Diao Yufei, Jin Jiyang, Xiong Xiong, Yu Chengming, Tian Yehan, Li Duochuan, Liu Huixiang
Shandong Research Center for Forestry Harmful Biological Control Engineering and Technology, College of Plant Protection, Shandong Agricultural University, Tai'an 271018, China.
Mountain Tai Forest Ecosystem Research Station of State Forestry Administration, Forestry College, Shandong Agricultural University, Tai'an 271018, China.
J Fungi (Basel). 2023 Jun 20;9(6):692. doi: 10.3390/jof9060692.
Apple canker disease, caused by , is one of the most serious apple tree diseases in China. is an important transcription factor that acts on the cyclic adenosine signaling pathway (cAMP/PKA), regulating the growth, development, morphological differentiation, and pathogenic forces of the pathogen. We perform transcriptome analysis of the deletion mutant and the wild-type strain 11-175 and identify a significantly differentially expressed gene, , a zinc finger motif transcription factor in . In this study, we obtain the gene using the single deletion mutant via homologous recombination. To determine the relationship between and , we also obtain a double deletion mutant . Compared to the wild-type strain 11-175, the single deletion mutant shows a drastic reduction in growth rate and forms more pycnidia on the PDA medium. Additionally, the growth of the mutant is inhibited by SDS, Congo red, and fluorescent brighteners. In comparison to the single deletion mutant , the double deletion mutant shows no significant change in growth or conidiation and is unable to produce conidia. The growth rate is significantly increased in Congo red, NaCl, and Sorbitol mediums. These results demonstrate that plays important roles in growth, pathogenicity, asexual development, and maintenance of cell wall integrity. can recover osmotic stress and cell wall integrity defects caused by the deletion of , as well as restore the loss of pathogenicity caused by the deletion of the gene, but not completely.
苹果溃疡病由……引起,是中国最严重的苹果树病害之一。……是一种重要的转录因子,作用于环腺苷信号通路(cAMP/PKA),调节病原菌的生长、发育、形态分化和致病力。我们对……缺失突变体和野生型菌株11 - 175进行了转录组分析,鉴定出一个显著差异表达的基因……,它是……中的一个锌指基序转录因子。在本研究中,我们通过同源重组利用单缺失突变体获得了……基因。为了确定……与……之间的关系,我们还获得了双缺失突变体……。与野生型菌株11 - 175相比,单缺失突变体……的生长速率急剧下降,并且在PDA培养基上形成更多的分生孢子器。此外,该突变体的生长受到SDS、刚果红和荧光增白剂的抑制。与单缺失突变体……相比,双缺失突变体……在生长或产孢方面没有显著变化,并且无法产生分生孢子。在刚果红、NaCl和山梨醇培养基中生长速率显著增加。这些结果表明……在生长、致病性、无性发育和细胞壁完整性维持中起重要作用。……可以恢复由……缺失引起的渗透胁迫和细胞壁完整性缺陷,以及恢复由……基因缺失导致的致病性丧失,但不能完全恢复。