Cargando…

Magnaporthe oryzae Chloroplast Targeting Endo-β-1,4-Xylanase I MoXYL1A Regulates Conidiation, Appressorium Maturation and Virulence of the Rice Blast Fungus

Endo-β-1,4-Xylanases are a group of extracellular enzymes that catalyze the hydrolysis of xylan, a principal constituent of the plant primary cell wall. The contribution of Endo-β-1,4-Xylanase I to both physiology and pathogenesis of the rice blast fungus M. oryzae is unknown. Here, we characterized...

Descripción completa

Detalles Bibliográficos
Autores principales: Shabbir, Ammarah, Batool, Wajjiha, Yu, Dan, Lin, Lili, An, Qiuli, Xiaomin, Chen, Guo, Hengyuan, Yuan, Shuangshuang, Malota, Sekete, Wang, Zonghua, Norvienyeku, Justice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374862/
https://www.ncbi.nlm.nih.gov/pubmed/35960402
http://dx.doi.org/10.1186/s12284-022-00584-2
_version_ 1784767869230252032
author Shabbir, Ammarah
Batool, Wajjiha
Yu, Dan
Lin, Lili
An, Qiuli
Xiaomin, Chen
Guo, Hengyuan
Yuan, Shuangshuang
Malota, Sekete
Wang, Zonghua
Norvienyeku, Justice
author_facet Shabbir, Ammarah
Batool, Wajjiha
Yu, Dan
Lin, Lili
An, Qiuli
Xiaomin, Chen
Guo, Hengyuan
Yuan, Shuangshuang
Malota, Sekete
Wang, Zonghua
Norvienyeku, Justice
author_sort Shabbir, Ammarah
collection PubMed
description Endo-β-1,4-Xylanases are a group of extracellular enzymes that catalyze the hydrolysis of xylan, a principal constituent of the plant primary cell wall. The contribution of Endo-β-1,4-Xylanase I to both physiology and pathogenesis of the rice blast fungus M. oryzae is unknown. Here, we characterized the biological function of two endoxylanase I (MoXYL1A and MoXYL1B) genes in the development of M. oryzae using targeted gene deletion, biochemical analysis, and fluorescence microscopy. Phenotypic analysis of ∆Moxyl1A strains showed that MoXYL1A is required for the full virulence of M. oryzae but is dispensable for the vegetative growth of the rice blast fungus. MoXYL1B, in contrast, did not have a clear role in the infectious cycle but has a critical function in asexual reproduction of the fungus. The double deletion mutant was severely impaired in pathogenicity and virulence as well as asexual development. We found that MoXYL1A deletion compromised appressorium morphogenesis and function, leading to failure to penetrate host cells. Fluorescently tagged MoXYL1A and MoXYL1B displayed cytoplasmic localization in M. oryzae, while analysis of MoXYL1A-GFP and MoXYL1B-GFP in-planta revealed translocation and accumulation of these effector proteins into host cells. Meanwhile, sequence feature analysis showed that MoXYL1A possesses a transient chloroplast targeting signal peptide, and results from an Agrobacterium infiltration assay confirmed co-localization of MoXYL1A-GFP with ChCPN10C-RFP in the chloroplasts of host cells. MoXYL1B, accumulated to the cytoplasm of the host. Taken together, we conclude that MoXYL1A is a secreted effector protein that likely promotes the virulence of M. oryzae by interfering in the proper functioning of the host chloroplast, while the related xylanase MoXYL1B does not have a major role in virulence of M. oryzae. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12284-022-00584-2.
format Online
Article
Text
id pubmed-9374862
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-93748622022-08-14 Magnaporthe oryzae Chloroplast Targeting Endo-β-1,4-Xylanase I MoXYL1A Regulates Conidiation, Appressorium Maturation and Virulence of the Rice Blast Fungus Shabbir, Ammarah Batool, Wajjiha Yu, Dan Lin, Lili An, Qiuli Xiaomin, Chen Guo, Hengyuan Yuan, Shuangshuang Malota, Sekete Wang, Zonghua Norvienyeku, Justice Rice (N Y) Original Article Endo-β-1,4-Xylanases are a group of extracellular enzymes that catalyze the hydrolysis of xylan, a principal constituent of the plant primary cell wall. The contribution of Endo-β-1,4-Xylanase I to both physiology and pathogenesis of the rice blast fungus M. oryzae is unknown. Here, we characterized the biological function of two endoxylanase I (MoXYL1A and MoXYL1B) genes in the development of M. oryzae using targeted gene deletion, biochemical analysis, and fluorescence microscopy. Phenotypic analysis of ∆Moxyl1A strains showed that MoXYL1A is required for the full virulence of M. oryzae but is dispensable for the vegetative growth of the rice blast fungus. MoXYL1B, in contrast, did not have a clear role in the infectious cycle but has a critical function in asexual reproduction