The <i>SsAtg1</i> Activating Autophagy Is Required for Sclerotia Formation and Pathogenicity in <i>Sclerotinia sclerotiorum</i>

<i>Sclerotinia sclerotiorum</i> is a necrotrophic phytopathogenic fungus that produces sclerotia. Sclerotia are essential components of the survival and disease cycle of this devastating pathogen. In this study, we analyzed comparative transcriptomics of hyphae and sclerotia. A total of...

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Main Authors: Wenli Jiao, Huilin Yu, Xueting Chen, Kunqin Xiao, Dongmei Jia, Fengting Wang, Yanhua Zhang, Hongyu Pan
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Journal of Fungi
Subjects:
Online Access:https://www.mdpi.com/2309-608X/8/12/1314
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author Wenli Jiao
Huilin Yu
Xueting Chen
Kunqin Xiao
Dongmei Jia
Fengting Wang
Yanhua Zhang
Hongyu Pan
author_facet Wenli Jiao
Huilin Yu
Xueting Chen
Kunqin Xiao
Dongmei Jia
Fengting Wang
Yanhua Zhang
Hongyu Pan
author_sort Wenli Jiao
collection DOAJ
description <i>Sclerotinia sclerotiorum</i> is a necrotrophic phytopathogenic fungus that produces sclerotia. Sclerotia are essential components of the survival and disease cycle of this devastating pathogen. In this study, we analyzed comparative transcriptomics of hyphae and sclerotia. A total of 1959 differentially expressed genes, 919 down-regulated and 1040 up-regulated, were identified. Transcriptomes data provide the possibility to precisely comprehend the sclerotia development. We further analyzed the differentially expressed genes (DEGs) in sclerotia to explore the molecular mechanism of sclerotia development, which include ribosome biogenesis and translation, melanin biosynthesis, autophagy and reactivate oxygen metabolism. Among these, the autophagy-related gene <i>SsAtg1</i> was up-regulated in sclerotia. Atg1 homologs play critical roles in autophagy, a ubiquitous and evolutionarily highly conserved cellular mechanism for turnover of intracellular materials in eukaryotes. Therefore, we investigated the function of <i>SsAtg1</i> to explore the function of the autophagy pathway in <i>S. sclerotiorum</i>. Deficiency of <i>SsAtg1</i> inhibited autophagosome accumulation in the vacuoles of nitrogen-starved cells. Notably, Δ<i>SsAtg1</i> was unable to form sclerotia and displayed defects in vegetative growth under conditions of nutrient restriction. Furthermore, the development and penetration of the compound appressoria in Δ<i>SsAtg1</i> was abnormal. Pathogenicity analysis showed that <i>SsAtg1</i> was required for full virulence of <i>S. sclerotiorum</i>. Taken together, these results indicate that <i>SsAtg1</i> is a core autophagy-related gene that has vital functions in nutrient utilization, sclerotia development and pathogenicity in <i>S. sclerotiorum</i>.
