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美国首次报道立枯丝核菌AG2-2IIIB侵染马铃薯茎和匍匐茎

First Report of Rhizoctonia solani AG2-2IIIB Infecting Potato Stems and Stolons in the United States.

作者信息

Woodhall J W, Belcher A R, Peters J C, Kirk W W, Wharton P S

机构信息

The Food and Environment Research Agency, Sand Hutton, York, YO41 1LZ, UK.

Aberdeen Research and Extension Center, University of Idaho, Aberdeen, ID, 83210.

出版信息

Plant Dis. 2012 Mar;96(3):460. doi: 10.1094/PDIS-10-11-0899.

Abstract

Rhizoctonia solani is an important pathogen of potato (Solanum tuberosum) causing qualitative and quantitative losses. It has been associated with black scurf and stem canker. Isolates of the fungus are assigned to one of 13 known anastomosis groups (AGs), of which AG3 is most commonly associated with potato disease (2,4). In August 2011, diseased potato plants originating from Rupert, ID (cv. Western Russet) and Three Rivers, MI (cv. Russet Norkotah) were received for diagnosis. Both samples displayed stem and stolon lesions typically associated with Rhizoctonia stem canker. The presence of R. solani was confirmed through isolation as previously described (4) and the Idaho and Michigan isolates were designated J11 and J8, respectively. AG was determined by sequencing the rDNA internal transcribed spacer (ITS) region using primers ITS5 and ITS4 (3). The resulting sequences of the rDNA ITS region of isolates J8 and J11 (GenBank Accession Nos. HE608839 and HE608840, respectively) were between 97 and 100% identical to that of other AG2-2IIIB isolates present in sequence databases (GenBank Accession Nos. FJ492075 and FJ492170, respectively). Koch's postulates were confirmed for each isolate by carrying out the following protocol. Each isolate was cultured on potato dextrose agar for 14 days. Five 10-mm agar plugs were then placed on top of seed tubers (cv. Maris Piper) in 1-liter pots containing John Innes Number 3 compost (John Innes Manufacturers Association, Reading, UK). Pots were held in a controlled environment room at 18°C with 50% relative humidity and watered as required. After 21 days, plants were removed and assessed for disease. Typical Rhizoctonia stem lesions were observed and R. solani was successfully reisolated from symptomatic material. To our knowledge, this is the first report of AG2-2IIIB causing disease on potatoes in the United States. In the United States, AGs 2-1, 3, 4, 5, and 9 have all been previously implicated in Rhizoctonia potato disease (2). AG2-2IIIB should now also be considered a potato pathogen in the United States. Knowledge of which AG is present is invaluable when considering a disease management strategy. AG2-2IIIB is a causal agent of sugar beet (Beta vulgaris) root rot in Idaho (1). Sugar beet is commonly grown in crop rotation with potato and such a rotation could increase the risk of soilborne infection to either crop by AG2-2IIIB. References: (1) C. A. Strausbaugh et al. Can. J. Plant Pathol. 33:210, 2011. (2) L. Tsror. J. Phytopatol. 158:649, 2010. (3) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. M. A. Innis et al., eds. Academic Press, Inc., New York, 1990. (4) J. W.Woodhall et al. Plant Pathol. 56:286, 2007.

摘要

立枯丝核菌是马铃薯(Solanum tuberosum)的一种重要病原菌,会造成质量和产量损失。它与黑痣病和茎溃疡病有关。该真菌的分离株被归为13个已知的融合群(AGs)之一,其中AG3最常与马铃薯病害相关(2,4)。2011年8月,收到了来自爱达荷州鲁珀特(品种:西部褐皮)和密歇根州三河(品种:褐皮诺科塔)的患病马铃薯植株进行诊断。两个样本均表现出典型的与立枯丝核菌茎溃疡病相关的茎和匍匐茎病变。通过如前所述的分离方法(4)确认了立枯丝核菌的存在,爱达荷州和密歇根州的分离株分别被命名为J11和J8。使用引物ITS5和ITS4通过对核糖体DNA内转录间隔区(ITS)区域进行测序来确定AG(3)。分离株J8和J11的核糖体DNA ITS区域的所得序列(GenBank登录号分别为HE608839和HE608840)与序列数据库中存在的其他AG2 - 2IIIB分离株(GenBank登录号分别为FJ492075和FJ492170)的序列有97%至100%的同一性。通过执行以下方案对每个分离株进行了柯赫氏法则验证。每个分离株在马铃薯葡萄糖琼脂上培养14天。然后将五个10毫米的琼脂块放置在装有约翰英尼斯3号堆肥(约翰英尼斯制造商协会,英国雷丁)的1升花盆中的种薯(品种:马里斯派珀)顶部。花盆放置在温度为18°C、相对湿度为50%的可控环境室中,并根据需要浇水。21天后,将植株移出并评估病害情况。观察到典型的立枯丝核菌茎部病变,并且从有症状的材料中成功重新分离出立枯丝核菌。据我们所知,这是AG2 - 2IIIB在美国导致马铃薯病害的首次报道。在美国,AG2 - 1、3、4、5和9此前均与立枯丝核菌马铃薯病害有关(2)。现在AG2 - 2IIIB在美国也应被视为马铃薯病原菌。在考虑病害管理策略时,了解存在哪种AG非常重要。AG2 - 2IIIB是爱达荷州甜菜(Beta vulgaris)根腐病的病原菌之一(1)。甜菜通常与马铃薯轮作种植,这样的轮作可能会增加AG2 - 2IIIB对两种作物造成土传感染的风险。参考文献:(1)C. A. Strausbaugh等人,《加拿大植物病理学杂志》33:210,2011年。(2)L. Tsror,《植物病理学杂志》158:649,2010年。(3)T. J. White等人,载于《PCR协议:方法与应用指南》。M. A. Innis等人编。学术出版社,纽约,1990年,第315页。(4)J. W. Woodhall等人,《植物病理学》56:286,2007年。

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