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韩国酸腐果胶杆菌引起西瓜细菌性黑斑病的首次报道

First Report of Bacterial Black Spot Disease in Watermelon Caused by Acidovorax valerianellae in Korea.

作者信息

Han Y-K, Han K-S, Lee S-C, Kim S, Lee J

机构信息

Horticultural and Herbal Crop Environment Division, National Institute of Horticultural and Herbal Science, Rural Development Administration, Suwon 441-744, Republic of Korea.

Department of Applied Biology, Dong-A University, Busan 604-714, Republic of Korea.

出版信息

Plant Dis. 2012 May;96(5):759. doi: 10.1094/PDIS-10-11-0826.

Abstract

Watermelon (Citrullus lanatus (Thunb.) Matsum. & Nakai), an important member of the Cucurbitaceae family, is cultivated on 21,000 ha that produces 850,000 t in Korea. In April 2011, we received grafted watermelon with necrotic leaf spots from a commercial watermelon grower in Andong, Korea. Black spots were observed on cotyledons of the plants in seedbeds, and approximately 9% of watermelon plants were infected with the disease. Initial symptoms on the seedling were black, greasy spots sometimes surrounded by a halo of discoloration. Younger leaves usually showed symptoms later than cotyledons. Bacteria isolated from the infected plants were gram-negative, motile, straight rods with a single flagellum and 0.84 to 0.89 μm wide and 1.54 to 1.69 μm long. They formed rough colonies with a white-cream color after 48 h of incubation on Luria-Bertani (LB) agar at 28°C. Colonies of isolates were nonfluorescent, smooth, and white on King's medium B. On YBGA (7 g of yeast extract, 7 g of bactopeptone, 7 g of glucose, 15 g of agar, 1,000 ml of distilled water; pH 7.2) colonies are circular, raised with an entire margin, and white to cream. Pathogenicity tests were conducted with potted, greenhouse-grown watermelon plants. Bacterial colonies grown on LB medium for 48 h at 28°C were suspended in sterile distilled water, and the suspension (1.0 × 10 CFU/ml) was infiltrated into mesophyll of watermelon leaves with a syringe as previously described (2). Inoculated plants were maintained at 28°C and 90% relative humidity in a growth chamber with a daily 12-h photoperiod of fluorescent light. Five plants were used for inoculation. Sterilized distilled water was used as a control. The bacterial isolates induced necrosis in the infiltrated area within 3 to 5 days. Typical water-soaked spots appeared after 3 days of incubation and became gray to black after 6 days. The bacterium was successfully reisolated from the diseased lesions, thus completing Koch's postulates. A cell suspension (50 μl of 1 × 10 CFU/ml) was infiltrated with a syringe into the intercellular spaces of tobacco leaves to determine the hypersensitive reaction (HR). A typical HR developed 20 h after leaf infiltration. The 16S rDNA region of the isolates, amplified by using universal PCR primers, shared 99% sequence identity with an Acidovorax valerianellae strain (GenBank Accession No. AJ431731) (1). The resulting sequences of 1,424 bp were deposited in GenBank (Accession No. JN983471). The isolates we obtained in this study clustered with A. valerianellae on a phylogenetic tree generated by the neighbor-joining method implemented in MEGA Version 4.1. In the Biolog Microbial Identification System, Version 4.2 (Biolog Inc., Hayward, CA), all isolates were 63 to 77% similar with a match probability of 100% to A. konjaci. Fatty acid composition analysis of isolates based on the MIDI Library version TSBA 5.0 and Library Generation system software version 5.0 showed that the isolates were 52 and 72% similar to an Acidovorax sp., respectively. To our knowledge, this is the first report of bacterial black spot disease in watermelon caused by A. valerianellae in Korea. A. valerianellae is a causal agent of bacterial black spot in corn salad and is transmitted by inoculated seeds (3). Further studies are required to determine whether it is seed transmitted in watermelon. References: (1) L. Gardan et al. Int. J. Syst. Evol. Microbiol. 53:795, 2003. (2) C. Grondeau et al. Plant Pathol. 56:302, 2007. (3) C. Grondeau et al. Plant Pathol. 58:846, 2009.

摘要

西瓜(Citrullus lanatus (Thunb.) Matsum. & Nakai)是葫芦科的重要成员,韩国西瓜种植面积达21,000公顷,产量为850,000吨。2011年4月,我们从韩国安东的一位商业西瓜种植者那里收到了带有坏死叶斑的嫁接西瓜。在苗床中,植株的子叶上出现了黑斑,约9%的西瓜植株感染了这种病害。幼苗初期症状为黑色、油腻状斑点,有时周围有变色晕圈。较嫩的叶子通常比子叶出现症状的时间晚。从感染植株中分离出的细菌为革兰氏阴性、具运动性、直杆状,有一根单一鞭毛,宽0.84至0.89μm,长1.54至1.69μm。在28°C的Luria-Bertani(LB)琼脂上培养48小时后,它们形成粗糙的菌落,颜色为白色至淡黄色。分离菌株在King氏培养基B上的菌落无荧光、光滑且为白色。在YBGA(7克酵母提取物、7克细菌蛋白胨、7克葡萄糖、15克琼脂、1000毫升蒸馏水;pH 7.2)上,菌落呈圆形,边缘整齐凸起,颜色为白色至淡黄色。用盆栽的温室种植西瓜植株进行致病性测试。在28°C的LB培养基上培养48小时的细菌菌落悬浮于无菌蒸馏水中,按照先前描述的方法(2)用注射器将悬浮液(1.0×10 CFU/ml)注入西瓜叶片的叶肉中。接种的植株在生长室中保持在28°C和90%相对湿度,每天有12小时的荧光光照周期。使用五株植株进行接种。用灭菌蒸馏水作为对照。细菌分离物在3至5天内在注射部位诱导坏死。培养3天后出现典型的水渍状斑点,6天后变为灰色至黑色。该细菌成功地从患病病斑中重新分离出来,从而完成了柯赫氏法则。用注射器将细胞悬浮液(50μl的1×10 CFU/ml)注入烟草叶片的细胞间隙中以确定过敏反应(HR)。叶片注射20小时后出现典型的HR。使用通用PCR引物扩增的分离物的16S rDNA区域与一种细叶芹嗜酸菌菌株(GenBank登录号AJ431731)(1)的序列同一性为99%。所得的1424 bp序列已存入GenBank(登录号JN983471)。我们在本研究中获得的分离物在由MEGA 4.1版本中实施的邻接法生成的系统发育树上与细叶芹嗜酸菌聚类。在Biolog微生物鉴定系统4.2版本(Biolog公司,加利福尼亚州海沃德)中,所有分离物与魔芋嗜酸菌的相似度为63%至77%,匹配概率为100%。基于MIDI库版本TSBA 5.0和文库生成系统软件版本5.0对分离物进行的脂肪酸组成分析表明,分离物分别与一种嗜酸菌属相似52%和72%。据我们所知,这是韩国首次报道由细叶芹嗜酸菌引起的西瓜细菌性黑斑病。细叶芹嗜酸菌是玉米沙拉细菌性黑斑病的病原体,通过接种种子传播(3)。需要进一步研究以确定它是否在西瓜中通过种子传播。参考文献:(1)L. Gardan等人,《国际系统与进化微生物学杂志》53:795,2003年。(2)C. Grondeau等人,《植物病理学》56:302,2007年。(3)C. Grondeau等人,《植物病理学》58:846,2009年。

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