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spelling doaj.art-04aff41495624764aae0f61dd19b25602023-11-24T16:00:21ZengMDPI AGJournal of Fungi2309-608X2022-12-01812131410.3390/jof8121314The <i>SsAtg1</i> Activating Autophagy Is Required for Sclerotia Formation and Pathogenicity in <i>Sclerotinia sclerotiorum</i>Wenli Jiao0Huilin Yu1Xueting Chen2Kunqin Xiao3Dongmei Jia4Fengting Wang5Yanhua Zhang6Hongyu Pan7College of Plant Sciences, Jilin University, Changchun 130012, ChinaCollege of Plant Sciences, Jilin University, Changchun 130012, ChinaCollege of Plant Sciences, Jilin University, Changchun 130012, ChinaCollege of Plant Sciences, Jilin University, Changchun 130012, ChinaCollege of Plant Sciences, Jilin University, Changchun 130012, ChinaCollege of Plant Sciences, Jilin University, Changchun 130012, ChinaCollege of Plant Sciences, Jilin University, Changchun 130012, ChinaCollege of Plant Sciences, Jilin University, Changchun 130012, China<i>Sclerotinia sclerotiorum</i> is a necrotrophic phytopathogenic fungus that produces sclerotia. Sclerotia are essential components of the survival and disease cycle of this devastating pathogen. In this study, we analyzed comparative transcriptomics of hyphae and sclerotia. A total of 1959 differentially expressed genes, 919 down-regulated and 1040 up-regulated, were identified. Transcriptomes data provide the possibility to precisely comprehend the sclerotia development. We further analyzed the differentially expressed genes (DEGs) in sclerotia to explore the molecular mechanism of sclerotia development, which include ribosome biogenesis and translation, melanin biosynthesis, autophagy and reactivate oxygen metabolism. Among these, the autophagy-related gene <i>SsAtg1</i> was up-regulated in sclerotia. Atg1 homologs play critical roles in autophagy, a ubiquitous and evolutionarily highly conserved cellular mechanism for turnover of intracellular materials in eukaryotes. Therefore, we investigated the function of <i>SsAtg1</i> to explore the function of the autophagy pathway in <i>S. sclerotiorum</i>. Deficiency of <i>SsAtg1</i> inhibited autophagosome accumulation in the vacuoles of nitrogen-starved cells. Notably, Δ<i>SsAtg1</i> was unable to form sclerotia and displayed defects in vegetative growth under conditions of nutrient restriction. Furthermore, the development and penetration of the compound appressoria in Δ<i>SsAtg1</i> was abnormal. Pathogenicity analysis showed that <i>SsAtg1</i> was required for full virulence of <i>S. sclerotiorum</i>. Taken together, these results indicate that <i>SsAtg1</i> is a core autophagy-related gene that has vital functions in nutrient utilization, sclerotia development and pathogenicity in <i>S. sclerotiorum</i>.https://www.mdpi.com/2309-608X/8/12/1314<i>Sclerotinia sclerotiorum</i>transcriptome<i>SsAtg1</i>sclerotiaautophagypathogenicity
spellingShingle Wenli Jiao
Huilin Yu
Xueting Chen
Kunqin Xiao
Dongmei Jia
Fengting Wang
Yanhua Zhang
Hongyu Pan
The <i>SsAtg1</i> Activating Autophagy Is Required for Sclerotia Formation and Pathogenicity in <i>Sclerotinia sclerotiorum</i>
Journal of Fungi
<i>Sclerotinia sclerotiorum</i>
transcriptome
<i>SsAtg1</i>
sclerotia
autophagy
pathogenicity
title The <i>SsAtg1</i> Activating Autophagy Is Required for Sclerotia Formation and Pathogenicity in <i>Sclerotinia sclerotiorum</i>
title_full The <i>SsAtg1</i> Activating Autophagy Is Required for Sclerotia Formation and Pathogenicity in <i>Sclerotinia sclerotiorum</i>
title_fullStr The <i>SsAtg1</i> Activating Autophagy Is Required for Sclerotia Formation and Pathogenicity in <i>Sclerotinia sclerotiorum</i>
title_full_unstemmed The <i>SsAtg1</i> Activating Autophagy Is Required for Sclerotia Formation and Pathogenicity in <i>Sclerotinia sclerotiorum</i>
title_short The <i>SsAtg1</i> Activating Autophagy Is Required for Sclerotia Formation and Pathogenicity in <i>Sclerotinia sclerotiorum</i>
title_sort i ssatg1 i activating autophagy is required for sclerotia formation and pathogenicity in i sclerotinia sclerotiorum i
topic <i>Sclerotinia sclerotiorum</i>
transcriptome
<i>SsAtg1</i>
sclerotia
autophagy
pathogenicity
url https://www.mdpi.com/2309-608X/8/12/1314
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