The Lack of SNARE Protein Homolog Syn8 Influences Biofilm Formation of Candida glabrata

Biofilm formation of Candida species is considered to be a pathogenic factor of host infection. Since biofilm formation of Candida glabrata has not been as well studied as that of Candida albicans, we performed genetic screening of C. glabrata, and three candidate genes associated with biofilm forma...

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Main Authors: Xinyue Chen, Shun Iwatani, Toshitaka Kitamoto, Hiroji Chibana, Susumu Kajiwara
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-02-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2021.607188/full
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spelling doaj-3c650174122b4a44834c6c7b179382152021-02-12T05:15:20ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-02-01910.3389/fcell.2021.607188607188The Lack of SNARE Protein Homolog Syn8 Influences Biofilm Formation of Candida glabrataXinyue Chen0Shun Iwatani1Toshitaka Kitamoto2Hiroji Chibana3Susumu Kajiwara4School of Life Sciences and Technology, Tokyo Institute of Technology, Yokohama, JapanSchool of Life Sciences and Technology, Tokyo Institute of Technology, Yokohama, JapanSchool of Materials and Chemical Technology, Tokyo Institute of Technology, Yokohama, JapanMedical Mycology Research Center, Chiba University, Chiba, JapanSchool of Life Sciences and Technology, Tokyo Institute of Technology, Yokohama, JapanBiofilm formation of Candida species is considered to be a pathogenic factor of host infection. Since biofilm formation of Candida glabrata has not been as well studied as that of Candida albicans, we performed genetic screening of C. glabrata, and three candidate genes associated with biofilm formation were identified. Candida glabrata SYN8 (CAGL0H06325g) was selected as the most induced gene in biofilm cells for further research. Our results indicated that the syn8Δ mutant was defective not only in biofilm metabolic activity but also in biofilm morphological structure and biomass. Deletion of SYN8 seemed to have no effect on extracellular matrix production, but it led to a notable decrease in adhesion ability during biofilm formation, which may be linked to the repression of two adhesin genes, EPA10 and EPA22. Furthermore, hypersensitivity to hygromycin B and various ions in addition to the abnormal vacuolar morphology in the syn8Δ mutant suggested that active vacuolar function is required for biofilm formation of C. glabrata. These findings enhance our understanding of biofilm formation in this fungus and provide information for the development of future clinical treatments.https://www.frontiersin.org/articles/10.3389/fcell.2021.607188/fullCandida glabratabiofilm formationgenetic screeningSNARE proteinvacuole
collection DOAJ
language English
format Article
sources DOAJ
author Xinyue Chen
Shun Iwatani
Toshitaka Kitamoto
Hiroji Chibana
Susumu Kajiwara
spellingShingle Xinyue Chen
Shun Iwatani
Toshitaka Kitamoto
Hiroji Chibana
Susumu Kajiwara
The Lack of SNARE Protein Homolog Syn8 Influences Biofilm Formation of Candida glabrata
Frontiers in Cell and Developmental Biology
Candida glabrata
biofilm formation
genetic screening
SNARE protein
vacuole
author_facet Xinyue Chen
Shun Iwatani
Toshitaka Kitamoto
Hiroji Chibana
Susumu Kajiwara
author_sort Xinyue Chen
title The Lack of SNARE Protein Homolog Syn8 Influences Biofilm Formation of Candida glabrata
title_short The Lack of SNARE Protein Homolog Syn8 Influences Biofilm Formation of Candida glabrata
title_full The Lack of SNARE Protein Homolog Syn8 Influences Biofilm Formation of Candida glabrata
title_fullStr The Lack of SNARE Protein Homolog Syn8 Influences Biofilm Formation of Candida glabrata
title_full_unstemmed The Lack of SNARE Protein Homolog Syn8 Influences Biofilm Formation of Candida glabrata
title_sort lack of snare protein homolog syn8 influences biofilm formation of candida glabrata
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2021-02-01
description Biofilm formation of Candida species is considered to be a pathogenic factor of host infection. Since biofilm formation of Candida glabrata has not been as well studied as that of Candida albicans, we performed genetic screening of C. glabrata, and three candidate genes associated with biofilm formation were identified. Candida glabrata SYN8 (CAGL0H06325g) was selected as the most induced gene in biofilm cells for further research. Our results indicated that the syn8Δ mutant was defective not only in biofilm metabolic activity but also in biofilm morphological structure and biomass. Deletion of SYN8 seemed to have no effect on extracellular matrix production, but it led to a notable decrease in adhesion ability during biofilm formation, which may be linked to the repression of two adhesin genes, EPA10 and EPA22. Furthermore, hypersensitivity to hygromycin B and various ions in addition to the abnormal vacuolar morphology in the syn8Δ mutant suggested that active vacuolar function is required for biofilm formation of C. glabrata. These findings enhance our understanding of biofilm formation in this fungus and provide information for the development of future clinical treatments.
topic Candida glabrata
biofilm formation
genetic screening
SNARE protein
vacuole
url https://www.frontiersin.org/articles/10.3389/fcell.2021.607188/full
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