Mamarabadi Mojtaba, Jensen Birgit, Jensen Dan Funck, Lübeck Mette
Plant Pathology Section, Department of Plant Biology, Faculty of Life Sciences, University of Copenhagen, Copenhagen, Denmark.
FEMS Microbiol Lett. 2008 Aug;285(1):101-10. doi: 10.1111/j.1574-6968.2008.01228.x. Epub 2008 Jun 28.
Clonostachys rosea is a well-known biocontrol agent against Botrytis cinerea, the causal agent of gray mold in strawberry. The activity of cell wall-degrading enzymes might play a significant role for successful biocontrol by C. rosea. The expression pattern of four chitinases, and two endoglucanase genes from C. rosea strain IK726 was analyzed using real-time RT-PCR in vitro and in strawberry leaves during interaction with B. cinerea. Specific primers were designed for beta-tubulin genes from C. rosea and B. cinerea, respectively, and a gene encoding a DNA-binding protein (DBP) from strawberry, allowing in situ activity assessment of each fungus in vitro and during their interaction on strawberry leaves. Growth of B. cinerea was inhibited in all pathogen-antagonist interactions while the activity of IK726 was slightly increased. In all in vitro interactions, four of the six genes were upregulated while no change in expression of two endochitinases was measured. In strawberry leaves, the chitinase genes were upregulated 2-12-fold, except one of the endochitinases, whereas no change in expression of the two endoglucanases was measured. The results suggest that three out of four chitinase genes of IK726 are involved in biocontrol on leaves. This is the first example of monitoring of expression of chitinolytic genes in interactions between biocontrol agents and pathogens in plant material.
粉红粘帚霉是一种著名的防治灰葡萄孢的生防菌,灰葡萄孢是草莓灰霉病的病原菌。细胞壁降解酶的活性可能在粉红粘帚霉成功进行生物防治中发挥重要作用。利用实时逆转录聚合酶链反应(RT-PCR),在体外以及在与灰葡萄孢相互作用的草莓叶片中,分析了粉红粘帚霉菌株IK726的四种几丁质酶和两种内切葡聚糖酶基因的表达模式。分别为粉红粘帚霉和灰葡萄孢的β-微管蛋白基因以及草莓中一种编码DNA结合蛋白(DBP)的基因设计了特异性引物,从而能够在体外以及它们在草莓叶片上相互作用期间对每种真菌进行原位活性评估。在所有病原菌与拮抗菌的相互作用中,灰葡萄孢的生长均受到抑制,而IK726的活性略有增加。在所有体外相互作用中,六个基因中的四个基因表达上调,而两种内切几丁质酶的表达未检测到变化。在草莓叶片中,除一种内切几丁质酶外,几丁质酶基因表达上调了2至12倍,而两种内切葡聚糖酶的表达未检测到变化。结果表明,IK726的四个几丁质酶基因中有三个参与叶片上的生物防治。这是在植物材料中监测生防菌与病原菌相互作用期间几丁质分解基因表达的首个实例。