Fitzgerald, Shane ORCID: 0000-0002-6570-4485, Furlong, Ciara ORCID: 0000-0002-2949-8688, Holland, Linda ORCID: 0000-0002-0103-0151 and Morrin, Aoife ORCID: 0000-0002-3031-4794 (2022) Multi-strain and -species investigation of volatile metabolites emitted from planktonic and biofilm Candida cultures. Metabolites, 12 (5). ISSN 2218-1989
Abstract
Candida parapsiliosis is a prevalent neonatal pathogen that attains its virulence through its strain-specific ability to form biofilms. The use of volatilomics, the profiling of volatile metabolites from microbes is a non-invasive, simple way to identify and classify microbes; it has shown great potential for pathogen identification. Although C. parapsiliosis is one of the most common clinical fungal pathogens, its volatilome has never been characterised. In this study, planktonic volatilomes of ten clinical strains of C. parapsilosis were analysed, along with a single strain of Candida albicans. Headspace-solid-phase microextraction coupled with gas chromatography-mass spectrometry were employed to analyse the samples. Species-, strain-, and media- influences on the fungal volatilomes were investigated. Twenty-four unique metabolites from the examined Candida spp. (22 from C. albicans; 18 from C. parapsilosis) were included in this study. Chemical classes detected across the samples included alcohols, fatty acid esters, acetates, thiols, sesquiterpenes, and nitrogen-containing compounds. C. albicans volatilomes were most clearly discriminated from C. parapsilosis based on the detection of unique sesquiterpene compounds. The effect of biofilm formation on the C. parapsilosis volatilomes was investigated for the first time by comparing volatilomes of a biofilm-positive strain and a biofilm-negative strain over time (0–48 h) using a novel sampling approach. Volatilomic shifts in the profiles of alcohols, ketones, acids, and acetates were observed specifically in the biofilm-forming samples and attributed to biofilm maturation. This study highlights species-specificity of Candida volatilomes, and also marks the clinical potential for volatilomics for non-invasively detecting fungal pathogens. Additionally, the range of biofilm-specificity across microbial volatilomes is potentially far-reaching, and therefore characterising these volatilomic changes in pathogenic fungal and bacterial biofilms could lead to novel opportunities for detecting severe infections early.
Metadata
Item Type: | Article (Published) |
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Refereed: | Yes |
Uncontrolled Keywords: | volatilomics; Candida; biofilm; fungi; pathogen; gas chromatography; volatile metabolites; solid phase microextraction; mass spectrometry |
Subjects: | Biological Sciences > Microbiology Humanities > Biological Sciences > Microbiology |
DCU Faculties and Centres: | DCU Faculties and Schools > Faculty of Science and Health > School of Biotechnology DCU Faculties and Schools > Faculty of Science and Health > School of Chemical Sciences Research Institutes and Centres > National Centre for Sensor Research (NCSR) Research Institutes and Centres > INSIGHT Centre for Data Analytics |
Publisher: | MDPI |
Official URL: | https://dx.doi.org/10.3390/metabo12050432 |
Copyright Information: | © 2022 The Authors. |
ID Code: | 27443 |
Deposited On: | 27 Jul 2022 17:25 by Thomas Murtagh . Last Modified 15 Mar 2023 16:15 |
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