Gumtow R L, Khan A A, Bocsanczy A M, Yuen J M F, Palmateer A J, Norman D J
Department of Plant Pathology, University of Florida-IFAS, Mid-Florida Research and Education Center, 2725 Binion Rd., Apopka, FL 32703.
Tropical Research and Education Center, Homestead, FL 33031.
Plant Dis. 2013 Jun;97(6):836. doi: 10.1094/PDIS-12-12-1117-PDN.
Duranta erecta (Verbenaceae) is used extensively in southern states as an ornamental shrub and has replaced boxwood as the most common short hedge accenting flower beds. Over the past 2 years, during warm wet periods, dark necrotic leaf spots have been observed on golden dewdrop plants in Florida. Isolations from these spots on Difco nutrient agar (NA) consistently yielded two types of bacterial colonies that were not always simultaneously present: 1) round butyrous, bright yellow and 2) flat cream-colored. Both were 2 mm in size after 48 h, gram-negative, and produced a hypersensitivity reaction (HR) on tobacco cv Hicks. Yellow colony bacteria were oxidase negative and non-fluorescent on King's medium B (KMB) (1). Cream-colored colony bacteria were oxidase positive and fluorescent on KMB. Three isolates of both types were selected for further study. Partial 16S rDNA sequencing and fatty acid analysis (FAME) MIDI Microbial Identification System (Microbial ID, Inc., Newark, DE) were used for identification of strains. The 16S rDNA primers used were; forward primer AMB14 5'-TCCAGCAATGCCGCGTGTGT-3' and reverse primer AMB13 5'-CATCCACCGCTTGTGCGGGT-3'. The PCR program consisted of an initial denaturing cycle of 95°C for 2 min followed by 30 cycles of denaturing at 95°C for 30 s, annealing at 60°C for 40 s and extension at 72°C for 1 min and one final extension at 72°C for 10 min. Using FAME analysis, the three strains of the cream-colored colony type were identified as Pseudomonas cichorii with high similarity values (0.907, 0.961, 0.819) and this corresponded well with the 16S rDNA sequences where 99% sequence identity was observed with P. cichorii strain JBC1 16S ribosomal RNA gene, partial sequence GenBank Accession No. JF951725. Two of the three yellow colony strains were identified by MIDI FAME profiles as Xanthomonas axonopodis pv. manihotis with similarity coefficients of 0.767 and 0.826. The third strain had a low similarity match to X. a. pv. carotae (0.541). The 16S rDNA sequencing of these strains showed 98% sequence identity to X. citri subsp. citri strain SA1 16S ribosomal RNA gene only, partial sequence identity JQ890091.1, thus indicating a possible undescribed X. axonopodis pathovar. To satisfy Koch's postulates, three golden dewdrop 'Golden Mound' plants were sprayed with a suspension of 10 CFU/ml of a 2-day NA culture of each strain, bagged for 24 h to raise humidity, and placed in a greenhouse. A strain of P. cichorii (P409) isolated from chrysanthemum was used as a positive control when comparing cream-colored strains. A saline buffered control was used as a negative control. Within 3 weeks, leaf spots developed on plants sprayed with each of the six strains, including positive control strain of P. cichorii. Reisolations yielded the same type of colony as the originally inoculated strain. Inoculation experiments were repeated three times with a minimum of three plants per isolate with similar results. To our knowledge, this is the first report in the United States of bacterial leaf spot caused by P. cichorii and X. axonopodis on golden dewdrop. An earlier morphological and physiological description of a Xanthomonas sp. was done on Duranta in India in 1962 (2). Due to the difficulty in controlling bacterial diseases and the popularity of Duranta spp. in the landscape, these diseases may present a problem in ornamental trade. References: (1) E. O. King et al. J. Lab. Clin. Med. 44:301, 1954. (2) M. C. Srinivasan et al. Proc. Indian Acad. Sci. 56:88, 1962.
金露花(马鞭草科)在南部各州被广泛用作观赏灌木,已取代黄杨木成为装点花坛最常见的矮篱。在过去两年中,在温暖潮湿的时期,佛罗里达州的金露花植株上出现了深色坏死叶斑。在迪夫科营养琼脂(NA)上从这些斑点进行分离,始终产生两种并非总是同时出现的细菌菌落:1)圆形、奶油状、亮黄色;2)扁平、米色。48小时后两者大小均为2毫米,革兰氏阴性,并且在烟草品种希克斯上产生过敏反应(HR)。黄色菌落细菌氧化酶阴性,在金氏培养基B(KMB)上无荧光(1)。米色菌落细菌氧化酶阳性,在KMB上有荧光。每种类型选择三个分离株进行进一步研究。使用部分16S rDNA测序和脂肪酸分析(FAME)MIDI微生物鉴定系统(微生物鉴定公司,纽瓦克,特拉华州)对菌株进行鉴定。使用的16S rDNA引物为:正向引物AMB14 5'-TCCAGCAATGCCGCGTGTGT-3'和反向引物AMB13 5'-CATCCACCGCTTGTGCGGGT-3'。PCR程序包括95°C初始变性循环2分钟,随后95°C变性30秒、60°C退火40秒、72°C延伸1分钟共30个循环,最后72°C延伸10分钟。通过FAME分析,三种米色菌落类型的菌株被鉴定为菊苣假单胞菌,相似度值较高(0.907、0.961、0.819),这与16S rDNA序列很好地对应,其中观察到与菊苣假单胞菌菌株JBC1的16S核糖体RNA基因有99%的序列同一性,部分序列GenBank登录号为JF951725。三个黄色菌落菌株中的两个通过MIDI FAME图谱鉴定为野油菜黄单胞菌菜豆致病变种,相似度系数分别为0.767和0.826。第三个菌株与胡萝卜软腐欧文氏菌有低相似度匹配(0.541)。这些菌株的16S rDNA测序显示仅与柑桔黄单胞菌柑桔亚种菌株SA1的16S核糖体RNA基因有98%的序列同一性,部分序列同一性为JQ890091.1,因此表明可能是一种未描述的野油菜黄单胞菌致病变种。为满足科赫法则,用每种菌株2天的NA培养物制成的10CFU/ml悬浮液喷洒三株金露花“金色山丘”植株,套袋24小时以提高湿度,然后置于温室中。在比较米色菌株时,使用从菊花中分离的一株菊苣假单胞菌(P409)作为阳性对照。使用盐缓冲液对照作为阴性对照。在3周内,用六种菌株中的每一种喷洒的植株上都出现了叶斑,包括菊苣假单胞菌阳性对照菌株。再次分离得到与最初接种菌株相同类型的菌落。接种实验重复三次,每个分离株至少用三株植物,结果相似。据我们所知,这是美国首次关于菊苣假单胞菌和野油菜黄单胞菌引起金露花叶斑病的报道。1962年在印度对金露花上的一种黄单胞菌进行了早期的形态学和生理学描述(2)。由于控制细菌病害困难且金露花属植物在园林中很受欢迎,这些病害可能在观赏植物贸易中造成问题。参考文献:(1)E.O.金等人,《临床检验杂志》44:301,1954年。(2)M.C.斯里尼瓦桑等人,《印度科学院学报》56:88,1962年。