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美国首次报道石榴生壳囊孢菌引起石榴( Punica granatum)木溃疡和枝条枯死病 。

First Report of Cytospora punicae Causing Wood Canker and Branch Dieback of Pomegranate (Punica granatum) in the United States.

作者信息

Peduto Hand F, Choudhury R A, Gubler W D

机构信息

Department of Plant Pathology, The Ohio State University, 2021 Coffey Road, Columbus, OH 43210.

Department of Plant Pathology, University of California Davis, One Shields Avenue, Davis, CA 95616.

出版信息

Plant Dis. 2014 Jun;98(6):853. doi: 10.1094/PDIS-11-13-1133-PDN.

Abstract

Pomegranates (Punica granatum L.) are an expanding industry in the United States with California growing approximately 32,000 acres with a crop value of over $155 million (1). During June and July of 2012, we observed severe limb and branch dieback in pomegranate orchards cv. Wonderful located in Contra Costa, Kings, and Kern counties of California. Disease symptoms included yellowing of leaves, branch and limb dieback, wood lesions, and canker formation. Dark brown Cytospora-like cultures were consistently isolated from active cankers on potato dextrose agar (PDA) amended with 100 mg l tetracycline hydrochloride. Three isolates (UCCE1223, UCCE1233, and UCCE1234) representative of each orchard were sub-cultured onto PDA and incubated at 22°C under fluorescent intermittent light (12 h light, 12 h dark). Fungal colonies had whitish mycelia that turned olive green to dark brown with maturity and formed globose and dark brown pycnidia after 12 days. Conidia were hyaline, aseptate, allantoid, and (4) 4.5 to 5 (6) × (1) 1.5 (2) μm (n = 180). Pycnidia formed in culture measured (250) 350 to 475 (650) μm in diameter (n = 40). Identification of the isolates was confirmed by sequence comparison of the internal transcribed spacer region (ITS1-5.8S-ITS2) of the rDNA and part of the translation elongation factor 1-α gene (EF1-α) with sequences available in GenBank. Consensus sequences of both genes of all isolates showed 99% homology to the species Cytospora punicae Sacc. (2). All sequences were deposited in GenBank (Accession Nos. KJ621684 to 89). Pathogenicity of the isolates was determined by branch inoculation. In December 2012, 3-year-old branches of P. granatum cv. Wonderful were inoculated by placing 5-mm-diameter mycelium plugs from the growing margin of 14-day-old PDA cultures in fresh wounds made with a 5-mm-diameter cork-borer. Eight branches per isolate were inoculated on eight different trees. Eight control branches were inoculated with non-colonized PDA agar plugs. Inoculations were covered with Vaseline and wrapped with Parafilm to retain moisture. Branches were harvested in August 2013 and examined for canker development and the extent of vascular discoloration spreading downward and upward from the inoculation point. Isolations from the edge of discolored tissue were conducted to fulfill Koch's postulates. C. punicae was re-isolated from 100% of the inoculated branches. Total length of vascular discoloration averaged 30.2 mm in branches inoculated with the three C. punicae isolates and 9 mm in the control branches. No fungi were isolated from the slightly discolored tissue of the controls. To our knowledge, this is the first report of C. punicae as a fungal trunk pathogen of pomegranate trees in the United States. References: (1) California County Agricultural Commissioners' Data, 2010 Crop Year. USDA NASS California field office, retrieved from http://www.nass.usda.gov/Statistics_by_State/California/ Publications/AgComm/201010cactb00.pdf , 2011. (2) P. A. Saccardo. Sylloge Fungorum 3:256, 1884.

摘要

石榴(Punica granatum L.)在美国是一个不断发展的产业,加利福尼亚州种植面积约32000英亩,作物产值超过1.55亿美元(1)。2012年6月和7月,我们在加利福尼亚州康特拉科斯塔县、金斯县和克恩县的“奇妙”品种石榴果园中观察到严重的枝干枯死现象。病害症状包括叶片发黄、枝干枯死、木质部病变和溃疡形成。在添加了100 mg/l盐酸四环素的马铃薯葡萄糖琼脂(PDA)上,从活跃的溃疡部位持续分离出深褐色的似壳囊孢属培养物。从每个果园选取三个代表性分离株(UCCE1223、UCCE1233和UCCE1234)转接至PDA上,并在22°C、荧光间歇光照(12小时光照,12小时黑暗)条件下培养。真菌菌落有白色菌丝体,成熟后变为橄榄绿至深褐色,12天后形成球形深褐色分生孢子器。分生孢子无色、无隔膜、腊肠形,大小为(4)4.5至5(6)×(1)1.5(2)μm(n = 180)。培养形成的分生孢子器直径为(250)350至475(650)μm(n = 40)。通过将rDNA的内部转录间隔区(ITS1 - 5.8S - ITS2)和翻译延伸因子1 - α基因(EF1 - α)的部分序列与GenBank中可用序列进行比较,确认了分离株的身份。所有分离株这两个基因的一致序列与石榴壳囊孢菌(Cytospora punicae Sacc.)的序列显示出99%的同源性(2)。所有序列均已存入GenBank(登录号:KJ621684至89)。通过枝条接种测定分离株的致病性。2012年12月,用直径5 mm的打孔器在“奇妙”品种3年生石榴树枝条上造成新鲜伤口,然后将14天龄PDA培养物生长边缘的直径5 mm菌丝块接种到伤口处。每个分离株接种8个枝条,接种在8棵不同的树上。8个对照枝条接种未被污染的PDA琼脂块。接种部位用凡士林覆盖,并用保鲜膜包裹以保持湿度。2013年8月收获枝条,检查溃疡发展情况以及从接种点向下和向上蔓延的维管束变色程度。从变色组织边缘进行分离以验证柯赫氏法则。从100%接种的枝条中再次分离出石榴壳囊孢菌。接种三个石榴壳囊孢菌分离株的枝条中维管束变色的总长度平均为30.2 mm,对照枝条中为9 mm。对照枝条轻微变色的组织中未分离到真菌。据我们所知,这是石榴壳囊孢菌作为美国石榴树真菌性树干病原菌的首次报道。参考文献:(1)加利福尼亚州县农业专员数据,2010作物年度。美国农业部国家农业统计局加利福尼亚州办公室,从http://www.nass.usda.gov/Statistics_by_State/California/ Publications/AgComm/201010cactb00.pdf获取,2011年。(2)P. A. 萨卡尔多。真菌汇刊3:256,1884年。

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