influenced biofilm structure and tolerance to vancomycin, amphotericin B and CAP. Interkingdom biofilm architecture was primarily influenced by the\n                    <jats:styled-content style=\"fixed-case\">\n                      <jats:italic>C. albicans<\/jats:italic>\n                    <\/jats:styled-content>\n                    strain, particularly its ability to form hyphae. Despite this, all strains conferred protection to\n                    <jats:styled-content style=\"fixed-case\">\n                      <jats:italic>S. aureus<\/jats:italic>\n                    <\/jats:styled-content>\n                    against vancomycin. CAP eradicated\n                    <jats:styled-content style=\"fixed-case\">\n                      <jats:italic>S. aureus<\/jats:italic>\n                    <\/jats:styled-content>\n                    biofilms within 120\u2009s, but this effect was lost in dual\u2010species biofilms. However, CAP pretreatment enhanced the efficacy of both antimicrobials in interkingdom biofilms. These findings highlight the role of hyphal morphology in vancomycin tolerance and support further clinical evaluation of CAP as a biofilm\u2010targeting adjunct.\n                  <\/jats:p>","DOI":"10.1111\/apm.70119","type":"journal-article","created":{"date-parts":[[2025,12,29]],"date-time":"2025-12-29T08:32:01Z","timestamp":1766997121000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Understanding Heterogeneity and Tolerance of Dual\n                    <scp>\n                      <i>Candida albicans\u2013Staphylococcus aureus<\/i>\n                    <\/scp>\n                    Biofilms to Cold Atmospheric Plasma and Antimicrobial Combinations"],"prefix":"10.1111","volume":"133","author":[{"given":"Ross M.","family":"Duncan","sequence":"first","affiliation":[{"name":"School of Pharmacy Queen's University Belfast  Belfast UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thomas 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