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疫霉引起的瑞香颈基腐病和根腐病在意大利的首次报道

First Report of Collar and Root Rot Caused by Phytophthora nicotianae on Daphne odora in Italy.

作者信息

Garibaldi A, Bertetti D, Gullino M L

机构信息

Centre of Competence for the Innovation in the Agro-Environmental Sector (AGROINNOVA), Via Leonardo da Vinci 44, 10095 Grugliasco, Italy.

出版信息

Plant Dis. 2009 Aug;93(8):848. doi: 10.1094/PDIS-93-8-0848A.

DOI:10.1094/PDIS-93-8-0848A
PMID:30764353
Abstract

Daphne odora is becoming popular in gardens because of its variegated foliage and fragrant flowers in late winter and early spring. During October of 2008 in a commercial nursery near Maggiore Lake (Verbano-Cusio-Ossola Province) in northwestern Italy, plants of D. odora showed extensive chlorosis and root rot. Diseased plants eventually wilted and died, dropping leaves in some cases. Most frequently, wilted leaves persisted on stems. At the soil level, dark brown-to-black water-soaked lesions that coalesced often girdled the stem. All of the crown and root system was affected. Disease was widespread and severe with 70% of 2,500 potted plants being affected. A Phytophthora-like organism was isolated consistently on a medium selective for oomycetes (4) after disinfestation of lower stem and root pieces of D. odora for 1 min in a solution containing 1% NaOCl. Tissue fragments of 1 mm were excised from the margins of the lesions and plated. The pathogen was identified based on morphological and physiological features as Phytophthora nicotianae (= P. parasitica) (2). Sporangia were produced for identification by growing a pure culture in sterilized soil extract solution at neutral pH (obtained by shaking and then centrifuging 300 g of soil in 1 liter of distilled water). They were spherical to ovoid, papillate, and measured 39.2 to 54.5 × 31.7 to 41.7 μm (average 44.8 × 34.5 μm). Papillae measured 2.4 to 4.9 μm (average 3.7 μm). Chlamydospores were spherical with a diameter ranging from 15.8 to 36.1 μm (average 25.4 μm). The internal transcribed spacer (ITS) region of rDNA of a single isolate was amplified using primers ITS4/ITS6 and sequenced. BLAST analysis (1) of the 804-bp segment showed a 100% homology with the sequence of P. nicotianae EF140988. The nucleotide sequence has been assigned GenBank No. FJ843100. Pathogenicity of two isolates obtained from infected plants was confirmed by inoculating 12-month-old plants of D. odora. Both isolates were grown for 15 days on a mixture of 70:30 wheat/hemp kernels and then 80 g/liter of the inoculum was mixed into a substrate containing sphagnum peat moss/pumice/pine bark/clay (50:20:20:10 vol/vol). One plant per 3-liter pot was transplanted into the substrate and constituted the experimental unit. Three replicates were used for each isolate and noninoculated control treatment; the trial was repeated once. All plants were kept in a greenhouse at temperatures from 20 to 25°C. Plants inoculated with isolate no. 1 developed symptoms of chlorosis and root rot within 14 days and then a wilt rapidly followed. Isolate no. 2 was less aggressive causing the same symptoms within 20 days. Control plants remained symptomless. P. nicotianae consistently was reisolated from inoculated plants. Previously, P. nicotianae (= P. parasitica) has been reported in several states of the United States on D. odora (3). To our knowledge, this is the first report of P. nicotianae on D. odora in Italy. The economic importance of the disease is low because of the limited number of farms that grow this crop in Italy, although spread could increase as the popularity of plantings expand. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997 (2) D. C. Erwin and O. K. Ribeiro. Phytophthora Diseases Worldwide. The American Phytopathological Society, St Paul, MN, 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) H. Masago et al. Phytopathology, 67:425, 1977.

摘要

瑞香因其叶色斑驳以及在冬末和早春绽放的芬芳花朵而在园林中越来越受欢迎。2008年10月,在意大利西北部靠近马焦雷湖(韦尔巴诺-库西奥-奥索拉省)的一家商业苗圃中,瑞香植株出现了大面积黄化和根腐现象。患病植株最终枯萎死亡,有些情况下还会落叶。最常见的情况是,枯萎的叶子仍附着在茎上。在土壤层面,深褐色至黑色的水渍状病斑常常融合在一起,环绕着茎部。整个植株的冠部和根系都受到了影响。病害传播广泛且严重,2500盆盆栽植物中有70%受到了感染。在将瑞香叶下茎段和根段在含1%次氯酸钠的溶液中消毒1分钟后,在一种对卵菌有选择性的培养基上(4)持续分离出一种类似疫霉的生物体。从病斑边缘切下1毫米的组织碎片进行平板接种。根据形态和生理特征,该病原体被鉴定为烟草疫霉(=寄生疫霉)(2)。通过在中性pH值的无菌土壤提取液中培养纯培养物来产生孢子囊用于鉴定(通过将300克土壤在1升蒸馏水中振荡然后以300克离心获得)。它们呈球形至卵形,具乳突,大小为39.2至54.5×31.7至41.7微米(平均44.8×34.5微米)。乳突大小为2.4至4.9微米(平均3.7微米)。厚垣孢子呈球形,直径范围为15.8至36.1微米(平均25.4微米)。使用引物ITS4/ITS6扩增单个分离物的rDNA内部转录间隔区(ITS)并进行测序。对804碱基对片段的BLAST分析(1)显示与烟草疫霉EF140988的序列有100%的同源性。该核苷酸序列已被赋予GenBank登录号FJ843100。通过接种12个月大的瑞香植株,证实了从受感染植株中获得的两个分离物的致病性。将两个分离物在70:30的小麦/麻籽混合物上培养15天,然后将80克/升的接种物混入含有泥炭藓/浮石/松树皮/粘土(50:20:20:10体积/体积)的基质中。每3升花盆中移植一株植物,构成实验单元。每个分离物和未接种对照处理使用三个重复;试验重复一次。所有植物都保存在温度为20至25°C的温室中。接种分离物1的植物在14天内出现黄化和根腐症状,随后迅速枯萎。分离物2的致病性较弱,在20天内出现相同症状。对照植物无症状。从接种植物中持续重新分离出烟草疫霉。此前,在美国的几个州已报道烟草疫霉(=寄生疫霉)感染瑞香(3)。据我们所知,这是意大利首次报道烟草疫霉感染瑞香。由于在意大利种植这种作物的农场数量有限,该病的经济重要性较低,尽管随着种植面积的扩大,病害传播可能会增加。参考文献:(1)S. F. Altschul等人,《核酸研究》25:3389,1997年 (2)D. C. Erwin和O. K. Ribeiro,《全球疫霉病害》,美国植物病理学会,明尼苏达州圣保罗,1996年 (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,明尼苏达州圣保罗,1989年 (4)H. Masago等人,《植物病理学》,67:425,1977年

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