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密歇根州胡萝卜黑腐病由萝卜链格孢引起的首次报道。

First Report of Black Rot of Carrots Caused by Alternaria radicina in Michigan.

作者信息

Saude C, Hausbeck M K

机构信息

Department of Plant Pathology, Michigan State University, East Lansing 48824-1311.

出版信息

Plant Dis. 2006 May;90(5):684. doi: 10.1094/PD-90-0684B.

Abstract

In April 2005, an Alternaria sp. was isolated from carrot (Daucus carota) roots harvested in the fall of 2004 and held at 1 to 3°C in a storage facility in Newaygo County, MI. The pathogen was readily isolated on water agar from root tissue exhibiting grayish black, sunken lesions. Morphological characteristics were noted 5 to 7 days after single-conidium cultures were established on potato dextrose agar (3). Sixteen Alternaria sp. isolates were recovered. Cultures were dark olive brown, and conidia were pigmented, ellipsoidal, and produced singly or in chains of two. Conidia were 35 to 45 μm long and 15 to18 μm in diameter, usually with three to eight transverse and one to four longitudinal septa. Pathogenicity of isolates was tested on carrot roots in the laboratory and carrot seedlings (cv. Goliath) in the greenhouse. In the laboratory, four surface-sterilized, whole carrot roots were sprayed until runoff with 2 × 10 conidia/ml of each isolate and incubated at 23 to 25°C in a moist chamber for 10 days. Controls were sprayed with sterile distilled water. Ten to fifteen days after inoculation, inoculated carrots exhibited grayish black, sunken lesions, and an Alternaria sp. was reisolated from the margin of the lesions. Controls remained healthy. In the greenhouse, seven pots containing one 2-week-old carrot seedling were watered to saturation and plants were sprayed until runoff with 2 × 10 conidia/ml for each isolate. Control plants were sprayed with sterile distilled water. After inoculation, plants were enclosed in clear plastic bags, placed under 63% woven shade cloth and watered regularly. Black lesions were observed on the foliage 7 days after inoculation, and wilt and death of plants were observed 15 to 30 days after inoculation. Alternaria sp. was reisolated from the foliage of symptomatic plants. Control plants remained healthy. DNA was extracted from all isolates, and the nuclear ribosomal internal transcribed spacer (ITS) region amplified with primers ITS4 and ITS5 and sequenced. A portion of the ITS sequence has been deposited in the NCBI database (GenBank Accession No. DQ394073). A BLAST search of the NCBI database with the ITS sequences revealed A. radicina, Accession No AY154704, as the closest match with 100% sequence similarity. In September 2005, an Alternaria sp. was isolated from black lesions on carrot roots, crowns, and foliage that were collected from fields in Newaygo and Oceana counties, MI. The recovered isolates were morphologically similar to A. radicina isolates obtained from stored carrots in April 2005. First isolated and identified on stored carrots in New York (3), A. radicina is also present in other carrot-producing areas of the United States (1) and was isolated not only from stored carrots but also from carrots in the field (2) and carrot seeds (4). To our knowledge, this is the first report of A. radicina on stored and field carrots in Michigan, which signifies a serious risk to a carrot industry that ranks among the top five in the United States. References: (1) D. F. Farr et al. Fungi on Plants and Plant Produce in the United States.The American Phytopathological Society, St. Paul, MN, 1989. (2) R. G. Grogan and W. C. Snyder. Phytopathology 42:215, 1952. (3) F. C. Meier and E. D. Eddy. Phytopathology 12:157, 1922. (4) B. M. Pryor and R. L. Gilbertson. Plant Dis. 85:18, 2001.

摘要

2005年4月,从2004年秋季收获并保存在密歇根州纽埃戈县一个储存设施中、温度为1至3°C的胡萝卜(胡萝卜属)根部分离出一种链格孢菌。该病原菌很容易从表现出灰黑色凹陷病斑的根组织中在水琼脂上分离出来。在马铃薯葡萄糖琼脂上建立单分生孢子培养物5至7天后,记录其形态特征(3)。共分离出16株链格孢菌。培养物呈深橄榄褐色,分生孢子有色素,椭圆形,单个产生或形成两个的链状。分生孢子长35至45μm,直径15至18μm,通常有三至八个横向隔膜和一至四个纵向隔膜。在实验室对胡萝卜根以及温室中的胡萝卜幼苗(品种为歌利亚)进行了分离菌株的致病性测试。在实验室中,将四个表面消毒的完整胡萝卜根用每种分离菌株的2×10分生孢子/毫升喷雾至径流,然后在23至25°C的潮湿培养箱中培养10天。对照用无菌蒸馏水喷雾。接种后10至15天,接种的胡萝卜出现灰黑色凹陷病斑,并且从病斑边缘重新分离出链格孢菌。对照保持健康。在温室中,给七个装有一株2周龄胡萝卜幼苗的花盆浇水至饱和,并用每种分离菌株的2×10分生孢子/毫升喷雾植株至径流。对照植株用无菌蒸馏水喷雾。接种后,将植株用透明塑料袋罩住,置于63%的编织遮阳网下并定期浇水。接种后7天在叶片上观察到黑色病斑,接种后15至30天观察到植株枯萎和死亡。从有症状植株的叶片中重新分离出链格孢菌。对照植株保持健康。从所有分离菌株中提取DNA,用引物ITS4和ITS5扩增核糖体DNA内部转录间隔区(ITS)并进行测序。ITS序列的一部分已存入NCBI数据库(GenBank登录号DQ394073)。用ITS序列在NCBI数据库中进行BLAST搜索,发现登录号为AY154704的萝卜链格孢是最接近的匹配,序列相似性为100%。2005年9月,从密歇根州纽埃戈县和奥齐纳县田间采集的胡萝卜根、冠和叶片上的黑色病斑中分离出一种链格孢菌。回收的分离菌株在形态上与2005年4月从储存胡萝卜中获得的萝卜链格孢分离菌株相似。萝卜链格孢最早在纽约的储存胡萝卜中分离和鉴定(3),在美国其他胡萝卜产区也有发现(1),不仅从储存胡萝卜中分离到,还从田间胡萝卜(2)和胡萝卜种子(4)中分离到。据我们所知,这是密歇根州储存和田间胡萝卜上萝卜链格孢的首次报道,这对在美国排名前五的胡萝卜产业意味着严重风险。参考文献:(1)D.F.法尔等人。美国植物和植物产品上的真菌。美国植物病理学会,明尼苏达州圣保罗,1989年。(2)R.G.格罗根和W.C.斯奈德。植物病理学42:215,1952年。(3)F.C.迈尔和E.D.埃迪。植物病理学12:157,1922年。(4)B.M.普赖尔和R.L.吉尔伯tson。植物病害85:18,2001年。

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