Kalha C S, Gupta V, Gupta D, Priya Satya
Division of Plant Pathology, Sher-E-Kashmir University of Agricultural Sciences and Technology-Jammu, Udheywalla Campus, Jammu and Kashmir, 180002-India.
Department of Extension, Birsa Agricultural University, Ranchi-India.
Plant Dis. 2007 Sep;91(9):1203. doi: 10.1094/PDIS-91-9-1203B.
Saffron (Crocus sativus L.) is highly desirable as a condiment and is also used for medicinal purposes. In India, saffron is cultivated in 2,825 ha with a production of 6,048 t and an average yield of 2.28 kg/ha. Approximately 70 to 80% of the saffron crop in 25 commercial fields in the Kishtwar District of Jammu and Kashmir, India was affected with a corm rot from October 2005 to 2006. In newly infested fields, the disease occurred in small patches that gradually enlarged each year. Symptoms appeared as brown-to-dark brown sunken, irregular patches below corm scales. Lesions were usually 1 mm deep with raised margins. Severely infected corms had foliage that dried from the tip downward. White fungal mycelia appeared on the bulbs that rotted at later stages of disease development. Sclerotia formation was observed. For isolation of the pathogen, small bits of the infected tissue were surface sterilized in 0.1% mercuric chloride and washed three times in sterile distilled water. The surface-sterilized pieces were placed aseptically on potato dextrose agar and incubated at 28 ± 1°C for 3 days. The fungus was characterized by hard, brown-to-black sclerotia that was 1 to 2.1 mm in diameter with a pseudoparenchymatous rind. These were produced on sterile, cottony white mycelium with clamp connections. On the basis of morphological characteristics (3), the fungus was identified and deposited as Sclerotium rolfsii Sacc. at the Indian Type Culture Collection Center, IARI-New Delhi as ID No. 6491.07. Pathogenicity tests were carried out in a growth chamber maintained at 28 ± 1°C. S. rolfsii was grown in potato dextrose broth for 7 days and then blended to make a mycelial suspension. Fifty milliliters (1 × 10 hyphal fragments per ml) of the suspension was mixed in each kilogram of sterilized soil and placed in pots. Healthy saffron corms were planted in 10 pots containing soil infested with S. rolfsii, and five pots with noninfested soil served as controls. Symptoms appeared on eight corms 9 to 10 days after planting. Signs of the pathogen in the form of mycelia and sclerotia were also present. The corms rotted and died 12 to 14 days after inoculation. Control plants did not display any symptoms. S. rolfsii was reisolated from infected bulbs, thus proving Koch's postulates. Corm rot caused by Fusarium spp., Penicillium spp., and Rhizoctonia spp. is also reported on saffron (2). Fusarium oxysporum f. sp. gladioli has been reported in Italy (1). To our knowledge, this is the first report of S. rolfsii as being pathogenic on saffron from India. References: (1) P. Di Primo and C. Cappelli. Plant Dis. 84:806, 2000. (2) M. G. Hassan and L. Sobita Devi. Indian Phytopathol. 56:122, 2003. (3) Z. K. Punja and A. Damiani. Mycologia 88:694, 1996.
藏红花(番红花)作为一种调味品备受青睐,同时也用于药用。在印度,藏红花种植面积为2825公顷,产量为6048吨,平均产量为2.28千克/公顷。2005年10月至2006年期间,印度查谟和克什米尔基什特瓦尔区25个商业种植地中约70%至80%的藏红花作物受到球茎腐烂病的影响。在新受侵染的田地中,病害最初呈小斑块状出现,且每年逐渐扩大。症状表现为球茎鳞片下方出现褐色至深褐色的凹陷、不规则斑块。病斑通常深1毫米,边缘隆起。严重感染的球茎其叶片从尖端向下干枯。在病害发展后期腐烂的球茎上出现白色真菌菌丝体。观察到菌核的形成。为分离病原菌,将感染组织的小块在0.1%氯化汞中进行表面消毒,并在无菌蒸馏水中洗涤三次。将表面消毒后的组织块无菌接种到马铃薯葡萄糖琼脂培养基上,在28±1°C下培养3天。该真菌的特征是形成坚硬的、直径为1至2.1毫米的褐色至黑色菌核,菌核具有拟薄壁组织外皮。菌核在带有锁状联合的无菌、棉絮状白色菌丝体上产生。根据形态学特征(3),该真菌被鉴定为齐整小核菌,并作为编号为6491.07的菌株保藏于印度新德里国际农业研究机构(IARI)的印度模式培养物保藏中心。致病性试验在温度保持在28±1°C的生长室中进行。齐整小核菌在马铃薯葡萄糖肉汤中培养7天,然后搅拌制成菌丝体悬浮液。将50毫升(每毫升含1×10个菌丝片段)悬浮液与每千克灭菌土壤混合,放入花盆中。将健康的藏红花球茎种植在10个装有被齐整小核菌侵染土壤的花盆中,5个装有未侵染土壤的花盆作为对照。种植后9至10天,8个球茎出现症状。同时也出现了病原菌以菌丝体和菌核形式存在的迹象。接种后12至14天,球茎腐烂死亡。对照植株未表现出任何症状。从感染的球茎中再次分离出齐整小核菌,从而证实了柯赫氏法则。据报道,尖孢镰刀菌、青霉菌和丝核菌也会引起藏红花球茎腐烂(2)。在意大利曾报道过唐菖蒲尖孢镰刀菌(1)。据我们所知,这是关于齐整小核菌对印度藏红花具有致病性的首次报道。参考文献:(1)P. Di Primo和C. Cappelli。《植物病害》84:806,2000。(2)M. G. Hassan和L. Sobita Devi。《印度植物病理学》56:122,2003。(3)Z. K. Punja和A. Damiani。《真菌学》88:694,1996。