Koike S T, Kirkpatrick S C, Gordon T R
University of California Cooperative Extension, Salinas 93901.
Department of Plant Pathology, University of California, Davis 95616.
Plant Dis. 2009 Oct;93(10):1077. doi: 10.1094/PDIS-93-10-1077A.
Beginning in 2006 and continuing into 2009, an apparently new disease of strawberry (Fragaria × ananassa) affected commercial plantings (cvs. Albion, Camarosa, and others) in coastal (Ventura and Santa Barbara counties) California. Symptoms consisted of wilting of foliage, drying and withering of older leaves, stunting of plants, and reduced fruit production. Plants eventually collapsed and died. Internal vascular and cortical tissues of plant crowns showed a brown-to-orange-brown discoloration. Differences in cultivar susceptibility were not recorded. Internal crown and petiole tissues, when placed on acidified corn meal agar, consistently yielded Fusarium isolates having similar colony morphologies. No other pathogens were isolated. The Fusarium isolates were subcultured on carnation leaf agar and observed to be producing macroconidia and microconidiophores that are diagnostic of Fusarium oxysporum (1). For two of these isolates, the internal transcribed spacer region comprising ITS1, ITS2, and 5.8S rRNA was amplified using primers ITS-1 and ITS-4 (3). On the basis of a comparison of 515 bp, both isolates had the identical sequence, which was a 100% match for 30 accessions of F. oxysporum in GenBank. This comparison included several formae speciales of F. oxysporum, but F. oxysporum f. sp. fragariae, a previously described pathogen of strawberry (4), was not included. The isolates are archived in the Department of Plant Pathology at UC Davis and are available on request. Both sequenced isolates plus four others were tested for pathogenicity on strawberries. For these tests, spore suspensions of 1 × 10 conidia/ml were prepared separately for six isolates. Roots of strawberry transplants (12 plants of cv. Camino Real) were cut and soaked in spore suspensions for 10 min. Plants were potted in soilless, peat moss-based medium in containers. Control strawberry plants were soaked in water prior to planting. All plants were then grown in a shadehouse. After 8 weeks, inoculated plants began to show wilting and decline of foliage and internal crown tissue was lightly discolored. F. oxysporum was isolated from all inoculated plants. Control plants did not exhibit any disease symptoms and crown tissue was symptomless. To our knowledge, this is the first report of Fusarium wilt of strawberry in California. This disease has been reported from a number of other countries including Argentina, Australia, China, South Korea, Spain, and Japan (2). Since 2006, Fusarium wilt of strawberry has increased in incidence and severity in California. Initial problems in 2006 consisted of multiple small patches (2 to 4 beds wide × 3 to 10 m long) of diseased plants; in these patches disease incidence could range from 80 to 100%. By 2009, in some fields, the disease affected large sections that ran the length of the field. References: (1) P. E. Nelson et al. Fusarium Species: An Illustrated Manual for Identification. Pennsylvania State University Press, University Park, 1983. (2) H. S. Okamoto et al. Plant Prot. 24:231, 1970. (3) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Application. Academic Press, NY, 1993. (4) B. L. Winks and Y. N. Williams. Qld. J. Agric. Anim. Sci. 22:475, 1966.
从2006年开始一直持续到2009年,一种明显新型的草莓(凤梨草莓)病害影响了加利福尼亚沿海地区(文图拉县和圣巴巴拉县)的商业种植园(品种包括阿尔比恩、卡马罗萨等)。症状包括叶片萎蔫、老叶干枯和凋零、植株矮化以及果实产量降低。植株最终枯萎死亡。植株冠部的内部维管束和皮层组织呈现出褐色至橙褐色变色现象。未记录到品种易感性的差异。将内部冠部和叶柄组织放置在酸化玉米粉琼脂上时,始终能分离出具有相似菌落形态特征的镰刀菌。未分离出其他病原体。将镰刀菌分离株转接至香石竹叶琼脂上继代培养,观察到其产生了可诊断尖孢镰刀菌的大型分生孢子和小型分生孢子梗(1)。对于其中两个分离株,使用引物ITS - 1和ITS - 4扩增包含ITS1、ITS2和5.8S rRNA的内部转录间隔区(3)。基于515 bp的比对,两个分离株具有相同序列,与GenBank中30个尖孢镰刀菌登录号的序列100%匹配。该比对包括尖孢镰刀菌的几个专化型,但未包括先前描述的草莓病原菌尖孢镰刀菌草莓专化型(4)。这些分离株保存在加利福尼亚大学戴维斯分校植物病理学系,可应要求提供。对两个测序分离株以及另外四个分离株进行了对草莓的致病性测试。对于这些测试,分别为六个分离株制备了浓度为1×10⁶ 个分生孢子/ml的孢子悬浮液。将草莓移栽苗(卡米诺雷亚尔品种的12株植株)的根系切断并在孢子悬浮液中浸泡10分钟。将植株种植在无土、以泥炭藓为基质的培养基容器中。对照草莓植株在种植前浸泡在水中。然后所有植株在遮荫棚中生长。8周后,接种植株开始出现萎蔫和叶片衰退现象,内部冠部组织轻微变色。从所有接种植株中分离出尖孢镰刀菌。对照植株未表现出任何病害症状,冠部组织无症状。据我们所知,这是加利福尼亚草莓枯萎病的首次报道。包括阿根廷、澳大利亚、中国、韩国、西班牙和日本在内的许多其他国家也报道过这种病害(2)。自2006年以来,加利福尼亚草莓枯萎病的发病率和严重程度有所增加。2006年最初的问题是出现多个患病植株的小斑块(宽2至4畦×长3至10米);在这些斑块中,病害发病率可达80%至100%。到2009年,在一些田地中,该病影响了整块田地的大片区域。参考文献:(1)P. E. Nelson等人,《镰刀菌物种:鉴定图谱手册》,宾夕法尼亚州立大学出版社,大学园,1983年。(2)H. S. Okamoto等人,《植物保护》24:231,1970年。(3)T. J. White等人,载于《PCR协议:方法与应用指南》第315页,学术出版社,纽约,1993年。(4)B. L. Winks和Y. N. Williams,《昆士兰农业与动物科学杂志》22:475,1966年。