{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T15:52:19Z","timestamp":1786117939754,"version":"build-2736575974"},"reference-count":54,"publisher":"American Society for Microbiology","issue":"8","license":[{"start":{"date-parts":[[2026,8,4]],"date-time":"2026-08-04T00:00:00Z","timestamp":1785801600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,8,4]],"date-time":"2026-08-04T00:00:00Z","timestamp":1785801600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"name":"ECDC Fellowship Programme"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Microbiol Spectr"],"published-print":{"date-parts":[[2026,8,4]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      <jats:italic toggle=\"yes\">Candidozyma auris<\/jats:italic>\n                      (formerly\n                      <jats:italic toggle=\"yes\">Candida auris<\/jats:italic>\n                      ) has emerged as a critical nosocomial pathogen, notable for its multidrug resistance and its capability to form biofilms that enable persistence on surfaces. Although effective disinfection strategies are urgently needed, current disinfectant efficacy standards in many regions, such as Europe, are primarily based on testing planktonic\n                      <jats:italic toggle=\"yes\">Candida albicans<\/jats:italic>\n                      and do not adequately reflect the resilience of\n                      <jats:italic toggle=\"yes\">Candida<\/jats:italic>\n                      biofilms, including those of\n                      <jats:italic toggle=\"yes\">C. albicans<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                      . To address this gap, the Bead Assay for Biofilms, previously developed for bacterial biofilms, was adapted for the first time to eukaryotic cells. The goal was to cultivate\n                      <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">C. albicans<\/jats:italic>\n                      biofilms and evaluate the efficacy of selected disinfectants across four active substance classes. Cell enumeration demonstrated highly reproducible biofilms, whose architecture was confirmed by scanning electron microscopy. Both an alcohol- and a QAC-based product did not achieve sufficient reduction of at least \u22654 log\n                      <jats:sub>10<\/jats:sub>\n                      CFU\/mL of biofilm-cells when applied under conditions recommended by the manufacturer (alcohol 1 min:\n                      <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                      0.82,\n                      <jats:italic toggle=\"yes\">C. albicans<\/jats:italic>\n                      0.54; QAC 1%, 15 min:\n                      <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                      1.94,\n                      <jats:italic toggle=\"yes\">C. albicans<\/jats:italic>\n                      0.68). This reduced efficacy is consistent with the known increased tolerance of microorganisms in biofilms. In contrast, peracetic acid and glutaraldehyde achieved sufficient reductions, albeit at relatively high concentrations (peracetic acid 0.1%:\n                      <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                      4.75 and 0.05%:\n                      <jats:italic toggle=\"yes\">C. albicans<\/jats:italic>\n                      4.87; glutaraldehyde 0.5%:\n                      <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                      5.32 and\n                      <jats:italic toggle=\"yes\">C. albicans<\/jats:italic>\n                      4.15). Our findings underscore the need to adapt disinfection protocols and testing models to consider biofilm formation of\n                      <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">C. albicans<\/jats:italic>\n                      , and species-specific resilience.\n                    <\/jats:p>\n                    <jats:sec>\n                      <jats:title>IMPORTANCE<\/jats:title>\n                      <jats:p>\n                        This study highlights a critical gap in current disinfection efficacy testing standards; many of which rely on planktonic cell models and do not account for the resilience of biofilm-associated cells or emerging pathogens with unique resistance traits. Although species-specific regulatory guidance for\n                        <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                        exists in certain regions (e.g., in the USA), standardized disinfectant testing remains largely based on suspension assays (often using\n                        <jats:italic toggle=\"yes\">C. albicans<\/jats:italic>\n                        ) and does not routinely incorporate biofilm models. Using the Bead Assay for Biofilms, we demonstrate that several commonly used disinfectants may fail to inactivate biofilm-associated\n                        <jats:italic toggle=\"yes\">C. auris<\/jats:italic>\n                        and\n                        <jats:italic toggle=\"yes\">C. albicans<\/jats:italic>\n                        when applied as recommended. This suggests that reliance on planktonic testing may overestimate disinfectant efficacy against clinically relevant pathogenic yeast and highlights the need to expand current testing standards in order to include biofilm-associated pathogens to improve infection prevention strategies. Consequently, our research is of immediate relevance to regulatory bodies, infection control, and public health.\n                      <\/jats:p>\n                    <\/jats:sec>\n                  <\/jats:sec>","DOI":"10.1128\/spectrum.03582-25","type":"journal-article","created":{"date-parts":[[2026,7,2]],"date-time":"2026-07-02T15:41:13Z","timestamp":1783006873000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["Disinfectant tolerance of\n                    <i>Candidozyma auris<\/i>\n                    and\n                    <i>Candida albicans<\/i>\n                    biofilms evaluated using the bead assay for biofilms"],"prefix":"10.1128","volume":"14","author":[{"given":"Natalia M.","family":"Zmarlak-Feher","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01k5qnb77","id-type":"ROR","asserted-by":"publisher"}],"name":"Mycotic and Parasitic Agents and Mycobacteria, Department of Infectious Diseases, Robert Koch Institute","place":["Berlin, Germany"]},{"id":[{"id":"https:\/\/ror.org\/00s9v1h75","id-type":"ROR","asserted-by":"publisher"}],"name":"ECDC Fellowship Programme, Public Health Microbiology Path (EUPHEM), European Centre for Disease Prevention and Control (ECDC)","place":["Stockholm, Sweden"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Antje","family":"Finke","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01k5qnb77","id-type":"ROR","asserted-by":"publisher"}],"name":"Hospital Hygiene, Infection Prevention and Control, Department of Infectious Diseases, Robert Koch Institute","place":["Berlin, Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katharina","family":"Konrat","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01k5qnb77","id-type":"ROR","asserted-by":"publisher"}],"name":"Hospital Hygiene, Infection Prevention and Control, Department of Infectious Diseases, Robert Koch Institute","place":["Berlin, Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christoph","family":"Schaudinn","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01k5qnb77","id-type":"ROR","asserted-by":"publisher"}],"name":"Advanced Light and Electron Microscopy, Robert Koch Institute","place":["Berlin, Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mardjan","family":"Arvand","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01k5qnb77","id-type":"ROR","asserted-by":"publisher"}],"name":"Hospital Hygiene, Infection Prevention and Control, Department of Infectious Diseases, Robert Koch Institute","place":["Berlin, Germany"]},{"name":"Department of Infectious Diseases, Institute for Medical Microbiology and Hygiene, University of Heidelberg","place":["Heidelberg, Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5297-3750","authenticated-orcid":true,"given":"Anja M.","family":"Richter","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01k5qnb77","id-type":"ROR","asserted-by":"publisher"}],"name":"Hospital Hygiene, Infection Prevention and Control, Department of Infectious Diseases, Robert Koch Institute","place":["Berlin, Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"235","reference":[{"key":"e_1_3_2_2_2","doi-asserted-by":"publisher","DOI":"10.1016\/S1473-3099(10)70218-8"},{"key":"e_1_3_2_3_2","doi-asserted-by":"publisher","DOI":"10.3767\/persoonia.2024.52.02"},{"key":"e_1_3_2_4_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1348-0421.2008.00083.x"},{"key":"e_1_3_2_5_2","unstructured":"About C. auris. 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