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Quantitative assay for farnesol and the aromatic fusel alcohols from the fungus Candida albicans

ABSTRACT: The dimorphic fungus Candida albicans is a commensal and opportunistic fungal pathogen of humans. It secretes at least four small lipophilic molecules, farnesol and three aromatic fusel alcohols. Farnesol has been identified as both a quorum sensing molecule (QSM) and a virulence factor. O...

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Autores principales: Boone, Cory H. T., Gutzmann, Daniel J., Kramer, Jaxon J., Atkin, Audrey L., Nickerson, Kenneth W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529689/
https://www.ncbi.nlm.nih.gov/pubmed/36107213
http://dx.doi.org/10.1007/s00253-022-12165-w
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author Boone, Cory H. T.
Gutzmann, Daniel J.
Kramer, Jaxon J.
Atkin, Audrey L.
Nickerson, Kenneth W.
author_facet Boone, Cory H. T.
Gutzmann, Daniel J.
Kramer, Jaxon J.
Atkin, Audrey L.
Nickerson, Kenneth W.
author_sort Boone, Cory H. T.
collection PubMed
description ABSTRACT: The dimorphic fungus Candida albicans is a commensal and opportunistic fungal pathogen of humans. It secretes at least four small lipophilic molecules, farnesol and three aromatic fusel alcohols. Farnesol has been identified as both a quorum sensing molecule (QSM) and a virulence factor. Our gas chromatography (GC)-based assay for these molecules exhibits high throughput, prevention of analyte loss by avoiding filtration and rotary evaporation, simultaneous cell lysis and analyte extraction by ethyl acetate, and the ability to compare whole cultures with their cell pellets and supernatants. Farnesol synthesis and secretion were separable phenomena and pellet:supernatant ratios for farnesol were high, up to 12:1. The assay was validated in terms of precision, specificity, ruggedness, accuracy, solution stability, detection limits (DL), quantitation limits (QL), and dynamic range. The DL for farnesol was 0.02 ng/µl (0.09 µM). Measurement quality was assessed by the relative error of the whole culture versus the sum of pellet and supernatant fractions (WPS). C. albicans strain SC5314 grown at 30 °C in complex and defined media (YPD and mRPMI) was assayed in biological triplicate 17 times over 3 days. Farnesol and the three aromatic fusel alcohols can be measured in the same assay. The levels of all four are greatly altered by the growth medium chosen. Significantly, the three fusel alcohols are synthesized during stationary phase, not during growth. They are secreted quickly without being retained in the cell pellet and may accumulate up to mM concentrations. KEY POINTS: • Quantitative analysis of both intra- and extracellular farnesol, and aromatic fusel oils. • High throughput, whole culture assay with simultaneous lysis and extraction. • Farnesol secretion and synthesis are distinct and separate events. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-12165-w.
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spelling pubmed-95296892022-10-05 Quantitative assay for farnesol and the aromatic fusel alcohols from the fungus Candida albicans Boone, Cory H. T. Gutzmann, Daniel J. Kramer, Jaxon J. Atkin, Audrey L. Nickerson, Kenneth W. Appl Microbiol Biotechnol Methods and Protocols ABSTRACT: The dimorphic fungus Candida albicans is a commensal and opportunistic fungal pathogen of humans. It secretes at least four small lipophilic molecules, farnesol and three aromatic fusel alcohols. Farnesol has been identified as both a quorum sensing molecule (QSM) and a virulence factor. Our gas chromatography (GC)-based assay for these molecules exhibits high throughput, prevention of analyte loss by avoiding filtration and rotary evaporation, simultaneous cell lysis and analyte extraction by ethyl acetate, and the ability to compare whole cultures with their cell pellets and supernatants. Farnesol synthesis and secretion were separable phenomena and pellet:supernatant ratios for farnesol were high, up to 12:1. The assay was validated in terms of precision, specificity, ruggedness, accuracy, solution stability, detection limits (DL), quantitation limits (QL), and dynamic range. The DL for farnesol was 0.02 ng/µl (0.09 µM). Measurement quality was assessed by the relative error of the whole culture versus the sum of pellet and supernatant fractions (WPS). C. albicans strain SC5314 grown at 30 °C in complex and defined media (YPD and mRPMI) was assayed in biological triplicate 17 times over 3 days. Farnesol and the three aromatic fusel alcohols can be measured in the same assay. The levels of all four are greatly altered by the growth medium chosen. Significantly, the three fusel alcohols are synthesized during stationary phase, not during growth. They are secreted quickly without being retained in the cell pellet and may accumulate up to mM concentrations. KEY POINTS: • Quantitative analysis of both intra- and extracellular farnesol, and aromatic fusel oils. • High throughput, whole culture assay with simultaneous lysis and extraction. • Farnesol secretion and synthesis are distinct and separate events. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-12165-w. Springer Berlin Heidelberg 2022-09-15 2022 /pmc/articles/PMC9529689/ /pubmed/36107213 http://dx.doi.org/10.1007/s00253-022-12165-w Text en © The Author(s) 2022 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/) .
spellingShingle Methods and Protocols
Boone, Cory H. T.
Gutzmann, Daniel J.
Kramer, Jaxon J.
Atkin, Audrey L.
Nickerson, Kenneth W.
Quantitative assay for farnesol and the aromatic fusel alcohols from the fungus Candida albicans
title Quantitative assay for farnesol and the aromatic fusel alcohols from the fungus Candida albicans
title_full Quantitative assay for farnesol and the aromatic fusel alcohols from the fungus Candida albicans
title_fullStr Quantitative assay for farnesol and the aromatic fusel alcohols from the fungus Candida albicans
title_full_unstemmed Quantitative assay for farnesol and the aromatic fusel alcohols from the fungus Candida albicans
title_short Quantitative assay for farnesol and the aromatic fusel alcohols from the fungus Candida albicans
title_sort quantitative assay for farnesol and the aromatic fusel alcohols from the fungus candida albicans
topic Methods and Protocols
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529689/
https://www.ncbi.nlm.nih.gov/pubmed/36107213
http://dx.doi.org/10.1007/s00253-022-12165-w
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