Saeedizadeh Ayatollah, Kheiri Ahmad, Zad Javad, Etebarian Hasan Reza, Bandani Ali Reza, Sharifi Rouhollah
Dep. of Plant Protection, Shahed University, Tehran, Iran.
Commun Agric Appl Biol Sci. 2009;74(2):559-66.
Second stage juvenile (J2) of root-knot nematode, Meloidogyne javanica, and microsclerotia of verticilliosis, Verticillium dahliae, were used as the source of inoculum for nematode and fungus respectively. One-year-old seedlings of olive cultivar, Zard, Roghani, Koroneiki and Manzanilla, were transplanted to pots containing 2000g of sterilized sandy loam soil. Experiment was conducted in completely randomized design with 32 Treatments and five replications. Treatments were as follows: control, nematode alone, fungus alone and fungus+nematode. Pots were inoculated with (0, 2000, 3000, 4000) J2 of nematode and/or (10 no/g soil) microsclerotia of fungus according to the treatments. Quantitative activity of soluble proxidase, cell wall bounded proxidase, beta-1,3-glucanase and B-1,4-glucanase were determined by the pirocatechol, hydrogen proxide, guaiacol and laminarin-dinitrosalicylilate methods, respectively, on 1,10, 20 and 30 days after inoculation. Results showed that these enzymes in leaves and roots of seedlings inoculated with pathogens increased (p < or = 0/05). In this study changes of these enzymes as compared with nematode alone and fungus alone treatments were increased in fungus+nematode treatments in seedlings (p < or = 0/05). Maximum of quantitative changes of these enzymes were observed in fungus+nematode (4000J2) treatment on cv. Koroneiki. Based on the results obtained in this study, quantitative activity of these enzymes in olive roots and leaves were be more on cvs. Koroneiki, Roghani, Zard and Manzanilla, respectively (p < or = 0/05).
爪哇根结线虫的第二期幼虫(J2)和大丽轮枝菌的微菌核分别被用作线虫和真菌的接种源。将一年生的橄榄品种扎德、罗哈尼、科罗内基和曼萨尼拉的幼苗移植到装有2000克灭菌砂壤土的花盆中。实验采用完全随机设计,有32个处理,5次重复。处理如下:对照、单独接种线虫、单独接种真菌以及真菌+线虫。根据处理,花盆接种(0、2000、3000、4000)条线虫J2和/或(10个/克土壤)真菌微菌核。分别在接种后1、10、20和30天,通过邻苯二酚、过氧化氢、愈创木酚和海带多糖-二硝基水杨酸法测定可溶性过氧化物酶、细胞壁结合过氧化物酶、β-1,3-葡聚糖酶和β-1,4-葡聚糖酶的定量活性。结果表明,接种病原体的幼苗叶片和根部中的这些酶活性增加(p≤0.05)。在本研究中,与单独接种线虫和单独接种真菌的处理相比,真菌+线虫处理的幼苗中这些酶的变化增加(p≤0.05)。在科罗内基品种的真菌+线虫(4000J2)处理中观察到这些酶的最大定量变化。根据本研究获得的结果,这些酶在橄榄根和叶中的定量活性在科罗内基、罗哈尼、扎德和曼萨尼拉品种中分别更高(p≤0.05)。