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Loss of function of VdDrs2, a P4-ATPase, impairs the toxin secretion and microsclerotia formation, and decreases the pathogenicity of Verticillium dahliae
Four P4-ATPase flippase genes, VdDrs2, VdNeo1, VdP4-4, and VdDnf1 were identified in Verticillium dahliae, one of the most devastating phytopathogenic fungi in the world. Knock out of VdDrs2, VdNeo1, and VdP4-4, or knock down of VdDnf1 significantly decreased the pathogenicity of the mutants in cott...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443849/ https://www.ncbi.nlm.nih.gov/pubmed/36072318 http://dx.doi.org/10.3389/fpls.2022.944364 |
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author | Ren, Hui Li, Xianbi Li, Yujie Li, Mengjun Sun, Jiyuan Wang, Fanlong Zeng, Jianyan Chen, Yang Wang, Lei Yan, Xingying Fan, Yanhua Jin, Dan Pei, Yan |
author_facet | Ren, Hui Li, Xianbi Li, Yujie Li, Mengjun Sun, Jiyuan Wang, Fanlong Zeng, Jianyan Chen, Yang Wang, Lei Yan, Xingying Fan, Yanhua Jin, Dan Pei, Yan |
author_sort | Ren, Hui |
collection | PubMed |
description | Four P4-ATPase flippase genes, VdDrs2, VdNeo1, VdP4-4, and VdDnf1 were identified in Verticillium dahliae, one of the most devastating phytopathogenic fungi in the world. Knock out of VdDrs2, VdNeo1, and VdP4-4, or knock down of VdDnf1 significantly decreased the pathogenicity of the mutants in cotton. Among the mutants, the greatest decrease in pathogenicity was observed in ΔVdDrs2. VdDrs2 was localized to plasma membrane, vacuoles, and trans-Golgi network (TGN). In vivo observation showed that the infection of the cotton by ΔVdDrs2 was significantly delayed. The amount of two known Verticillium toxins, sulfacetamide, and fumonisin B1 in the fermentation broth produced by the ΔVdDrs2 strain was significantly reduced, and the toxicity of the crude Verticillium wilt toxins to cotton cells was attenuated. In addition, the defect of VdDrs2 impaired the synthesis of melanin and the formation of microsclerotia, and decreased the sporulation of V. dahliae. Our data indicate a key role of P4 ATPases-associated vesicle transport in toxin secretion of disease fungi and support the importance of mycotoxins in the pathogenicity of V. dahliae. |
format | Online Article Text |
id | pubmed-9443849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94438492022-09-06 Loss of function of VdDrs2, a P4-ATPase, impairs the toxin secretion and microsclerotia formation, and decreases the pathogenicity of Verticillium dahliae Ren, Hui Li, Xianbi Li, Yujie Li, Mengjun Sun, Jiyuan Wang, Fanlong Zeng, Jianyan Chen, Yang Wang, Lei Yan, Xingying Fan, Yanhua Jin, Dan Pei, Yan Front Plant Sci Plant Science Four P4-ATPase flippase genes, VdDrs2, VdNeo1, VdP4-4, and VdDnf1 were identified in Verticillium dahliae, one of the most devastating phytopathogenic fungi in the world. Knock out of VdDrs2, VdNeo1, and VdP4-4, or knock down of VdDnf1 significantly decreased the pathogenicity of the mutants in cotton. Among the mutants, the greatest decrease in pathogenicity was observed in ΔVdDrs2. VdDrs2 was localized to plasma membrane, vacuoles, and trans-Golgi network (TGN). In vivo observation showed that the infection of the cotton by ΔVdDrs2 was significantly delayed. The amount of two known Verticillium toxins, sulfacetamide, and fumonisin B1 in the fermentation broth produced by the ΔVdDrs2 strain was significantly reduced, and the toxicity of the crude Verticillium wilt toxins to cotton cells was attenuated. In addition, the defect of VdDrs2 impaired the synthesis of melanin and the formation of microsclerotia, and decreased the sporulation of V. dahliae. Our data indicate a key role of P4 ATPases-associated vesicle transport in toxin secretion of disease fungi and support the importance of mycotoxins in the pathogenicity of V. dahliae. Frontiers Media S.A. 2022-08-22 /pmc/articles/PMC9443849/ /pubmed/36072318 http://dx.doi.org/10.3389/fpls.2022.944364 Text en Copyright © 2022 Ren, Li, Li, Li, Sun, Wang, Zeng, Chen, Wang, Yan, Fan, Jin and Pei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Ren, Hui Li, Xianbi Li, Yujie Li, Mengjun Sun, Jiyuan Wang, Fanlong Zeng, Jianyan Chen, Yang Wang, Lei Yan, Xingying Fan, Yanhua Jin, Dan Pei, Yan Loss of function of VdDrs2, a P4-ATPase, impairs the toxin secretion and microsclerotia formation, and decreases the pathogenicity of Verticillium dahliae |
title | Loss of function of VdDrs2, a P4-ATPase, impairs the toxin secretion and microsclerotia formation, and decreases the pathogenicity of Verticillium dahliae |
title_full | Loss of function of VdDrs2, a P4-ATPase, impairs the toxin secretion and microsclerotia formation, and decreases the pathogenicity of Verticillium dahliae |
title_fullStr | Loss of function of VdDrs2, a P4-ATPase, impairs the toxin secretion and microsclerotia formation, and decreases the pathogenicity of Verticillium dahliae |
title_full_unstemmed | Loss of function of VdDrs2, a P4-ATPase, impairs the toxin secretion and microsclerotia formation, and decreases the pathogenicity of Verticillium dahliae |
title_short | Loss of function of VdDrs2, a P4-ATPase, impairs the toxin secretion and microsclerotia formation, and decreases the pathogenicity of Verticillium dahliae |
title_sort | loss of function of vddrs2, a p4-atpase, impairs the toxin secretion and microsclerotia formation, and decreases the pathogenicity of verticillium dahliae |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443849/ https://www.ncbi.nlm.nih.gov/pubmed/36072318 http://dx.doi.org/10.3389/fpls.2022.944364 |
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