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Antifungal Activity and Potential Action Mechanism of Allicin against Trichosporon asahii

Trichosporon asahii is an emerging opportunistic pathogen that causes potentially fatal disseminated trichosporonosis. The global prevalence of coronavirus disease 2019 (COVID-19) poses an increasing fungal infection burden caused by T. asahii. Allicin is the main biologically active component with...

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Autores principales: Yang, Xin, Bai, Shuang, Wu, Jiamin, Fan, Yunlong, Zou, Yuekun, Xia, Zhikuan, Ao, Junhong, Chen, Tong, Zhang, Mingwang, Yang, Rongya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269704/
https://www.ncbi.nlm.nih.gov/pubmed/37199655
http://dx.doi.org/10.1128/spectrum.00907-23
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author Yang, Xin
Bai, Shuang
Wu, Jiamin
Fan, Yunlong
Zou, Yuekun
Xia, Zhikuan
Ao, Junhong
Chen, Tong
Zhang, Mingwang
Yang, Rongya
author_facet Yang, Xin
Bai, Shuang
Wu, Jiamin
Fan, Yunlong
Zou, Yuekun
Xia, Zhikuan
Ao, Junhong
Chen, Tong
Zhang, Mingwang
Yang, Rongya
author_sort Yang, Xin
collection PubMed
description Trichosporon asahii is an emerging opportunistic pathogen that causes potentially fatal disseminated trichosporonosis. The global prevalence of coronavirus disease 2019 (COVID-19) poses an increasing fungal infection burden caused by T. asahii. Allicin is the main biologically active component with broad-spectrum antimicrobial activity in garlic. In this study, we performed an in-depth analysis of the antifungal characteristics of allicin against T. asahii based on physiological, cytological, and transcriptomic assessments. In vitro, allicin inhibited the growth of T. asahii planktonic cells and biofilm cells significantly. In vivo, allicin improved the mean survival time of mice with systemic trichosporonosis and reduced tissue fungal burden. Electron microscopy observations clearly demonstrated damage to T. asahii cell morphology and ultrastructure caused by allicin. Furthermore, allicin increased intracellular reactive oxygen species (ROS) accumulation, leading to oxidative stress damage in T. asahii cells. Transcriptome analysis showed that allicin treatment disturbed the biosynthesis of cell membrane and cell wall, glucose catabolism, and oxidative stress. The overexpression of multiple antioxidant enzymes and transporters may also place an additional burden on cells, causing them to collapse. Our findings shed new light on the potential of allicin as an alternative treatment strategy for trichosporonosis. IMPORTANCE Systemic infection caused by T. asahii has recently been recognized as an important cause of mortality in hospitalized COVID-19 patients. Invasive trichosporonosis remains a significant challenge for clinicians, due to the limited therapeutic options. The present work suggests that allicin holds great potential as a therapeutic candidate for T. asahii infection. Allicin demonstrated potent in vitro antifungal activity and potential in vivo protective effects. In addition, transcriptome sequencing provided valuable insights into the antifungal effects of allicin.
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spelling pubmed-102697042023-06-16 Antifungal Activity and Potential Action Mechanism of Allicin against Trichosporon asahii Yang, Xin Bai, Shuang Wu, Jiamin Fan, Yunlong Zou, Yuekun Xia, Zhikuan Ao, Junhong Chen, Tong Zhang, Mingwang Yang, Rongya Microbiol Spectr Research Article Trichosporon asahii is an emerging opportunistic pathogen that causes potentially fatal disseminated trichosporonosis. The global prevalence of coronavirus disease 2019 (COVID-19) poses an increasing fungal infection burden caused by T. asahii. Allicin is the main biologically active component with broad-spectrum antimicrobial activity in garlic. In this study, we performed an in-depth analysis of the antifungal characteristics of allicin against T. asahii based on physiological, cytological, and transcriptomic assessments. In vitro, allicin inhibited the growth of T. asahii planktonic cells and biofilm cells significantly. In vivo, allicin improved the mean survival time of mice with systemic trichosporonosis and reduced tissue fungal burden. Electron microscopy observations clearly demonstrated damage to T. asahii cell morphology and ultrastructure caused by allicin. Furthermore, allicin increased intracellular reactive oxygen species (ROS) accumulation, leading to oxidative stress damage in T. asahii cells. Transcriptome analysis showed that allicin treatment disturbed the biosynthesis of cell membrane and cell wall, glucose catabolism, and oxidative stress. The overexpression of multiple antioxidant enzymes and transporters may also place an additional burden on cells, causing them to collapse. Our findings shed new light on the potential of allicin as an alternative treatment strategy for trichosporonosis. IMPORTANCE Systemic infection caused by T. asahii has recently been recognized as an important cause of mortality in hospitalized COVID-19 patients. Invasive trichosporonosis remains a significant challenge for clinicians, due to the limited therapeutic options. The present work suggests that allicin holds great potential as a therapeutic candidate for T. asahii infection. Allicin demonstrated potent in vitro antifungal activity and potential in vivo protective effects. In addition, transcriptome sequencing provided valuable insights into the antifungal effects of allicin. American Society for Microbiology 2023-05-18 /pmc/articles/PMC10269704/ /pubmed/37199655 http://dx.doi.org/10.1128/spectrum.00907-23 Text en Copyright © 2023 Yang et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Yang, Xin
Bai, Shuang
Wu, Jiamin
Fan, Yunlong
Zou, Yuekun
Xia, Zhikuan
Ao, Junhong
Chen, Tong
Zhang, Mingwang
Yang, Rongya
Antifungal Activity and Potential Action Mechanism of Allicin against Trichosporon asahii
title Antifungal Activity and Potential Action Mechanism of Allicin against Trichosporon asahii
title_full Antifungal Activity and Potential Action Mechanism of Allicin against Trichosporon asahii
title_fullStr Antifungal Activity and Potential Action Mechanism of Allicin against Trichosporon asahii
title_full_unstemmed Antifungal Activity and Potential Action Mechanism of Allicin against Trichosporon asahii
title_short Antifungal Activity and Potential Action Mechanism of Allicin against Trichosporon asahii
title_sort antifungal activity and potential action mechanism of allicin against trichosporon asahii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269704/
https://www.ncbi.nlm.nih.gov/pubmed/37199655
http://dx.doi.org/10.1128/spectrum.00907-23
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