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Identification and susceptibility testing of oral candidiasis in advanced cancer patients
BACKGROUND: Patients with advanced cancer are prone to develop different opportunistic oral infection due to anti-cancer treatment or the malignancies themselves. Studies of oral fungal samples show an increased prevalence of non-Candida albicans species in mixed oral infections with Candida albican...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10111683/ https://www.ncbi.nlm.nih.gov/pubmed/37072843 http://dx.doi.org/10.1186/s12903-023-02950-y |
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author | Monsen, Ragnhild Elisabeth Kristoffersen, Anne Karin Gay, Caryl L. Herlofson, Bente Brokstad Fjeld, Katrine Gahre Hove, Lene Hystad Nordgarden, Hilde Tollisen, Anita Lerdal, Anners Enersen, Morten |
author_facet | Monsen, Ragnhild Elisabeth Kristoffersen, Anne Karin Gay, Caryl L. Herlofson, Bente Brokstad Fjeld, Katrine Gahre Hove, Lene Hystad Nordgarden, Hilde Tollisen, Anita Lerdal, Anners Enersen, Morten |
author_sort | Monsen, Ragnhild Elisabeth |
collection | PubMed |
description | BACKGROUND: Patients with advanced cancer are prone to develop different opportunistic oral infection due to anti-cancer treatment or the malignancies themselves. Studies of oral fungal samples show an increased prevalence of non-Candida albicans species in mixed oral infections with Candida albicans. Non-C. albicans and C. albicans are associated with varying degrees of resistance to azoles, which may have implications for treatment. This study aimed to assess the diversity and antifungal susceptibility of Candida species detected in the oral cavity. METHODS: An observational study with microbiological analysis was conducted. Clinical fungal isolates were collected from patients in a hospice unit in 2014–2016. Isolates were re-grown on chromID® Candida plates in 2020. Single colony of each species was re-cultivated and prepared for biochemical identification with a VITEK2® system and verified by gene sequencing. Etest was performed on RPMI agar, and the antifungals fluconazole, amphotericin B, anidulafungin and nystatin were applied. RESULTS: Fifty-six isolates from 45 patients were identified. Seven different Candida species and one Saccharomyces species were detected. The results of biochemical identification were confirmed with sequencing analysis. Thirty-six patients had mono infection, and nine out of 45 patients had 2–3 different species detected. Of C. albicans strains, 39 out of 40 were susceptible to fluconazole. Two non-C. albicans species were resistant to fluconazole, one to amphotericin B and three to anidulafungin. CONCLUSION: C. albicans was the predominant species, with a high susceptibility to antifungal agents. Different Candida species occur in both mono and mixed infections. Identification and susceptibility testing may therefore lead to more effective treatment and may prevent the development of resistance among patients with advanced cancer. TRAIL REGISTRATION: The study Oral Health in Advanced Cancer was registered at ClinicalTrials.gov (#NCT02067572) in 20/02/2014. |
format | Online Article Text |
id | pubmed-10111683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101116832023-04-19 Identification and susceptibility testing of oral candidiasis in advanced cancer patients Monsen, Ragnhild Elisabeth Kristoffersen, Anne Karin Gay, Caryl L. Herlofson, Bente Brokstad Fjeld, Katrine Gahre Hove, Lene Hystad Nordgarden, Hilde Tollisen, Anita Lerdal, Anners Enersen, Morten BMC Oral Health Research BACKGROUND: Patients with advanced cancer are prone to develop different opportunistic oral infection due to anti-cancer treatment or the malignancies themselves. Studies of oral fungal samples show an increased prevalence of non-Candida albicans species in mixed oral infections with Candida albicans. Non-C. albicans and C. albicans are associated with varying degrees of resistance to azoles, which may have implications for treatment. This study aimed to assess the diversity and antifungal susceptibility of Candida species detected in the oral cavity. METHODS: An observational study with microbiological analysis was conducted. Clinical fungal isolates were collected from patients in a hospice unit in 2014–2016. Isolates were re-grown on chromID® Candida plates in 2020. Single colony of each species was re-cultivated and prepared for biochemical identification with a VITEK2® system and verified by gene sequencing. Etest was performed on RPMI agar, and the antifungals fluconazole, amphotericin B, anidulafungin and nystatin were applied. RESULTS: Fifty-six isolates from 45 patients were identified. Seven different Candida species and one Saccharomyces species were detected. The results of biochemical identification were confirmed with sequencing analysis. Thirty-six patients had mono infection, and nine out of 45 patients had 2–3 different species detected. Of C. albicans strains, 39 out of 40 were susceptible to fluconazole. Two non-C. albicans species were resistant to fluconazole, one to amphotericin B and three to anidulafungin. CONCLUSION: C. albicans was the predominant species, with a high susceptibility to antifungal agents. Different Candida species occur in both mono and mixed infections. Identification and susceptibility testing may therefore lead to more effective treatment and may prevent the development of resistance among patients with advanced cancer. TRAIL REGISTRATION: The study Oral Health in Advanced Cancer was registered at ClinicalTrials.gov (#NCT02067572) in 20/02/2014. BioMed Central 2023-04-18 /pmc/articles/PMC10111683/ /pubmed/37072843 http://dx.doi.org/10.1186/s12903-023-02950-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Monsen, Ragnhild Elisabeth Kristoffersen, Anne Karin Gay, Caryl L. Herlofson, Bente Brokstad Fjeld, Katrine Gahre Hove, Lene Hystad Nordgarden, Hilde Tollisen, Anita Lerdal, Anners Enersen, Morten Identification and susceptibility testing of oral candidiasis in advanced cancer patients |
title | Identification and susceptibility testing of oral candidiasis in advanced cancer patients |
title_full | Identification and susceptibility testing of oral candidiasis in advanced cancer patients |
title_fullStr | Identification and susceptibility testing of oral candidiasis in advanced cancer patients |
title_full_unstemmed | Identification and susceptibility testing of oral candidiasis in advanced cancer patients |
title_short | Identification and susceptibility testing of oral candidiasis in advanced cancer patients |
title_sort | identification and susceptibility testing of oral candidiasis in advanced cancer patients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10111683/ https://www.ncbi.nlm.nih.gov/pubmed/37072843 http://dx.doi.org/10.1186/s12903-023-02950-y |
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