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The Bursaphelenchus xylophilus candidate effector BxLip‐3 targets the class I chitinases to suppress immunity in pine
Lipase is involved in lipid hydrolysis, which is related to nematodes' energy reserves and stress resistance. However, the role of lipases in Bursaphelenchus xylophilus, a notorious plant‐parasitic nematode responsible for severe damage to pine forest ecosystems, remains largely obscure. Here,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423331/ https://www.ncbi.nlm.nih.gov/pubmed/37448165 http://dx.doi.org/10.1111/mpp.13334 |
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author | Qiu, Yi‐Jun Wu, Xiao‐Qin Wen, Tong‐Yue Hu, Long‐Jiao Rui, Lin Zhang, Yan Ye, Jian‐Ren |
author_facet | Qiu, Yi‐Jun Wu, Xiao‐Qin Wen, Tong‐Yue Hu, Long‐Jiao Rui, Lin Zhang, Yan Ye, Jian‐Ren |
author_sort | Qiu, Yi‐Jun |
collection | PubMed |
description | Lipase is involved in lipid hydrolysis, which is related to nematodes' energy reserves and stress resistance. However, the role of lipases in Bursaphelenchus xylophilus, a notorious plant‐parasitic nematode responsible for severe damage to pine forest ecosystems, remains largely obscure. Here, we characterized a class III lipase as a candidate effector and named it BxLip‐3. It was transcriptionally up‐regulated in the parasitic stages of B. xylophilus and specifically expressed in the oesophageal gland cells and the intestine. In addition, BxLip‐3 suppressed cell death triggered by the pathogen‐associated molecular patterns PsXEG1 and BxCDP1 in Nicotiana benthamiana, and its Lipase‐3 domain is essential for immunosuppression. Silencing of the BxLip‐3 gene resulted in a delay in disease onset and increased the activity of antioxidant enzymes and the expression of pathogenesis‐related (PR) genes. Plant chitinases are thought to be PR proteins involved in the defence system against pathogen attack. Using yeast two‐hybrid and co‐immunoprecipitation assays, we identified two class I chitinases in Pinus thunbergii, PtChia1‐3 and PtChia1‐4, as targets of BxLip‐3. The expression of these two chitinases was up‐regulated during B. xylophilus inoculation and inhibited by BxLip‐3. Overall, this study illustrated that BxLip‐3 is a crucial virulence factor that plays a critical role in the interaction between B. xylophilus and host pine. |
format | Online Article Text |
id | pubmed-10423331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104233312023-08-14 The Bursaphelenchus xylophilus candidate effector BxLip‐3 targets the class I chitinases to suppress immunity in pine Qiu, Yi‐Jun Wu, Xiao‐Qin Wen, Tong‐Yue Hu, Long‐Jiao Rui, Lin Zhang, Yan Ye, Jian‐Ren Mol Plant Pathol Original Articles Lipase is involved in lipid hydrolysis, which is related to nematodes' energy reserves and stress resistance. However, the role of lipases in Bursaphelenchus xylophilus, a notorious plant‐parasitic nematode responsible for severe damage to pine forest ecosystems, remains largely obscure. Here, we characterized a class III lipase as a candidate effector and named it BxLip‐3. It was transcriptionally up‐regulated in the parasitic stages of B. xylophilus and specifically expressed in the oesophageal gland cells and the intestine. In addition, BxLip‐3 suppressed cell death triggered by the pathogen‐associated molecular patterns PsXEG1 and BxCDP1 in Nicotiana benthamiana, and its Lipase‐3 domain is essential for immunosuppression. Silencing of the BxLip‐3 gene resulted in a delay in disease onset and increased the activity of antioxidant enzymes and the expression of pathogenesis‐related (PR) genes. Plant chitinases are thought to be PR proteins involved in the defence system against pathogen attack. Using yeast two‐hybrid and co‐immunoprecipitation assays, we identified two class I chitinases in Pinus thunbergii, PtChia1‐3 and PtChia1‐4, as targets of BxLip‐3. The expression of these two chitinases was up‐regulated during B. xylophilus inoculation and inhibited by BxLip‐3. Overall, this study illustrated that BxLip‐3 is a crucial virulence factor that plays a critical role in the interaction between B. xylophilus and host pine. John Wiley and Sons Inc. 2023-07-13 /pmc/articles/PMC10423331/ /pubmed/37448165 http://dx.doi.org/10.1111/mpp.13334 Text en © 2023 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Qiu, Yi‐Jun Wu, Xiao‐Qin Wen, Tong‐Yue Hu, Long‐Jiao Rui, Lin Zhang, Yan Ye, Jian‐Ren The Bursaphelenchus xylophilus candidate effector BxLip‐3 targets the class I chitinases to suppress immunity in pine |
title | The Bursaphelenchus xylophilus candidate effector BxLip‐3 targets the class I chitinases to suppress immunity in pine |
title_full | The Bursaphelenchus xylophilus candidate effector BxLip‐3 targets the class I chitinases to suppress immunity in pine |
title_fullStr | The Bursaphelenchus xylophilus candidate effector BxLip‐3 targets the class I chitinases to suppress immunity in pine |
title_full_unstemmed | The Bursaphelenchus xylophilus candidate effector BxLip‐3 targets the class I chitinases to suppress immunity in pine |
title_short | The Bursaphelenchus xylophilus candidate effector BxLip‐3 targets the class I chitinases to suppress immunity in pine |
title_sort | bursaphelenchus xylophilus candidate effector bxlip‐3 targets the class i chitinases to suppress immunity in pine |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423331/ https://www.ncbi.nlm.nih.gov/pubmed/37448165 http://dx.doi.org/10.1111/mpp.13334 |
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