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  4. The antimicrobial photodynamic inactivation resistance of Candida albicans is modulated by the Hog1 pathway and the Cap1 transcription factor
 
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The antimicrobial photodynamic inactivation resistance of Candida albicans is modulated by the Hog1 pathway and the Cap1 transcription factor

Journal
Medical mycology
Journal Volume
57
Journal Issue
5
Pages
618-627
Date Issued
2019
Author(s)
Chien, C.-T.
Chen, Y.-C.
Liu, Y.-C.
Liang, S.-H.
Lin, H.-H.
CHING-HSUAN LIN  
DOI
10.1093/mmy/myy079
URI
https://www.scopus.com/inward/record.url?eid=2-s2.0-85072387466&partnerID=40&md5=133a4b0b521a5e9e354b9f229255763c
https://scholars.lib.ntu.edu.tw/handle/123456789/535651
Abstract
Candida albicans is the most important fungal pathogen afflicting humans, particularly immunocompromised patients. However, currently available antifungal drugs are limited and ineffective against drug-resistant strains. The development of new drugs or alternative therapeutic approaches to control fungal infections is urgent and necessary. Photodynamic inactivation (PDI) is a new promising therapy for eradicating microorganism infections through combining visible light, photosensitizers, and oxygen to generate reactive oxygen species (ROS). Although cytoprotective responses induced by photodynamic therapy (PDT) have been well studied in cancer cells, the mechanisms by which C. albicans responds to PDI are largely unknown. In this study, we first demonstrated that PDI induces C. albicans Hog1p activation. Deletion of any of the SSK2, PBS2, and HOG1 genes significantly decreased the survival rate after photochemical reactions, indicating that the Hog1 SAPK pathway is required for tolerance to PDI. Furthermore, the basic leucine zipper transcription factor Cap1 that regulates several downstream antioxidant genes was highly expressed during the response to PDI, and loss of CAP1 also resulted in decreased C. albicans survival rates. This study demonstrates the importance of the Hog1 SAPK and the Cap1 transcription factor, which regulates in resistance to PDI-mediated oxidative stress in C. albicans. Understanding the mechanisms by which C. albicans responds to PDI and consequently scavenges ROS will be very useful for the further development of therapeutics to control fungal infectious diseases, particularly those of the skin and mucosal infections. ? The Author(s) 2018.
Subjects
Antimicrobial photodynamic inactivation; Candida albicans; Cap1; Hog1
SDGs

[SDGs]SDG3

Other Subjects
basic leucine zipper transcription factor; reactive oxygen metabolite; stress activated protein kinase; tolonium chloride; transcription factor; transcription factor Cap1; unclassified drug; Article; Candida albicans; controlled study; gene; gene deletion; gene expression; Hog1 gene; nonhuman; oxidative stress; PBS2 gene; photodynamic therapy; SSK2 gene; survival rate
Type
journal article

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