Friskop A, Kinzer K, McConnell M, Liu Z, Korus K, Timmerman A, Jackson T
Department of Plant Pathology, North Dakota State University, Fargo, ND 58108-6050.
Department of Plant Pathology, University of Nebraska-Lincoln 68583-0722.
Plant Dis. 2014 Dec;98(12):1739. doi: 10.1094/PDIS-04-14-0397-PDN.
In August of 2011, the North Dakota State University Plant Diagnostic Lab received a hybrid corn (Zea mays) leaf sample from Burleigh County in south-central North Dakota (ND). The leaf had long, irregular, water-soaked lesions consistent with Goss's leaf blight of corn. Using a light microscope at 10× magnification, bacterial streaming was observed from the excised edge of leaf tissue. A bacterial suspension was created, streaked onto a semi-selective CNS medium (1), and incubated at 22°C. Dark yellow-orange colonies appeared on the medium after 5 days. Single colonies were subcultured onto additional CNS media. To verify the identity of the bacterial isolate, PCR amplification of the 16S ribosomal DNA from this isolate along with a known Clavibacter michiganensis spp. nebraskensis (Cmn) isolate collected in Indiana (4) was performed using the eubacterial universal primers 27f and 1525r (3). The 1,431-bp 16S rDNA region was obtained for each isolate and they were compared with each other and with those deposited in NCBI GenBank. Sequence alignment identified only one nucleotide difference between the ND isolate and the Indiana isolate. BLASTn search against the NCBI database showed the first 100 hits were described as C. michiganensis or unidentified Clavibacter sp. The ND isolate had a two-nucleotide difference with Cmn isolate NCPPB2581 (HE614873), and a three nucleotide difference was found with the C. michiganensis spp. michiganensis isolate NCPPB 382 (AM711867). To satisfy Koch's postulates, eight corn plants (Golden Cross Bantam) were grown in the greenhouse at 22 to 24°C. Four corn plants were inoculated at growth stage V4-V5 using a suspension of approximately 1 × 10 CFU/ml from cultures grown on CNS for 6 days. Wounds were created on the fifth leaf approximately 7 cm from the leaf tip using a tongue-seizing forceps outfitted with a rubber stopper composed of pins (2). Simultaneously, 1 ml of the bacterial suspension was delivered into the wounds through a hole on top of the rubber stopper. Four control plants were inoculated with sterile water in a similar fashion. No symptoms were observed on the control plants. After 6 days, long water-soaked symptoms were observed on leaves inoculated with the bacterial suspension. Using leaves with water-soaked lesions, the pathogen was re-isolated onto CNS media and subjected to PCR amplification, and the resulting amplicons were sequenced as before. The sequence of the amplicon from the re-isolation matched that of the original ND isolate. To our knowledge, this is the first account of Goss's leaf blight and wilt identified in ND. As the corn acreage and no-till production systems in the state have increased, the economic implications of this disease may become more significant. Recognition of symptoms and proper identification of this bacterial disease in the field should help reduce unnecessary foliar fungicide sprays. References: (1) D. C. Gross and A. K. Vidaver. Phytopathology 69:82, 1979. (2) W. A. Hagborg. Can. J. Bot. 48:1135, 1970. (3) X. Li and S. H. DeBoer. Can. J. Microbiol. 41:925, 1995. (4) G. Ruhl et al. Plant Dis. 93:841, 2009.
2011年8月,北达科他州立大学植物诊断实验室收到一份来自北达科他州中南部伯利县的杂交玉米(玉米)叶片样本。叶片上有长而不规则的水渍状病斑,与玉米戈斯叶斑病症状相符。在10倍放大倍数的光学显微镜下,观察到从叶片组织切除边缘有细菌溢菌现象。制备细菌悬液,划线接种于半选择性CNS培养基(1)上,并在22°C下培养。5天后,培养基上出现深黄色橙色菌落。将单个菌落转接至其他CNS培养基上。为了验证细菌分离株的身份,使用真细菌通用引物27f和1525r(3)对该分离株以及从印第安纳州采集的已知内布拉斯加密歇根棒杆菌(Cmn)分离株(4)的16S核糖体DNA进行PCR扩增。每个分离株均获得了1431bp的16S rDNA区域,并将它们相互比较以及与NCBI GenBank中保存的序列进行比较。序列比对发现北达科他州分离株与印第安纳州分离株之间仅存在一个核苷酸差异。在NCBI数据库中进行BLASTn搜索显示,前100个匹配结果被描述为密歇根棒杆菌或未鉴定的棒杆菌属。北达科他州分离株与Cmn分离株NCPPB2581(HE614873)有两个核苷酸差异,与密歇根棒杆菌密歇根亚种分离株NCPPB 382(AM711867)有三个核苷酸差异。为了满足科赫法则,在22至24°C的温室中种植了8株玉米(金十字矮脚鸡)。在V4 - V5生长阶段,使用在CNS培养基上培养6天的菌悬液(约1×10 CFU/ml)对4株玉米进行接种。使用配备由大头针组成的橡胶塞的舌钳在距叶尖约7厘米的第五片叶子上造成伤口(2)。同时,通过橡胶塞顶部的孔将1ml细菌悬液注入伤口。以类似方式用无菌水接种4株对照植物。对照植物未观察到症状。6天后,在接种细菌悬液的叶片上观察到长的水渍状症状。使用有水渍状病斑的叶片,将病原菌重新分离到CNS培养基上并进行PCR扩增,所得扩增子如前所述进行测序。重新分离的扩增子序列与原始北达科他州分离株的序列匹配。据我们所知,这是北达科他州首次发现玉米戈斯叶斑病和枯萎病。随着该州玉米种植面积和免耕生产系统的增加,这种病害的经济影响可能会变得更加显著。在田间识别症状并正确鉴定这种细菌性病害应有助于减少不必要的叶面杀菌剂喷洒。参考文献:(1)D. C. Gross和A. K. Vidaver。植物病理学69:82,1979。(2)W. A. Hagborg。加拿大植物学杂志48:1135,1970。(3)X. Li和S. H. DeBoer。加拿大微生物学杂志41:925,1995。(4)G. Ruhl等人。植物病害93:841,2009。