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丁香假单胞菌胡萝卜软腐致病变种在塞尔维亚引起胡萝卜、欧芹和防风细菌性叶斑病的首次报道

First Report of Pseudomonas syringae pv. coriandricola Causing Bacterial Leaf Spot on Carrot, Parsley, and Parsnip in Serbia.

作者信息

Popović T, Ivanović Ž, Ignjatov M, Milošević D

机构信息

Institute for Plant Protection and Environment, 11000 Belgrade, Serbia.

Institute for Field and Vegetable Crops, 21000 Novi Sad, Serbia.

出版信息

Plant Dis. 2015 Mar;99(3):416. doi: 10.1094/PDIS-10-14-1041-PDN.

Abstract

During the spring of 2014, a severe leaf spot disease was observed on carrot (Daucus carota), parsley (Petroselinum crispum), and parsnip (Pastinaca sativa) on a 0.5-ha vegetable farm in Vojvodina Province, Serbia. The disease appeared under wet and cool conditions with 5 to 25% of plants infected for each of the three crops. Symptoms were characterized as brown angular leaf spots, ~2 mm in diameter, often limited by veins. Collected symptomatic leaves were rinsed and dried at room temperature, and leaf sections taken from the margin of necrotic tissue were macerated in sterile phosphate buffer and streaked onto nutrient agar with 5% (w/v) sucrose (NAS). After isolation, whitish, circular, dome-shaped, Levan-positive colonies consistently formed. Five strains from each host (carrot, parsley, and parsnip) were used for further study. Strains were gram-negative, aerobic, and positive for catalase and tobacco hypersensitive reaction but negative for oxidase, rot of potato slices, and arginine dihydrolase. These reactions corresponded to LOPAT group Ia, which includes Pseudomonas syringae pathovars (3). Repetitive extragenic palindromic sequence (Rep)-PCR fingerprint profiles using the REP, ERIC, and BOX primers (4) were identical for all strains. Sequence typing of the housekeeping genes gyrB and rpoD (1) was performed for three representative strains (one from each host). Sequences were deposited in the NCBI GenBank database as accessions KM979434 to KM979436 (strains from carrot, parsnip, and parsley, respectively) for the gyrB gene and KM979437 to KM979439 (strains from parsnip, parsley and carrot, respectively) for the rpoD gene. Sequences were compared with pathotype strain Pseudomonas syringae pv. coriandricola ICMP12471 deposited in the Plant Associated and Environmental Microbes Database ( http://genome.ppws.vt.edu/cgi-bin/MLST/home.pl ). BLAST analysis revealed 100% homology for gyrB and 99% homology for rpoD. Pathogenicity was tested with five representative strains from each host on four-week-old plants of carrot (cv. Nantes), parsley (cv. NS Molski), and parsnip (cv. Dugi beli glatki) using two methods: spraying the bacterial suspension (10 CFU ml) on the leaves until runoff (5) and injecting the bacterial suspension into leaves with a hypodermic syringe (2). Four plants were used per strain and method. Sterile distilled water was applied as a negative control treatment for each plant species. All plants were kept in a mist room with 100% humidity for 4 h, then transferred to a greenhouse at 25°C and 80% relative humidity and examined for symptom development over a period of three weeks. For all strains, inoculated leaves first developed water-soaked lesions on the leaves 5 to 7 days after inoculation (DAI); 14 DAI lesions became dark brown, often surrounded by haloes. No symptoms were observed on control plants inoculated with sterile distilled water. For fulfillment of Koch's postulates, re-isolations were done onto NAS. Re-isolated bacteria were obtained from each inoculated host and confirmed to be identical to the original isolates using the LOPAT tests and Rep-PCR fingerprinting profiles. Based on the pathogenicity test accompanied by completion of Koch's postulates, sequence analysis, and bacteriological tests, the strains were identified as P. s. pv. coriandricola. To our knowledge, this is the first report of bacterial leaf spot of carrot, parsley, and parsnip in Serbia. It may present a threat to production due to quality requirements for fresh market. References: (1) P. Ferrente and M. Scortichini. Plant Pathol. 59:954, 2010. (2) M. Gupta et al. Plant Dis. 97:418, 2013. (3) R. A. Lelliott et al. J. Appl. Bacteriol. 29:470, 1966. (4) F. J. Louws et al. Appl. Environ. Microb. 60:2286, 1994. (5) X. Xu and S. A. Miller. Plant Dis. 97:988, 2013.