of the fungus. The double deletion mutant was severely impaired in pathogenicity and virulence as well as asexual development. We found that MoXYL1A deletion compromised appressorium morphogenesis and function, leading to failure to penetrate host cells. Fluorescently tagged MoXYL1A and MoXYL1B displayed cytoplasmic localization in M. oryzae, while analysis of MoXYL1A-GFP and MoXYL1B-GFP in-planta revealed translocation and accumulation of these effector proteins into host cells. Meanwhile, sequence feature analysis showed that MoXYL1A possesses a transient chloroplast targeting signal peptide, and results from an Agrobacterium infiltration assay confirmed co-localization of MoXYL1A-GFP with ChCPN10C-RFP in the chloroplasts of host cells. MoXYL1B, accumulated to the cytoplasm of the host. Taken together, we conclude that MoXYL1A is a secreted effector protein that likely promotes the virulence of M. oryzae by interfering in the proper functioning of the host chloroplast, while the related xylanase MoXYL1B does not have a major role in virulence of M. oryzae. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12284-022-00584-2. Springer US 2022-08-12 /pmc/articles/PMC9374862/ /pubmed/35960402 http://dx.doi.org/10.1186/s12284-022-00584-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Shabbir, Ammarah
Batool, Wajjiha
Yu, Dan
Lin, Lili
An, Qiuli
Xiaomin, Chen
Guo, Hengyuan
Yuan, Shuangshuang
Malota, Sekete
Wang, Zonghua
Norvienyeku, Justice
Magnaporthe oryzae Chloroplast Targeting Endo-β-1,4-Xylanase I MoXYL1A Regulates Conidiation, Appressorium Maturation and Virulence of the Rice Blast Fungus
title Magnaporthe oryzae Chloroplast Targeting Endo-β-1,4-Xylanase I MoXYL1A Regulates Conidiation, Appressorium Maturation and Virulence of the Rice Blast Fungus
title_full Magnaporthe oryzae Chloroplast Targeting Endo-β-1,4-Xylanase I MoXYL1A Regulates Conidiation, Appressorium Maturation and Virulence of the Rice Blast Fungus
title_fullStr Magnaporthe oryzae Chloroplast Targeting Endo-β-1,4-Xylanase I MoXYL1A Regulates Conidiation, Appressorium Maturation and Virulence of the Rice Blast Fungus
title_full_unstemmed Magnaporthe oryzae Chloroplast Targeting Endo-β-1,4-Xylanase I MoXYL1A Regulates Conidiation, Appressorium Maturation and Virulence of the Rice Blast Fungus
title_short Magnaporthe oryzae Chloroplast Targeting Endo-β-1,4-Xylanase I MoXYL1A Regulates Conidiation, Appressorium Maturation and Virulence of the Rice Blast Fungus
title_sort magnaporthe oryzae chloroplast targeting endo-β-1,4-xylanase i moxyl1a regulates conidiation, appressorium maturation and virulence of the rice blast fungus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374862/
https://www.ncbi.nlm.nih.gov/pubmed/35960402
http://dx.doi.org/10.1186/s12284-022-00584-2
work_keys_str_mv AT shabbirammarah magnaportheoryzaechloroplasttargetingendob14xylanaseimoxyl1aregulatesconidiationappressoriummaturationandvirulenceofthericeblastfungus
AT batoolwajjiha magnaportheoryzaechloroplasttargetingendob14xylanaseimoxyl1aregulatesconidiationappressoriummaturationandvirulenceofthericeblastfungus
AT yudan magnaportheoryzaechloroplasttargetingendob14xylanaseimoxyl1aregulatesconidiationappressoriummaturationandvirulenceofthericeblastfungus
AT linlili magnaportheoryzaechloroplasttargetingendob14xylanaseimoxyl1aregulatesconidiationappressoriummaturationandvirulenceofthericeblastfungus
AT anqiuli magnaportheoryzaechloroplasttargetingendob14xylanaseimoxyl1aregulatesconidiationappressoriummaturationandvirulenceofthericeblastfungus
AT xiaominchen magnaportheoryzaechloroplasttargetingendob14xylanaseimoxyl1aregulatesconidiationappressoriummaturationandvirulenceofthericeblastfungus
AT guohengyuan magnaportheoryzaechloroplasttargetingendob14xylanaseimoxyl1aregulatesconidiationappressoriummaturationandvirulenceofthericeblastfungus
AT yuanshuangshuang magnaportheoryzaechloroplasttargetingendob14xylanaseimoxyl1aregulatesconidiationappressoriummaturationandvirulenceofthericeblastfungus
AT malotasekete magnaportheoryzaechloroplasttargetingendob14xylanaseimoxyl1aregulatesconidiationappressoriummaturationandvirulenceofthericeblastfungus
AT wangzonghua magnaportheoryzaechloroplasttargetingendob14xylanaseimoxyl1aregulatesconidiationappressoriummaturationandvirulenceofthericeblastfungus
AT norvienyekujustice magnaportheoryzaechloroplasttargetingendob14xylanaseimoxyl1aregulatesconidiationappressoriummaturationandvirulenceofthericeblastfungus