Department of Plant Pathology, Agricultural Research Organization, Gilat Research Center, MP Negev 85280, Israel.
Mol Plant Pathol. 2012 Feb;13(2):187-97. doi: 10.1111/j.1364-3703.2011.00740.x. Epub 2011 Aug 17.
Colletotrichum coccodes (Wallr.) S. Hughes, the causal agent of black dot on potato and anthracnose on tomato, reduces yield and crop quality. We explored the role of secreted pectate lyase (PL), a cell wall-degrading enzyme, in the aggressiveness of C. coccodes. In vitro-cultivated highly aggressive isolates secreted immunologically detectable PL levels 6 h after transfer to secondary medium versus 12 h for mildly aggressive isolates, suggesting that secreted PL is a virulence factor. The gene encoding PL, CcpelA, was cloned and used for the genetic manipulation of highly (US-41 and Si-72) and mildly (Si-60) aggressive isolates. CcpelA gene-disrupted mutants showed reduced aggressiveness towards tomato fruits and impaired PL secretion and extracellular activity. Conversely, overexpression of CcpelA in the Si-60 isolate increased its aggressiveness and PL secretion. Comparison of CcpelA cloned from isolates US-41 and Si-60 revealed that both encode identical proteins, but differ in their promoters. Bioinformatics analysis for cis-acting elements suggested that the promoters of the US-41 and Si-60 isolates contain one and no AreA-binding site (GATA box), respectively. AreA has been suggested to be involved in fungal aggressiveness; therefore, CcpelA may be a key virulence factor in C. coccodes pathogenicity, and the differences in isolate aggressiveness might result from promoter activity. Quantitative reverse transcriptase-polymerase chain reaction analyses confirmed the higher level of CcpelA transcript in isolate US-41 versus Si-60.
胶孢炭疽菌(Wallr.)S. Hughes 是导致马铃薯黑斑病和番茄炭疽病的病原菌,它会降低作物产量和品质。我们探索了分泌果胶裂解酶(PL)在胶孢炭疽菌侵袭性中的作用,这种酶是一种细胞壁降解酶。与侵袭性较弱的菌株相比,在体外培养的高度侵袭性菌株转移到次级培养基后 6 小时即可分泌可检测到的免疫 PL 水平,而侵袭性较弱的菌株则需要 12 小时,这表明分泌的 PL 是一种毒力因子。PL 编码基因 CcpelA 被克隆,并用于高度侵袭性(US-41 和 Si-72)和轻度侵袭性(Si-60)菌株的遗传操作。CcpelA 基因敲除突变体对番茄果实的侵袭性降低,PL 分泌和细胞外活性受损。相反,在 Si-60 菌株中过表达 CcpelA 增加了其侵袭性和 PL 分泌。从 US-41 和 Si-60 分离株克隆的 CcpelA 比较表明,它们编码的蛋白完全相同,但启动子不同。顺式作用元件的生物信息学分析表明,US-41 和 Si-60 分离株的启动子分别含有一个和没有 AreA 结合位点(GATA 盒)。已提出 AreA 参与真菌侵袭性;因此,CcpelA 可能是胶孢炭疽菌致病性的关键毒力因子,分离株侵袭性的差异可能源于启动子活性。定量逆转录聚合酶链反应分析证实,与 Si-60 分离株相比,US-41 分离株的 CcpelA 转录本水平更高。