摘要

2014年春季,在塞尔维亚伏伊伏丁那省一个0.5公顷的蔬菜农场中,胡萝卜(Daucus carota)、欧芹(Petroselinum crispum)和防风草(Pastinaca sativa)上观察到一种严重的叶斑病。该病在潮湿凉爽的条件下出现,三种作物中每种都有5%至25%的植株受到感染。症状表现为褐色角状叶斑,直径约2毫米,常受叶脉限制。采集有症状的叶片,用清水冲洗后在室温下干燥,从坏死组织边缘取叶片切片在无菌磷酸盐缓冲液中研磨,然后划线接种到含5%(w/v)蔗糖的营养琼脂(NAS)上。分离后, consistently形成了白色、圆形、圆顶状、勒范氏阳性菌落。从每个寄主(胡萝卜、欧芹和防风草)中选取5个菌株用于进一步研究。这些菌株革兰氏阴性、需氧,过氧化氢酶和烟草过敏反应呈阳性,但氧化酶、马铃薯切片腐烂和精氨酸双水解酶呈阴性。这些反应符合包括丁香假单胞菌致病变种(3)在内的LOPAT第Ia组。使用REP、ERIC和BOX引物(4)进行的重复外显子回文序列(Rep)-PCR指纹图谱分析显示,所有菌株的图谱均相同。对三个代表性菌株(每个寄主各一个)进行了管家基因gyrB和rpoD(1)的序列分型。序列分别作为登录号KM979434至KM979436(分别来自胡萝卜、防风草和欧芹的菌株)存入NCBI GenBank数据库用于gyrB基因,以及登录号KM979437至KM979439(分别来自防风草、欧芹和胡萝卜的菌株)用于rpoD基因。将序列与保存在植物相关和环境微生物数据库(http://genome.ppws.vt.edu/cgi-bin/MLST/home.pl)中的致病型菌株丁香假单胞菌芫荽致病变种ICMP12471进行比较。BLAST分析显示gyrB的同源性为100%,rpoD的同源性为99%。使用两种方法对来自每个寄主的5个代表性菌株在四周龄的胡萝卜(品种南特)、欧芹(品种NS Molski)和防风草(品种Dugi beli glatki)植株上进行致病性测试:将细菌悬浮液(10 CFU/ml)喷洒在叶片上直至径流(5),以及用皮下注射器将细菌悬浮液注入叶片(2)。每个菌株和方法使用4株植物。对每个植物品种,使用无菌蒸馏水作为阴性对照处理。所有植物在湿度为100%的雾室中放置4小时,然后转移到25°C、相对湿度80%的温室中,在三周内观察症状发展情况。对于所有菌株,接种叶片在接种后5至7天(DAI)首先在叶片上出现水渍状病斑;14 DAI时病斑变为深褐色,常被晕圈包围。接种无菌蒸馏水的对照植物未观察到症状。为满足柯赫氏法则,将重新分离的菌株接种到NAS上。从每个接种寄主中获得了重新分离出的细菌,并使用LOPAT测试和Rep-PCR指纹图谱确认其与原始分离株相同。基于致病性测试并完成柯赫氏法则、序列分析和细菌学测试,这些菌株被鉴定为丁香假单胞菌芫荽致病变种。据我们所知,这是塞尔维亚胡萝卜、欧芹和防风草细菌性叶斑病的首次报道。由于对新鲜市场的质量要求,它可能对生产构成威胁。参考文献:(1)P. Ferrente和M. Scortichini。植物病理学。59:954,2010。(2)M. Gupta等人。植物病害。97:418,2013。(3)R. A. Lelliott等人。应用细菌学杂志。29:470,1966。(4)F. J. Louws等人。应用与环境微生物学。60:2286,1994。(5)X. Xu和S. A. Miller。植物病害。97:988,2013。

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