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MoPer1 is required for growth, conidiogenesis, and pathogenicity in Magnaporthe oryzae

BACKGROUND: GPI-anchoring is a prevalent Glycosylphosphatidylinositol modification process of posttranslational protein and is necessary for cell wall integrity in eukaryotes. To date, the function of GPI anchored-related protein remains unknown in phytopathogenic fungi. RESULTS: We here characteriz...

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Autores principales: Chen, Yue, Wu, Xiyang, Li, Chenggang, Zeng, Yibo, Tan, Xinqiu, Zhang, Deyong, Liu, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303226/
https://www.ncbi.nlm.nih.gov/pubmed/30578458
http://dx.doi.org/10.1186/s12284-018-0255-9
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author Chen, Yue
Wu, Xiyang
Li, Chenggang
Zeng, Yibo
Tan, Xinqiu
Zhang, Deyong
Liu, Yong
author_facet Chen, Yue
Wu, Xiyang
Li, Chenggang
Zeng, Yibo
Tan, Xinqiu
Zhang, Deyong
Liu, Yong
author_sort Chen, Yue
collection PubMed
description BACKGROUND: GPI-anchoring is a prevalent Glycosylphosphatidylinositol modification process of posttranslational protein and is necessary for cell wall integrity in eukaryotes. To date, the function of GPI anchored-related protein remains unknown in phytopathogenic fungi. RESULTS: We here characterized the functions of MoPer1, a homolog of Saccharomyces cerevisiae ScPer1, from the rice blast fungus Magnaporthe oryzae. Transcriptional analysis demonstrated that MoPER1 was significantly upregulated during conidiation and infection. We found that the ∆Moper1 mutant was defective in conidiation and appressoria formation, and MoPer1 was involved in osmotic stress response and maintaining the cell wall integrity. Pathogenicity assays indicated that deletion of MoPEP1 significant reduction in virulence. Microscopic examination of the lesions revealed that the invasive hyphae of ∆Moper1 mutants were mostly restricted to the primary infected leaf sheath cells. CONCLUSIONS: Our results indicated that MoPer1 is necessary for growth, conidiogenesis, and pathogenicity of the fungus. Our study facilitated to deep elucidate the pathogenic molecular mechanism of M. oryzae, and also provided a very helpful reference value for developing effective fungicide pointed at as the gene for target. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12284-018-0255-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-63032262019-01-04 MoPer1 is required for growth, conidiogenesis, and pathogenicity in Magnaporthe oryzae Chen, Yue Wu, Xiyang Li, Chenggang Zeng, Yibo Tan, Xinqiu Zhang, Deyong Liu, Yong Rice (N Y) Original Article BACKGROUND: GPI-anchoring is a prevalent Glycosylphosphatidylinositol modification process of posttranslational protein and is necessary for cell wall integrity in eukaryotes. To date, the function of GPI anchored-related protein remains unknown in phytopathogenic fungi. RESULTS: We here characterized the functions of MoPer1, a homolog of Saccharomyces cerevisiae ScPer1, from the rice blast fungus Magnaporthe oryzae. Transcriptional analysis demonstrated that MoPER1 was significantly upregulated during conidiation and infection. We found that the ∆Moper1 mutant was defective in conidiation and appressoria formation, and MoPer1 was involved in osmotic stress response and maintaining the cell wall integrity. Pathogenicity assays indicated that deletion of MoPEP1 significant reduction in virulence. Microscopic examination of the lesions revealed that the invasive hyphae of ∆Moper1 mutants were mostly restricted to the primary infected leaf sheath cells. CONCLUSIONS: Our results indicated that MoPer1 is necessary for growth, conidiogenesis, and pathogenicity of the fungus. Our study facilitated to deep elucidate the pathogenic molecular mechanism of M. oryzae, and also provided a very helpful reference value for developing effective fungicide pointed at as the gene for target. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12284-018-0255-9) contains supplementary material, which is available to authorized users. Springer US 2018-12-22 /pmc/articles/PMC6303226/ /pubmed/30578458 http://dx.doi.org/10.1186/s12284-018-0255-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Chen, Yue
Wu, Xiyang
Li, Chenggang
Zeng, Yibo
Tan, Xinqiu
Zhang, Deyong
Liu, Yong
MoPer1 is required for growth, conidiogenesis, and pathogenicity in Magnaporthe oryzae
title MoPer1 is required for growth, conidiogenesis, and pathogenicity in Magnaporthe oryzae
title_full MoPer1 is required for growth, conidiogenesis, and pathogenicity in Magnaporthe oryzae
title_fullStr MoPer1 is required for growth, conidiogenesis, and pathogenicity in Magnaporthe oryzae
title_full_unstemmed MoPer1 is required for growth, conidiogenesis, and pathogenicity in Magnaporthe oryzae
title_short MoPer1 is required for growth, conidiogenesis, and pathogenicity in Magnaporthe oryzae
title_sort moper1 is required for growth, conidiogenesis, and pathogenicity in magnaporthe oryzae
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303226/
https://www.ncbi.nlm.nih.gov/pubmed/30578458
http://dx.doi.org/10.1186/s12284-018-0255-9
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