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纽约大豆上由菜豆壳球孢引起的炭腐病首次报道

First Report of Charcoal Rot Caused by Macrophomina phaseolina in Soybean in New York.

作者信息

Cummings J A, Bergstrom G C

机构信息

Department of Plant Pathology and Plant-Microbe Biology, Cornell University, Ithaca 14853-5904.

出版信息

Plant Dis. 2013 Nov;97(11):1506. doi: 10.1094/PDIS-03-13-0318-PDN.

Abstract

Charcoal rot of soybean (Glycine max (L.) Merr.), incited by Macrophomina phaseolina (Tassi) Goidanich, is commonly found in much of the southern soybean production region of the United States, where it can be a major contributor to yield loss in warm, dry seasons (4). The disease has also been reported in northern states including Michigan, Minnesota, North Dakota, and Wisconsin (1,2,3). In early July of the warmer and drier than normal 2012 growing season, wilted soybean plants were observed and collected for diagnosis from a field in Cayuga County, NY. The diseased plants showed brown discoloration of the stem and roots but the diagnostic microsclerotia of M. phaseolina had not yet developed in the epidermis. Cut pieces of roots and crowns were surface-sterilized in 20% sodium hypochlorite, rinsed in sterile distilled water, and incubated on potato dextrose agar at room temperature with a 12-h photoperiod for 7 days. The pathogen was observed growing out of many of the crown and root pieces, and produced abundant microsclerotia as described by Smith and Wyllie (4). Pathogenicity of isolate Mp001NY12 was confirmed using a cut stem inoculation method. Five soybean plants were grown to the unifoliate stage and inoculated by cutting the stem above the unifoliate leaves and applying a fully colonized agar plug to the wound. Within 2 weeks, infection was obvious with microsclerotia formed in the epidermis of all infected plants, and M. phaseolina was reisolated from all infected plants. DNA of isolate Mp001NY12 was extracted from colonies grown on PDA with PrepMan Ultra DNA extraction kit (Applied Biosystems, Foster City, CA), and the DNA was submitted for ITS sequencing with the ITS1 and ITS4 primers used for PCR amplification. The ITS sequence (GenBank Accession No. KC800709) of Mp001NY12 was compared to those in the NCBI GenBank database using a BLAST search, and had 99% nucleotide sequence identity with M. phaseolina (accessions JX945170, FJ415067, and EU250575). To the best of our knowledge, charcoal rot has not been reported previously on soybean or other plant hosts in New York or in other states in the northeastern United States. References: (1) Baird et al. Mycopathologia 170:169, 2010. (2) C. A. Bradley and L. E. del Rio. Plant Dis. 87:601, 2003. (3) M. E. ElAraby et al. Plant Dis. 87:202, 2003. (4) G. S. Smith and T. D. Wyllie. Charcoal rot. Page 29 in: Compendium of Soybean Diseases, 4th ed. G. L. Hartman et al., eds. APS Press, St. Paul, MN, 1999.

摘要

由菜豆壳球孢菌(Macrophomina phaseolina (Tassi) Goidanich)引起的大豆炭腐病,在美国南部大部分大豆产区普遍存在,在温暖干燥的季节,它可能是导致产量损失的主要因素(4)。在包括密歇根州、明尼苏达州、北达科他州和威斯康星州在内的北部各州也有该病的报道(1,2,3)。在2012年生长季比正常情况更温暖干燥的7月初,纽约州卡尤加县的一块田地里发现了枯萎的大豆植株并采集进行诊断。患病植株的茎和根出现褐色变色,但菜豆壳球孢菌的诊断性小菌核尚未在表皮形成。将根和冠的切段在20%次氯酸钠中进行表面消毒,用无菌蒸馏水冲洗,然后在室温下、12小时光周期的条件下,在马铃薯葡萄糖琼脂上培养7天。观察到病原菌从许多冠和根切段上生长出来,并如史密斯和威利(4)所述产生了大量小菌核。使用茎切段接种法证实了分离株Mp001NY12的致病性。将五株大豆植株培育到单叶期,通过在单叶上方切断茎并在伤口处放置一个完全定殖的琼脂块进行接种。两周内,感染明显,所有感染植株的表皮都形成了小菌核,并且从所有感染植株中重新分离出了菜豆壳球孢菌。使用PrepMan Ultra DNA提取试剂盒(应用生物系统公司,加利福尼亚州福斯特城)从在PDA上生长的菌落中提取分离株Mp001NY12的DNA,并使用用于PCR扩增的ITS1和ITS4引物将该DNA提交进行ITS测序。使用BLAST搜索将Mp001NY12的ITS序列(GenBank登录号KC800709)与NCBI GenBank数据库中的序列进行比较,发现它与菜豆壳球孢菌(登录号JX945170、FJ415067和EU250575)具有99%的核苷酸序列同一性。据我们所知,此前纽约州或美国东北部其他州的大豆或其他植物寄主上尚未报道过炭腐病。参考文献:(1)贝尔德等人。《真菌病理学》170:169,2010。(2)C.A.布拉德利和L.E.德尔里奥。《植物病害》87:601,2003。(3)M.E.埃拉拉比等人。《植物病害》87:202,2003。(4)G.S.史密斯和T.D.威利。《炭腐病》。载于:《大豆病害简编》第4版。G.L.哈特曼等人编。美国植物病理学会出版社,明尼苏达州圣保罗,1999年,第29页。

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