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Published on: October 23, 2016
Endosomal sorting complexes required for transport-0 (ESCRT-0) are essential for fungal development, pathogenicity,
Li-Xiao Sun1, Hui Qian1, Meng-Yu Liu1
1State Key Laboratory for Managing Biotic and Chemical Treats to the Quality and Safety of Agro-products, Institute of Biotechnology, Zhejiang University, Hangzhou, 310058, China.
Abstract:
Magnaporthe oryzae is an important plant pathogen that causes rice blast. Hse1 and Vps27 are components of ESCRT-0 involved in the multivesicular body (MVB) sorting pathway and biogenesis. To date, the biological functions of ESCRT-0 in M. oryzae have not been determined. In this study, we identified and characterized Hse1 and Vps27 in M. oryzae. Disruption of MoHse1 and MoVps27 caused pleiotropic defects in growth, conidiation, sexual development and pathogenicity, thereby resulting in loss of virulence in rice and barley leaves. Disruption of MoHse1 and MoVps27 triggered increased lipidation of MoAtg8 and degradation of GFP-MoAtg8, indicating that ESCRT-0 is involved in the regulation of autophagy. ESCRT-0 was determined to interact with coat protein complex II (COPII), a regulator functioning in homeostasis of the endoplasmic reticulum (ER homeostasis), and disruption of MoHse1 and MoVps27 also blocked activation of the unfolded protein response (UPR) and autophagy of the endoplasmic reticulum (ER-phagy). Overall, our results indicate that ESCRT-0 plays critical roles in regulating fungal development, virulence, autophagy and ER-phagy in M. oryzae.
Insights
The ESCRT-0 complex, comprising Hse1 and Vps27, is crucial for regulating the growth, virulence, and essential cellular processes like autophagy and ER-phagy in the rice blast fungus Magnaporthe oryzae.
Area of Science:
- Molecular Mycology
- Cell Biology
- Plant Pathology
Background:
- Magnaporthe oryzae causes devastating rice blast disease.
- ESCRT-0 complex (Hse1, Vps27) is vital for multivesicular body (MVB) biogenesis.
- ESCRT-0 functions in M. oryzae remain largely uncharacterized.
Purpose of the Study:
- To identify and functionally characterize Hse1 and Vps27 in M. oryzae.
- To elucidate the role of ESCRT-0 in fungal development and pathogenicity.
- To investigate ESCRT-0 involvement in autophagy and ER homeostasis.
Main Methods:
- Gene disruption of MoHse1 and MoVps27.
- Phenotypic analysis of mutant strains (growth, conidiation, development, pathogenicity).
- Analysis of autophagy markers (MoAtg8 lipidation, GFP-MoAtg8 degradation) and ER stress responses (UPR, ER-phagy).
Main Results:
- Disruption of MoHse1 and MoVps27 led to severe defects in growth, development, and pathogenicity, causing loss of virulence.
- ESCRT-0 mutants exhibited dysregulated autophagy, evidenced by altered MoAtg8 lipidation and degradation.
- ESCRT-0 interacts with COPII, and its disruption impaired UPR and ER-phagy.
Conclusions:
- ESCRT-0 is essential for M. oryzae development, virulence, and maintaining cellular homeostasis.
- ESCRT-0 regulates autophagy and ER-phagy pathways in M. oryzae.
- Targeting ESCRT-0 could be a strategy to control rice blast disease.
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