College of Biology and Pharmaceutical Engineering, Wuhan Polytechnic University, Wuhan 430023, People's Republic of China.
Hubei Academy of Forestry, Wuhan 430075, People's Republic of China.
Plant Sci. 2019 Jun;283:1-10. doi: 10.1016/j.plantsci.2019.02.012. Epub 2019 Feb 27.
Colletotrichum higginsianum causes anthracnose disease in a wide range of cruciferous crops and has been used as a model system to study plant-pathogen interactions and pathogenicity of hemibiotrophic plant pathogens. Conidiation, hyphae growth, appressorial development and appressorial penetration are significant steps during the infection process of C. higginsianum. However, the mechanisms of these important steps during infection remain incompletely understood. To further investigate the mechanisms of the plant-C. higginsianum interactions during infection progress, we characterized Cyclase-Associated Protein (ChCAP) gene. Deletion of the ChCAP gene resulted in reduction in conidiation and hyphal growth rate. The pathogenicity of ΔChCAP mutants was significantly reduced with much smaller lesion on the infected leaves compared to that of wild type strain with typically water-soaked and dark necrotic lesions on Arabidopsis leaves. Further study demonstrated that the appressorial formation rate, turgor pressure, penetration ability and switch from biotrophic to necrotrophic phases decreased obviously in ΔChCAP mutants, indicating that the attenuated pathogenicity of ΔChCAP mutants was due to these defective phenotypes. In addition, the ΔChCAP mutants sectored on PDA with abnormal, dark color, vesicle-like colony morphology and hyphae tip. Moreover, the ΔChCAP mutants had a reduced intracellular cAMP levels and exogenous cAMP can partially rescue the defects of ΔChCAP mutants in appressorial formation and penetration rate, but not in colony morphology, conidial shape and virulence, indicating that ChCAP is a key component in cAMP signaling pathway and likely play other roles in biology of C. higginsianum. In summary, our findings support the role of ChCAP in regulating conidiation, intracellular cAMP level, hyphal growth, appressorial formation, penetration ability and pathogenicity of this hemibiotrophic fungus.
密旋腔菌引起广泛的十字花科作物炭疽病,已被用作研究植物-病原体相互作用和半活体病原体致病性的模式系统。分生孢子形成、菌丝生长、附着胞发育和附着胞穿透是密旋腔菌感染过程中的重要步骤。然而,这些感染过程中的重要步骤的机制仍不完全清楚。为了进一步研究感染过程中植物-密旋腔菌相互作用的机制,我们对环化酶相关蛋白(ChCAP)基因进行了特征描述。ChCAP 基因缺失导致分生孢子形成和菌丝生长速度降低。与野生型菌株相比,ΔChCAP 突变体的致病性显著降低,感染叶片上的病斑更小,典型的病斑表现为水渍状和暗褐色坏死。进一步的研究表明,ΔChCAP 突变体的附着胞形成率、膨压、穿透能力以及从活体营养阶段向坏死营养阶段的转变明显降低,表明 ΔChCAP 突变体的减弱致病性是由于这些缺陷表型所致。此外,ΔChCAP 突变体在 PDA 上出现了扇形,表现出异常的、深颜色的、囊泡样的菌落形态和菌丝尖端。此外,ΔChCAP 突变体的细胞内 cAMP 水平降低,外源性 cAMP 可以部分挽救 ΔChCAP 突变体在附着胞形成和穿透率方面的缺陷,但不能挽救菌落形态、分生孢子形状和毒力方面的缺陷,表明 ChCAP 是 cAMP 信号通路的关键组成部分,可能在密旋腔菌的生物学中发挥其他作用。总之,我们的研究结果支持 ChCAP 在调节半活体真菌的分生孢子形成、细胞内 cAMP 水平、菌丝生长、附着胞形成、穿透能力和致病性方面的作用。