Garibaldi A, Bertetti D, Gullino M L
Center of Competence AGROINNOVA, University of Torino, Via Leonardo da Vinci, 44, 10095 Grugliasco, Italy.
Plant Dis. 2006 Oct;90(10):1361. doi: 10.1094/PD-90-1361C.
Madagascar periwinkle (Catharanthus roseus), a plant belonging to the Apocynaceae family, is used for parks and gardens and sometimes grown in pots. At the end of the summer of 2005, a leaf blight was observed on plants in a public park of Torino. Semicircular, water-soaked lesions developed on leaves just above the soil line at the leaf-petiole junction and later along the leaf margins. Lesions expanded for several days along the midvein until the entire leaf was destroyed. Blighted leaves turned brown, withered, clung to the shoots, and matted on the surrounding foliage. Although lesions were not seen on the stem, affected plants often died leaving wide empty areas. Mycelia of the pathogen were often seen on and suspended between the leaves. Blight progressed from the leaves to the shoot tip. The diseased tissue was disinfected for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 μg/l streptomycin sulphate. A fungus with the morphological characters of Rhizoctonia solani was consistently and readily isolated and maintained in pure culture after single-hyphal tipping (4). The isolates of R. solani obtained from affected plants were successfully anastomosed with tester isolate AG 1 (ATCC 58946). The hyphal diameter at the point of anastomosis was reduced, the anastomosis point was obvious, and cell death of adjacent cells was observed. These results are consistent with other reports on anastomosis reactions (2). Pairing was also made with AG 2, 3, 4, 5, 7, and 11, with no anastomoses observed between the isolates and testers. Sclerotia were subspheroid in shape and had a size of 1 mm, which indicated that this pathogen was in subgroup 1B (4). For pathogenicity tests, the inoculum of R. solani was prepared by growing the pathogen on PDA for 7 days. Plants of C. roseus were grown in 3-liter containers (2 plants per pot) on a steam disinfested substrate (peat/ pomix/pine bark/clay). Artificial inoculation was carried out on 7-day-old plants by placing numerous fragments of PDA cultures on the leaves of the plants. Plants inoculated with PDA alone served as control treatments. Three replicates were used. Plants were maintained in a glasshouse at 20 to 25°C. The first symptoms, similar to those observed in the public park, developed 5 days after inoculation, and R. solani was consistently reisolated from infected plants. Control plants remained healthy. The pathogenicity test was carried out twice with similar results. This is, to our knowledge, the first report of R. solani on periwinkle in Italy. The same disease was reported in India (1) and the United States (3). References: (1) R. Balasubramanian and K. S. Bhama. Indian Phytopathol. 30:556, 1977. (2) D. E. Carling. Grouping in Rhizoctonia solani by hyphal anastomosis reactions. Pages 37-47 in: Rhizoctonia Species: Taxonomy, Molecular Biology, Ecology, Pathology and Disease Control. B. Sneh et al., eds. Kluwer Academic Publishers, the Netherlands, 1996. (3) A. K. Hagan and J. M. Mullen Plant Dis. 77:1169, 1993. (4) B. Sneh et al. Identification of Rhizoctonia Species. The American Phytopathological Society, St Paul, MN, 1991.
长春花(Catharanthus roseus)是夹竹桃科植物,用于公园和花园,有时也盆栽种植。2005年夏末,在都灵的一个公共公园里,人们发现长春花植株出现了叶枯病。在叶片与叶柄连接处土壤线以上的叶片上,以及后来沿着叶缘,出现了半圆形的水渍状病斑。病斑沿着中脉扩展数天,直到整片叶子坏死。病叶变成褐色,枯萎,附着在嫩枝上,并与周围的叶子交织在一起。虽然茎上没有病斑,但受影响的植株常常死亡,留下大片空地。在叶片上及其之间常常能看到病原菌的菌丝体。叶枯病从叶片蔓延到嫩梢顶端。将病组织在1%次氯酸钠中消毒1分钟,然后接种到添加了100μg/l硫酸链霉素的马铃薯葡萄糖琼脂(PDA)上。通过单菌丝尖端分离法(4),始终能很容易地分离出具有立枯丝核菌形态特征的真菌,并在纯培养物中保存。从受影响植株上获得的立枯丝核菌分离物与测试分离物AG 1(ATCC 58946)成功融合。融合处的菌丝直径变细,融合点明显,且观察到相邻细胞死亡。这些结果与其他关于融合反应的报道一致(2)。还将其与AG 2、3、4、5、7和11进行配对,分离物与测试物之间未观察到融合现象。菌核呈近球形,大小为1mm,这表明该病原菌属于1B亚组(4)。为进行致病性测试,将立枯丝核菌接种物通过在PDA上培养7天来制备。长春花植株种植在3升容器(每盆2株)中,基质经过蒸汽消毒(泥炭/混合基质/松树皮/黏土)。在7日龄植株上进行人工接种,方法是将大量PDA培养物碎片放在植株叶片上。仅接种PDA的植株作为对照处理。设置3次重复。植株置于20至25°C的温室中。接种5天后出现了与在公共公园中观察到的相似的最初症状,并且始终能从受感染植株上重新分离出立枯丝核菌。对照植株保持健康。致病性测试进行了两次,结果相似。据我们所知,这是意大利关于立枯丝核菌侵染长春花的首次报道。印度(1)和美国(3)也报道过相同病害。参考文献:(1)R. Balasubramanian和K. S. Bhama。《印度植物病理学》30:556,1977年。(2)D. E. Carling。通过菌丝融合反应对立枯丝核菌进行分组。载于:《立枯丝核菌属:分类学、分子生物学、生态学、病理学及病害防治》。B. Sneh等人编著。荷兰Kluwer学术出版社,1996年,第37 - 47页。(3)A. K. Hagan和J. M. Mullen。《植物病害》77:1169,1993年。(4)B. Sneh等人。《立枯丝核菌属的鉴定》。美国植物病理学会,明尼苏达州圣保罗,1991年。