Koike S T
University of California Cooperative Extension, Salinas 93901.
Plant Dis. 2008 Aug;92(8):1253. doi: 10.1094/PDIS-92-8-1253B.
In 2006 and 2007, severely diseased strawberry (Fragaria × ananassa) plants were observed in five commercial fields in southern California (Orange County). Disease generally occurred in discrete patches. Within such patches, disease incidence ranged from 10 to 75%. Symptoms consisted of wilting of foliage, drying and death of older leaves, plant stunting, and eventual collapse and death of plants. When plant crowns were dissected, internal vascular and cortex tissues were dark brown to orange brown. Fruiting bodies or other fungal structures were not observed. A fungus was consistently isolated from symptomatic crown tissue that had been surface sterilized and placed on acidified corn meal agar (LA-CMA). All isolates produced numerous, dark, irregularly shaped sclerotia that were 67 to 170 μm long and 44 to 133 μm wide. When isolates were grown on 1.5% water agar with dried and sterilized wheat straw, dark, ostiolate pycnidia and hyaline, single-celled, cylindrical conidia were produced. On the basis of these characters, all isolates were identified as Macrophomina phaseolina (1). The symptomatic plants tested negative for Colletotrichum spp., Phytophthora spp., Verticillium dahliae, and other pathogens. Inoculum for pathogenicity tests was produced by growing six isolates on CMA on which sterilized wood toothpicks were placed on the agar surface. After 1 week, toothpicks were removed and inserted 4 to 5 mm deep into the basal crown tissue of potted strawberry plants (cv. Camarosa) grown in soilless, peatmoss-based rooting medium. Ten plants were inoculated per isolate and one toothpick was inserted per plant. Ten control strawberry plants were treated by inserting one sterile toothpick into each crown. All plants were then grown in a shadehouse. After 2 weeks, all inoculated plants began to show wilting and decline of foliage. By 4 weeks, all inoculated plants had collapsed. Internal crown tissue was discolored and similar in appearance to the original field plants. M. phaseolina was isolated from all inoculated plants. Control plants did not exhibit any disease symptoms, and crown tissue was symptomless. The test was repeated and the results were similar. While M. phaseolina has been periodically associated with strawberry in California (3), to my knowledge, this is the first report of charcoal rot disease on commercial strawberry in California. Charcoal rot of strawberry has been reported in Egypt, France, India, Israel, and the United States (Florida and Illinois) (2,4). Similar to previous reports (2,4), many of the affected California fields were not preplant fumigated with methyl bromide + chloropicrin fumigants, and it is possible that under these changing production practices this pathogen may increase in importance in California. References: (1) P. Holliday and E. Punithalingam. No. 275 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, Surrey, UK, 1970. (2) J. Mertely et al. Plant Dis.89:434, 2005. (3) S. Wilhelm. Plant Dis. Rep. 41:941, 1957. (4) A. Zveibil and S. Freeman. Plant Dis. 89:1014, 2005.
2006年和2007年,在南加利福尼亚州(奥兰治县)的5个商业种植园中观察到了病情严重的草莓(凤梨草莓)植株。病害通常呈离散斑块状发生。在这些斑块内,发病率为10%至75%。症状包括叶片萎蔫、老叶干枯死亡、植株矮化,最终植株倒伏死亡。解剖植株冠部时,内部维管束和皮层组织呈深褐色至橙褐色。未观察到子实体或其他真菌结构。从经表面消毒并置于酸化玉米粉琼脂(LA-CMA)上的有症状冠部组织中始终能分离出一种真菌。所有分离物均产生大量深色、形状不规则的菌核,菌核长67至170μm,宽44至133μm。当分离物在含有干燥灭菌麦秸的1.5%水琼脂上生长时,会产生深色、有孔口的分生孢子器和透明、单细胞、圆柱形的分生孢子。基于这些特征,所有分离物均被鉴定为菜豆壳球孢(1)。有症状的植株对炭疽菌属、疫霉属、大丽轮枝菌和其他病原体检测呈阴性。致病性测试的接种物是通过在CMA上培养6个分离物产生的,在琼脂表面放置灭菌的木牙签。1周后,取出牙签并插入以泥炭藓为基质的无土生根培养基中生长的盆栽草莓植株(品种为卡玛罗莎)的基部冠部组织中,深度为4至5mm。每个分离物接种10株植物,每株植物插入1根牙签。10株对照草莓植株通过在每个冠部插入1根无菌牙签进行处理。然后将所有植株置于遮荫棚中生长。2周后,所有接种的植株开始出现叶片萎蔫和衰退。到4周时,所有接种的植株都已倒伏。内部冠部组织变色,外观与原始田间植株相似。从所有接种的植株中分离出了菜豆壳球孢。对照植株未表现出任何病害症状,冠部组织无症状。该试验重复进行,结果相似。虽然菜豆壳球孢在加利福尼亚州曾周期性地与草莓相关联(3),但据我所知,这是加利福尼亚州商业草莓上炭腐病的首次报道。埃及、法国、印度、以色列和美国(佛罗里达州和伊利诺伊州)均报道过草莓炭腐病(2,4)。与之前的报道(2,4)相似,许多受影响的加利福尼亚州种植园在种植前未用甲基溴+氯化苦熏蒸剂进行熏蒸,在这些不断变化的生产方式下,这种病原体在加利福尼亚州的重要性可能会增加。参考文献:(1)P. Holliday和E. Punithalingam。载于《病原真菌和细菌描述》第275号。英国皇家植物园真菌研究所,英国萨里郡邱园,1970年。(2)J. Mertely等人。《植物病害》89:434,2005年。(3)S. Wilhelm。《植物病害报告》41:941,1957年。(4)A. Zveibil和S. Freeman。《植物病害》89:1014,2005年。