Cargando…

The Photoreceptor Components FaWC1 and FaWC2 of Fusarium asiaticum Cooperatively Regulate Light Responses but Play Independent Roles in Virulence Expression

Fusarium asiaticum belongs to one of the phylogenetical subgroups of the F. graminearum species complex and is epidemically predominant in the East Asia area. The life cycle of F. asiaticum is significantly regulated by light. In this study, the fungal blue light receptor white collar complex (WCC),...

Descripción completa

Detalles Bibliográficos
Autores principales: Tang, Ying, Zhu, Pinkuan, Lu, Zhengyu, Qu, Yao, Huang, Li, Zheng, Ni, Wang, Yiwen, Nie, Haozhen, Jiang, Yina, Xu, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7143034/
https://www.ncbi.nlm.nih.gov/pubmed/32150839
http://dx.doi.org/10.3390/microorganisms8030365
_version_ 1783519519948406784
author Tang, Ying
Zhu, Pinkuan
Lu, Zhengyu
Qu, Yao
Huang, Li
Zheng, Ni
Wang, Yiwen
Nie, Haozhen
Jiang, Yina
Xu, Ling
author_facet Tang, Ying
Zhu, Pinkuan
Lu, Zhengyu
Qu, Yao
Huang, Li
Zheng, Ni
Wang, Yiwen
Nie, Haozhen
Jiang, Yina
Xu, Ling
author_sort Tang, Ying
collection PubMed
description Fusarium asiaticum belongs to one of the phylogenetical subgroups of the F. graminearum species complex and is epidemically predominant in the East Asia area. The life cycle of F. asiaticum is significantly regulated by light. In this study, the fungal blue light receptor white collar complex (WCC), including FaWC1 and FaWC2, were characterized in F. asiaticum. The knockout mutants ΔFawc1 and ΔFawc2 were generated by replacing the target genes via homologous recombination events. The two mutants showed similar defects in light-induced carotenoid biosynthesis, UV-C resistance, sexual fruiting body development, and the expression of the light-responsive marker genes, while in contrast, all these light responses were characteristics in wild-type (WT) and their complementation strains, indicating that FaWC1 and FaWC2 are involved in the light sensing of F. asiaticum. Unexpectedly, however, the functions of Fawc1 and Fawc2 diverged in regulating virulence, as the ΔFawc1 was avirulent to the tested host plant materials, but ΔFawc2 was equivalent to WT in virulence. Moreover, functional analysis of FaWC1 by partial disruption revealed that its light–oxygen–voltage (LOV) domain was required for light sensing but dispensable for virulence, and its Zinc-finger domain was required for virulence expression but not for light signal transduction. Collectively, these results suggest that the conserved fungal blue light receptor WCC not only endows F. asiaticum with light-sensing ability to achieve adaptation to environment, but it also regulates virulence expression by the individual component FaWC1 in a light-independent manner, and the latter function opens a way for investigating the pathogenicity mechanisms of this important crop disease agent.
format Online
Article
Text
id pubmed-7143034
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-71430342020-04-14 The Photoreceptor Components FaWC1 and FaWC2 of Fusarium asiaticum Cooperatively Regulate Light Responses but Play Independent Roles in Virulence Expression Tang, Ying Zhu, Pinkuan Lu, Zhengyu Qu, Yao Huang, Li Zheng, Ni Wang, Yiwen Nie, Haozhen Jiang, Yina Xu, Ling Microorganisms Article Fusarium asiaticum belongs to one of the phylogenetical subgroups of the F. graminearum species complex and is epidemically predominant in the East Asia area. The life cycle of F. asiaticum is significantly regulated by light. In this study, the fungal blue light receptor white collar complex (WCC), including FaWC1 and FaWC2, were characterized in F. asiaticum. The knockout mutants ΔFawc1 and ΔFawc2 were generated by replacing the target genes via homologous recombination events. The two mutants showed similar defects in light-induced carotenoid biosynthesis, UV-C resistance, sexual fruiting body development, and the expression of the light-responsive marker genes, while in contrast, all these light responses were characteristics in wild-type (WT) and their complementation strains, indicating that FaWC1 and FaWC2 are involved in the light sensing of F. asiaticum. Unexpectedly, however, the functions of Fawc1 and Fawc2 diverged in regulating virulence, as the ΔFawc1 was avirulent to the tested host plant materials, but ΔFawc2 was equivalent to WT in virulence. Moreover, functional analysis of FaWC1 by partial disruption revealed that its light–oxygen–voltage (LOV) domain was required for light sensing but dispensable for virulence, and its Zinc-finger domain was required for virulence expression but not for light signal transduction. Collectively, these results suggest that the conserved fungal blue light receptor WCC not only endows F. asiaticum with light-sensing ability to achieve adaptation to environment, but it also regulates virulence expression by the individual component FaWC1 in a light-independent manner, and the latter function opens a way for investigating the pathogenicity mechanisms of this important crop disease agent. MDPI 2020-03-05 /pmc/articles/PMC7143034/ /pubmed/32150839 http://dx.doi.org/10.3390/microorganisms8030365 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tang, Ying
Zhu, Pinkuan
Lu, Zhengyu
Qu, Yao
Huang, Li
Zheng, Ni
Wang, Yiwen
Nie, Haozhen
Jiang, Yina
Xu, Ling
The Photoreceptor Components FaWC1 and FaWC2 of Fusarium asiaticum Cooperatively Regulate Light Responses but Play Independent Roles in Virulence Expression
title The Photoreceptor Components FaWC1 and FaWC2 of Fusarium asiaticum Cooperatively Regulate Light Responses but Play Independent Roles in Virulence Expression
title_full The Photoreceptor Components FaWC1 and FaWC2 of Fusarium asiaticum Cooperatively Regulate Light Responses but Play Independent Roles in Virulence Expression
title_fullStr The Photoreceptor Components FaWC1 and FaWC2 of Fusarium asiaticum Cooperatively Regulate Light Responses but Play Independent Roles in Virulence Expression
title_full_unstemmed The Photoreceptor Components FaWC1 and FaWC2 of Fusarium asiaticum Cooperatively Regulate Light Responses but Play Independent Roles in Virulence Expression
title_short The Photoreceptor Components FaWC1 and FaWC2 of Fusarium asiaticum Cooperatively Regulate Light Responses but Play Independent Roles in Virulence Expression
title_sort photoreceptor components fawc1 and fawc2 of fusarium asiaticum cooperatively regulate light responses but play independent roles in virulence expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7143034/
https://www.ncbi.nlm.nih.gov/pubmed/32150839
http://dx.doi.org/10.3390/microorganisms8030365
work_keys_str_mv AT tangying thephotoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT zhupinkuan thephotoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT luzhengyu thephotoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT quyao thephotoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT huangli thephotoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT zhengni thephotoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT wangyiwen thephotoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT niehaozhen thephotoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT jiangyina thephotoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT xuling thephotoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT tangying photoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT zhupinkuan photoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT luzhengyu photoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT quyao photoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT huangli photoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT zhengni photoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT wangyiwen photoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT niehaozhen photoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT jiangyina photoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression
AT xuling photoreceptorcomponentsfawc1andfawc2offusariumasiaticumcooperativelyregulatelightresponsesbutplayindependentrolesinvirulenceexpression