Actin-bundling protein fimbrin regulates pathogenicity via organizing F-actin dynamics during appressorium development in Colletotrichum gloeosporioides

被引:16
|
作者
Zhang, Yi [1 ,2 ]
An, Bang [1 ,2 ]
Wang, Wenfeng [1 ]
Zhang, Bei [1 ,2 ]
He, Chaozu [1 ,2 ]
Luo, Hongli [1 ,2 ]
Wang, Qiannan [1 ,2 ]
机构
[1] Hainan Univ, Coll Trop Crops, Hainan Key Lab Sustainable Utilizat Trop Bioresou, Key Lab Biotechnol Salt Tolerant Crops Hainan Pro, Haikou 570228, Hainan, Peoples R China
[2] Hainan Univ, Hainan Yazhou Bay Seed Lab, Sanya Nanfan Res Inst, Sanya, Peoples R China
基金
中国国家自然科学基金;
关键词
actin cytoskeleton; appressorium; Colletotrichum gloeosporioides; fimbrin; pore; septin; RICE BLAST FUNGUS; PLANT INFECTION; GROWTH; CYTOSKELETON; LOCALIZATION; POLARIZATION; CYTOKINESIS; ENDOCYTOSIS; BIOLOGY; MELANIN;
D O I
10.1111/mpp.13242
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Anthracnose caused by Colletotrichum gloeosporioides leads to serious economic loss to rubber tree yield and other tropical crops. The appressorium, a specialized dome-shaped infection structure, plays a crucial role in the pathogenesis of C. gloeosporioides. However, the mechanism of how actin cytoskeleton dynamics regulate appressorium formation and penetration remains poorly defined in C. gloeosporioides. In this study, an actin cross-linking protein fimbrin homologue (CgFim1) was identified in C. gloeosporioides, and the knockout of CgFim1 led to impairment in vegetative growth, conidiation, and pathogenicity. We then investigated the roles of CgFim1 in the dynamic organization of the actin cytoskeleton. We observed that actin patches and cables localized at the apical and subapical regions of the hyphal tip, and showed a disc-to-ring dynamic around the pore during appressorium development. CgFim1 showed a similar distribution pattern to the actin cytoskeleton. Moreover, knockout of CgFim1 affected the polarity of the actin cytoskeleton in the hyphal tip and disrupted the actin dynamics and ring structure formation in the appressorium, which prevented polar growth and appressorium development. The CgFim1 mutant also interfered with the septin structure formation. This caused defects in pore wall overlay formation, pore contraction, and the extension of the penetration peg. These results reveal the mechanism by which CgFim1 regulates the growth and pathogenicity of C. gloeosporioides by organizing the actin cytoskeleton.
引用
收藏
页码:1472 / 1486
页数:15
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