Garibaldi A, Gilardi G, Bertetti D, Gullino M L
Center of Competence AGROINNOVA, University of Torino, Via Leonardo da Vinci, 44, 10095 Grugliasco, Italy.
Plant Dis. 2009 Apr;93(4):433. doi: 10.1094/PDIS-93-4-0433A.
Aquilegia flabellata (Ranunculaceae), fan columbine, is a perennial herbaceous plant with brilliant blue-purple flowers with white petal tips. It can also be grown for cut flower production. In April of 2008, in several nurseries located near Biella (northern Italy), a leaf blight was observed on 10 to 15% of potted 30-day-old plants grown on a sphagnum peat substrate at 15 to 20°C and relative humidity of 80 to 90%. 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 over several days along the midvein until the entire leaf was destroyed. Blighted leaves turned brown, withered, and abscised. Severely infected plants died. Diseased tissue was disinfested for 10 s in 1% NaOCl, rinsed with sterile water, and plated on potato dextrose agar (PDA) amended with 25 mg/liter streptomycin sulfate. A fungus with the morphological characteristics of Rhizoctonia solani was consistently recovered, then transferred and maintained in pure culture. Ten-day-old mycelium grown on PDA at 22 ± 1°C appeared light brown, rather compact, and had radial growth. Sclerotia were not present. Isolates obtained from affected plants successfully anastomosed with tester isolate AG 4 (AG 4 RT 31, obtained from tobacco plants). Results were consistent with other reports on anastomosis reactions (2). Pairings were also made with tester isolates of AG 1, 2.1, 2.2, 3, 6, 7, 11, and BI with no anastomoses observed between the recovered and tester isolates. The internal transcribed spacer (ITS) region of rDNA was amplified using primers ITS4/ITS6 and sequenced. BLASTn analysis (1) of the 648-bp fragment showed a 100% homology with the sequence of R. solani AG-4 AB000018. The nucleotide sequence has been assigned GenBank Accession No. FJ 534555. For pathogenicity tests, the inoculum of R. solani was prepared by growing the pathogen on PDA for 10 days. Five plants of 30-day-old A. flabellata were grown in 3-liter pots. Inoculum consisting of an aqueous suspension of PDA and mycelium disks (5 g of mycelium + agar per plant) was placed at the collar of plants. Five plants inoculated with water and PDA fragments alone served as control treatments. Plants were maintained in a greenhouse at temperatures between 20 and 24°C. The first symptoms, similar to those observed in the nursery, developed 7 days after the artificial inoculation. R. solani was consistently reisolated from infected leaves and stems. Control plants remained healthy. The pathogenicity test was carried out twice with similar results. The presence of R. solani AG1-IB on A. flabellata has been reported in Japan (4), while in the United States, Rhizoctonia sp. is described on Aquilegia sp. (3). This is, to our knowledge, the first report of leaf blight of A. flabellata caused by R. solani in Italy as well as in Europe. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) D. E. Carling. Grouping in Rhizoctonia solani by hyphal anastomosis reactions. In: Rhizoctonia Species: Taxonomy, Molecular Biology, Ecology, Pathology and Disease Control. Kluwer Academic Publishers, The Netherlands, 1996. (3) D. F. Farr et al. Fungi on Plants and Products in the United States. The American Phytopathological Society, St Paul, MN, 1989. (4) E. Imaizumi et al. J. Gen. Plant Pathol. 66:210, 2000.
扇叶耧斗菜(毛茛科),是一种多年生草本植物,开着亮蓝紫色花朵,花瓣尖端为白色。它也可用于切花生产。2008年4月,在位于比耶拉(意大利北部)附近的几家苗圃中,人们观察到在以水苔泥炭为基质、温度为15至20°C、相对湿度为80至90%的条件下培育30天的盆栽植株中,有10%至15%出现了叶枯病。在叶片与叶柄交界处的土壤线以上部位以及随后沿着叶缘出现了半圆形的水渍状病斑。病斑在几天内沿着叶脉扩展,直至整片叶子坏死。枯萎的叶子变为褐色、干枯并脱落。严重感染的植株死亡。将患病组织在1%的次氯酸钠中消毒10秒,用无菌水冲洗后,接种到添加了25毫克/升硫酸链霉素的马铃薯葡萄糖琼脂(PDA)培养基上。始终能分离出具有立枯丝核菌形态特征的真菌,然后将其转移至纯培养物中并保存。在22±1°C条件下在PDA培养基上生长10天的菌丝体呈浅褐色,相当致密,有径向生长。未形成菌核。从患病植株上分离得到的菌株与测试菌株AG 4(从烟草植株上获得AG 4 RT 31)成功融合。结果与其他关于融合反应的报道一致(2)。还与AG 1、2.1、2.2,、3、6、7、11和BI的测试菌株进行了配对,在分离得到的菌株与测试菌株之间未观察到融合现象。使用引物ITS4/ITS6扩增rDNA的内部转录间隔区(ITS)并进行测序。对648碱基对片段的BLASTn分析(1)显示与立枯丝核菌AG-4 AB000018的序列具有100%的同源性。该核苷酸序列已被赋予GenBank登录号FJ 534555。为进行致病性测试,通过在PDA培养基上培养病原菌10天来制备立枯丝核菌接种物。将5株30天大的扇叶耧斗菜种植在3升花盆中。由PDA和菌丝体圆盘(每株植物5克菌丝体+琼脂)的水悬浮液组成的接种物放置在植株的颈部。5株仅接种水和PDA片段的植株作为对照处理。将植株置于温度为20至24°C的温室中。人工接种7天后出现了与在苗圃中观察到的相似的最初症状。始终能从受感染的叶片和茎中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。在日本曾报道过扇叶耧斗菜上存在立枯丝核菌AG1-IB(4),而在美国,在耧斗菜属植物上描述过丝核菌属(3)。据我们所知,这是意大利以及欧洲首次关于由立枯丝核菌引起的扇叶耧斗菜叶枯病的报道。参考文献:(1)S. F. Altschul等人。核酸研究。25:3389,1997。(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、病理学和病害防治。荷兰Kluwer学术出版社,1996。(3)D. F. Farr等人。美国植物和产品上的真菌。美国植物病理学会,圣保罗,明尼苏达州,1989。(4)E. Imaizumi等人。植物病理学报。66:210,2000。