{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,11]],"date-time":"2026-10-11T13:45:07Z","timestamp":1791726307931,"version":"4.3.4"},"reference-count":47,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2025,5,6]],"date-time":"2025-05-06T00:00:00Z","timestamp":1746489600000},"content-version":"vor","delay-in-days":5,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2025,5,1]],"date-time":"2025-05-01T00:00:00Z","timestamp":1746057600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/501100001411","name":"Indian Council of Medical Research","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100001411","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Mycoses"],"published-print":{"date-parts":[[2025,5]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      The recent rise in the global incidence of fluconazole resistance in\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>C. parapsilosis<\/jats:italic>\n                      <\/jats:styled-content>\n                      has become a significant public health concern. Epidemiological studies suggest that fluconazole resistance in\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>C. parapsilosis<\/jats:italic>\n                      <\/jats:styled-content>\n                      spreads through endemic clones. We, therefore, investigated the molecular epidemiology of fluconazole\u2010resistant\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>C. parapsilosis<\/jats:italic>\n                      <\/jats:styled-content>\n                      in our centre.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>C. parapsilosis<\/jats:italic>\n                      <\/jats:styled-content>\n                      isolates from 2016 through 2022 were investigated for antifungal susceptibility. Fluconazole\u2010resistant isolates were analysed for\n                      <jats:italic>ERG<\/jats:italic>\n                      11 mutation using Sanger sequencing. Gene expression profiles of\n                      <jats:italic>ERG<\/jats:italic>\n                      11,\n                      <jats:italic>CDR<\/jats:italic>\n                      1 and\n                      <jats:italic>MDR<\/jats:italic>\n                      1 were assessed by real\u2010time qPCR. The epidemiological relationship of resistant and susceptible isolates of\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>C. parapsilosis<\/jats:italic>\n                      <\/jats:styled-content>\n                      was investigated using short tandem repeat typing. Additionally, biofilm production and cell wall ergosterol contents were also quantified and compared.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Among 572\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>C. parapsilosis<\/jats:italic>\n                      <\/jats:styled-content>\n                      isolates, 48 (8.4%) were resistant to fluconazole. Of 28 recoverable resistant isolates, 17.9% (5\/28) were wild\u2010type and 82.1% (23\/28) harboured the following\n                      <jats:italic>ERG<\/jats:italic>\n                      11 mutations: Y132F (\n                      <jats:italic>n<\/jats:italic>\n                      =\u20093), K143R (\n                      <jats:italic>n<\/jats:italic>\n                      =\u200910) and K143R + R398I (10\/28). Significant fold\u2010changes were observed in\n                      <jats:italic>ERG<\/jats:italic>\n                      11 (\n                      <jats:italic>p<\/jats:italic>\n                      =\u20090.037) and\n                      <jats:italic>MDR<\/jats:italic>\n                      1 (\n                      <jats:italic>p<\/jats:italic>\n                      =\u20090.008) gene expressions in fluconazole resistant compared to susceptible isolates. Contrary to global reports, STR typing suggested a limited clonal transmission of resistant\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>C. parapsilosis<\/jats:italic>\n                      <\/jats:styled-content>\n                      with multiple introductions of resistant isolates in our centre. On fluconazole exposure, ergosterol content significantly increased (\n                      <jats:italic>p<\/jats:italic>\n                      &lt;\u20090.01) in resistant isolates, particularly in isolates harbouring\n                      <jats:italic>ERG<\/jats:italic>\n                      11\n                      <jats:sup>K143R + R398I<\/jats:sup>\n                      mutations. In contrast, fluconazole\u2010susceptible isolates formed comparatively higher baseline biofilm (\n                      <jats:italic>p<\/jats:italic>\n                      &lt;\u20090.05) than resistant isolates with\n                      <jats:italic>ERG<\/jats:italic>\n                      11\n                      <jats:sup>K143R<\/jats:sup>\n                      mutation.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      The current study underscores the need for continuous molecular surveillance and tailored therapeutic options for effective management of fluconazole resistance in\n                      <jats:styled-content style=\"fixed-case\">\n                        <jats:italic>C. parapsilosis<\/jats:italic>\n                      <\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/myc.70062","type":"journal-article","created":{"date-parts":[[2025,5,6]],"date-time":"2025-05-06T06:58:48Z","timestamp":1746514728000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Genotypic Diversity and Molecular Basis of Fluconazole Resistance in\n                    <scp>\n                      <i>Candida parapsilosis<\/i>\n                    <\/scp>\n                    Clinical Isolates Collected Over 7\u2009Years in a Tertiary\u2010Care Hospital in North India"],"prefix":"10.1111","volume":"68","author":[{"given":"Vrinda","family":"Sharma","sequence":"first","affiliation":[{"name":"Department of Medical Microbiology Postgraduate Institute of Medical Education &amp; 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