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ALS3 Expression as an Indicator for Candida albicans Biofilm Formation and Drug Resistance

Resistance caused by the formation of the Candida albicans (C. albicans) biofilm is one of the main reasons for antifungal therapy failure. Thus, it is important to find indicators that predict C. albicans biofilm formation to provide evidence for the early prevention and treatment of the C. albican...

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Autores principales: Deng, Keke, Jiang, Wei, Jiang, Yanyu, Deng, Qi, Cao, Jinzhong, Yang, Wenjie, Zhao, Xuequn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117015/
https://www.ncbi.nlm.nih.gov/pubmed/33995316
http://dx.doi.org/10.3389/fmicb.2021.655242
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author Deng, Keke
Jiang, Wei
Jiang, Yanyu
Deng, Qi
Cao, Jinzhong
Yang, Wenjie
Zhao, Xuequn
author_facet Deng, Keke
Jiang, Wei
Jiang, Yanyu
Deng, Qi
Cao, Jinzhong
Yang, Wenjie
Zhao, Xuequn
author_sort Deng, Keke
collection PubMed
description Resistance caused by the formation of the Candida albicans (C. albicans) biofilm is one of the main reasons for antifungal therapy failure. Thus, it is important to find indicators that predict C. albicans biofilm formation to provide evidence for the early prevention and treatment of the C. albicans biofilms. In this study, C. albicans samples were selected from C. albicans septicemia that were sensitive to common antifungal agents. It was found that the agglutinin-like sequence 3 (ALS3) gene was differentially expressed in free, antifungal, drug-sensitive C. albicans. The average ALS3 gene expression was higher in the C. albicans strains with biofilm formation than that in the C. albicans strains without biofilm formation. Then, it was further confirmed that the rate of biofilm formation was higher in the high ALS3 gene expression group than that in the low ALS3 gene expression group. It was found that C. albicans with biofilm formation was more resistant to fluconazole, voriconazole, and itraconazole. However, it maintained its sensitivity to caspofungin and micafungin in vitro and in mice. Further experiments regarding the prevention of C. albicans biofilm formation were performed in mice, in which only caspofungin and micafungin prevented C. albicans biofilm formation. These results suggest that the expression level of ALS3 in C. albicans may be used as an indicator to determine whether C. albicans will form biofilms. The results also show that the biofilm formation of C. albicans remained sensitive to caspofungin and micafungin, which may help to guide the selection of clinical antifungal agents for prevention and therapy.
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spelling pubmed-81170152021-05-14 ALS3 Expression as an Indicator for Candida albicans Biofilm Formation and Drug Resistance Deng, Keke Jiang, Wei Jiang, Yanyu Deng, Qi Cao, Jinzhong Yang, Wenjie Zhao, Xuequn Front Microbiol Microbiology Resistance caused by the formation of the Candida albicans (C. albicans) biofilm is one of the main reasons for antifungal therapy failure. Thus, it is important to find indicators that predict C. albicans biofilm formation to provide evidence for the early prevention and treatment of the C. albicans biofilms. In this study, C. albicans samples were selected from C. albicans septicemia that were sensitive to common antifungal agents. It was found that the agglutinin-like sequence 3 (ALS3) gene was differentially expressed in free, antifungal, drug-sensitive C. albicans. The average ALS3 gene expression was higher in the C. albicans strains with biofilm formation than that in the C. albicans strains without biofilm formation. Then, it was further confirmed that the rate of biofilm formation was higher in the high ALS3 gene expression group than that in the low ALS3 gene expression group. It was found that C. albicans with biofilm formation was more resistant to fluconazole, voriconazole, and itraconazole. However, it maintained its sensitivity to caspofungin and micafungin in vitro and in mice. Further experiments regarding the prevention of C. albicans biofilm formation were performed in mice, in which only caspofungin and micafungin prevented C. albicans biofilm formation. These results suggest that the expression level of ALS3 in C. albicans may be used as an indicator to determine whether C. albicans will form biofilms. The results also show that the biofilm formation of C. albicans remained sensitive to caspofungin and micafungin, which may help to guide the selection of clinical antifungal agents for prevention and therapy. Frontiers Media S.A. 2021-04-29 /pmc/articles/PMC8117015/ /pubmed/33995316 http://dx.doi.org/10.3389/fmicb.2021.655242 Text en Copyright © 2021 Deng, Jiang, Jiang, Deng, Cao, Yang and Zhao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Deng, Keke
Jiang, Wei
Jiang, Yanyu
Deng, Qi
Cao, Jinzhong
Yang, Wenjie
Zhao, Xuequn
ALS3 Expression as an Indicator for Candida albicans Biofilm Formation and Drug Resistance
title ALS3 Expression as an Indicator for Candida albicans Biofilm Formation and Drug Resistance
title_full ALS3 Expression as an Indicator for Candida albicans Biofilm Formation and Drug Resistance
title_fullStr ALS3 Expression as an Indicator for Candida albicans Biofilm Formation and Drug Resistance
title_full_unstemmed ALS3 Expression as an Indicator for Candida albicans Biofilm Formation and Drug Resistance
title_short ALS3 Expression as an Indicator for Candida albicans Biofilm Formation and Drug Resistance
title_sort als3 expression as an indicator for candida albicans biofilm formation and drug resistance
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117015/
https://www.ncbi.nlm.nih.gov/pubmed/33995316
http://dx.doi.org/10.3389/fmicb.2021.655242
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