Metabolomic analysis of Trichophyton rubrum and Microsporum canis during keratin degradation

Abstract Keratin is important and needed for the growth of dermatophytes in the host tissue. In turn, the ability to invade keratinised tissues is defined as a pivotal virulence attribute of this group of medically important fungi. The host–dermatophyte interaction is accompanied by an adaptation of...

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Autores principales: Anita Ciesielska, Anna Kawa, Katarzyna Kanarek, Adrian Soboń, Rafał Szewczyk
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/6371ab0b28dc4c8cbe05f95dcba4c63c
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spelling oai:doaj.org-article:6371ab0b28dc4c8cbe05f95dcba4c63c2021-12-02T12:11:12ZMetabolomic analysis of Trichophyton rubrum and Microsporum canis during keratin degradation10.1038/s41598-021-83632-z2045-2322https://doaj.org/article/6371ab0b28dc4c8cbe05f95dcba4c63c2021-02-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-83632-zhttps://doaj.org/toc/2045-2322Abstract Keratin is important and needed for the growth of dermatophytes in the host tissue. In turn, the ability to invade keratinised tissues is defined as a pivotal virulence attribute of this group of medically important fungi. The host–dermatophyte interaction is accompanied by an adaptation of fungal metabolism that allows them to adhere to the host tissue as well as utilize the available nutrients necessary for their survival and growth. Dermatophyte infections pose a significant epidemiological and clinical problem. Trichophyton rubrum is the most common anthropophilic dermatophyte worldwide and its typical infection areas include skin of hands or feet and nail plate. In turn, Microsporum canis is a zoophilic pathogen, and mostly well known for ringworm in pets, it is also known to infect humans. The aim of the study was to compare the intracellular metabolite content in the T. rubrum and M. canis during keratin degradation using liquid chromatography system coupled with tandem mass spectrometer (LC-MS/MS). The metabolite “fingerprints” revealed compounds associated with amino acids metabolism, carbohydrate metabolism related to the glycolysis and the tricarboxylic acid cycle (TCA), as well as nucleotide and energy metabolism. The metabolites such as kynurenic acid, l-alanine and cysteine in case of T. rubrum as well as cysteine and riboflavin in case of M. canis were detected only during keratin degradation what may suggest that these compounds may play a key role in the interactions of T. rubrum and M. canis with the host tissue. The metabolomic results were completed by qPCR gene expression assay. Our findings suggest that metabolomic analysis of T. rubrum and M. canis growing in culture media that mimic the dermatophyte infection could allow the understanding of processes involved in the pathogenesis of dermatophytes.Anita CiesielskaAnna KawaKatarzyna KanarekAdrian SobońRafał SzewczykNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Anita Ciesielska
Anna Kawa
Katarzyna Kanarek
Adrian Soboń
Rafał Szewczyk
Metabolomic analysis of Trichophyton rubrum and Microsporum canis during keratin degradation
description Abstract Keratin is important and needed for the growth of dermatophytes in the host tissue. In turn, the ability to invade keratinised tissues is defined as a pivotal virulence attribute of this group of medically important fungi. The host–dermatophyte interaction is accompanied by an adaptation of fungal metabolism that allows them to adhere to the host tissue as well as utilize the available nutrients necessary for their survival and growth. Dermatophyte infections pose a significant epidemiological and clinical problem. Trichophyton rubrum is the most common anthropophilic dermatophyte worldwide and its typical infection areas include skin of hands or feet and nail plate. In turn, Microsporum canis is a zoophilic pathogen, and mostly well known for ringworm in pets, it is also known to infect humans. The aim of the study was to compare the intracellular metabolite content in the T. rubrum and M. canis during keratin degradation using liquid chromatography system coupled with tandem mass spectrometer (LC-MS/MS). The metabolite “fingerprints” revealed compounds associated with amino acids metabolism, carbohydrate metabolism related to the glycolysis and the tricarboxylic acid cycle (TCA), as well as nucleotide and energy metabolism. The metabolites such as kynurenic acid, l-alanine and cysteine in case of T. rubrum as well as cysteine and riboflavin in case of M. canis were detected only during keratin degradation what may suggest that these compounds may play a key role in the interactions of T. rubrum and M. canis with the host tissue. The metabolomic results were completed by qPCR gene expression assay. Our findings suggest that metabolomic analysis of T. rubrum and M. canis growing in culture media that mimic the dermatophyte infection could allow the understanding of processes involved in the pathogenesis of dermatophytes.
format article
author Anita Ciesielska
Anna Kawa
Katarzyna Kanarek
Adrian Soboń
Rafał Szewczyk
author_facet Anita Ciesielska
Anna Kawa
Katarzyna Kanarek
Adrian Soboń
Rafał Szewczyk
author_sort Anita Ciesielska
title Metabolomic analysis of Trichophyton rubrum and Microsporum canis during keratin degradation
title_short Metabolomic analysis of Trichophyton rubrum and Microsporum canis during keratin degradation
title_full Metabolomic analysis of Trichophyton rubrum and Microsporum canis during keratin degradation
title_fullStr Metabolomic analysis of Trichophyton rubrum and Microsporum canis during keratin degradation
title_full_unstemmed Metabolomic analysis of Trichophyton rubrum and Microsporum canis during keratin degradation
title_sort metabolomic analysis of trichophyton rubrum and microsporum canis during keratin degradation
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/6371ab0b28dc4c8cbe05f95dcba4c63c
work_keys_str_mv AT anitaciesielska metabolomicanalysisoftrichophytonrubrumandmicrosporumcanisduringkeratindegradation
AT annakawa metabolomicanalysisoftrichophytonrubrumandmicrosporumcanisduringkeratindegradation
AT katarzynakanarek metabolomicanalysisoftrichophytonrubrumandmicrosporumcanisduringkeratindegradation
AT adriansobon metabolomicanalysisoftrichophytonrubrumandmicrosporumcanisduringkeratindegradation
AT rafałszewczyk metabolomicanalysisoftrichophytonrubrumandmicrosporumcanisduringkeratindegradation
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