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可可毛色二孢菌引起芒果花序疫病的首次报道。

First Report of Lasiodiplodia theobromae Causing Inflorescence Blight of Mango.

作者信息

Serrato-Diaz L M, Perez-Cuevas M, Rivera-Vargas L I, French-Monar R D

机构信息

Department of Plant Pathology and Microbiology, Texas A&M AgriLife Extension Service, Amarillo.

Department of Agronomy, University of ISA, Dominican Republic.

出版信息

Plant Dis. 2013 Oct;97(10):1380. doi: 10.1094/PDIS-03-13-0238-PDN.

Abstract

Mango (Mangifera indica L.) is an important tropical fruit crop in Puerto Rico. During a disease survey from 2008 to 2010, inflorescence blight was observed at the Mango Germplasm Collection of the University of Puerto Rico's Experiment Station in Juana Diaz as a rotting of the rachis (main axis of the inflorescence), rachilla (lateral axis), and flowers. Diseased inflorescences from cultivars 'Haden' and 'Irwin' were disinfested with 70% ethanol, followed by 0.5% sodium hypochlorite, rinsed with sterile water, and transferred to acidified potato dextrose agar (APDA). Two isolates of Lasiodiplodia theobromae (Pat.) Griffon & Maubl. were isolated from symptomatic tissue and identified morphologically using a Botryosphaeriaceae taxonomic key (3). In APDA, colonies of L. theobromae had initial greenish gray aerial mycelia that turned dark brown with age. Pycnidia were uniloculate and dark brown to black in color. Conidiogenous cells were hyaline, cylindrical, and holoblastic. Immature conidia were subovoid to ellipsoid, apex rounded, truncate at the base, thick walled, hyaline and one-celled, becoming dark brown, two-celled with irregular longitudinal striations when mature. Conidia (n = 50) averaged 26.88 μm long by 12.98 μm wide. Genomic DNA was extracted from pure cultures using a Qiagen DNeasy Plant Mini Kit. PCR amplification of three genes was used to support morphological identification. DNA analysis of the ITS1-5.8S-ITS2 region, and fragments of both β-tubulin and elongation factor 1 alpha (EF1-α) genes were sequenced and compared using BLASTN with sequences available in GenBank. Accession numbers of gene sequences of L. theobromae from Puerto Rico submitted to GenBank were: KC631659 and KC631660 for ITS region; KC631651 and KC631652 for β-tubulin; and KC631655 and KC631656 for EF1α. For all genes used, sequences were 99 to 100% identical to reference isolate CBS164.96 of L. theobromae reported in GenBank. Pathogenicity tests were conducted on six random healthy non-detached mango inflorescences from cultivars Haden and Irwin. Inflorescences were inoculated with 5-mm mycelial disks from 8-day-old pure cultures grown in APDA and kept in a humid chamber using plastic bags for 8 days under field conditions. Untreated controls were inoculated with APDA disks only. The test was repeated twice. For both cultivars, isolates of L. theobromae caused inflorescence (rachis, rachilla, and flowers) blight, 8 days after inoculation. Inflorescences turned brown and profuse mycelial growth was observed on the inflorescences. Untreated controls were disease-free and no fungi were reisolated from tissue. L. theobromae was reisolated from diseased inflorescences, fulfilling Koch's postulates. Fungi in the family Botryosphaeriaceae have been associated with stem-end rot, fruit rot, branch dieback, blossom blight, and cankers on mango (1,2,4). Worldwide, L. theobromae has only been reported causing dieback, stem end rot and fruit rot in mango (1,2). To our knowledge, this is the first report of L. theobromae causing inflorescence blight in mango. References: (1) N. I. Hui-Fang et al. Botanical Stud. 53:467, 2012. (2) A. M. Ismail et al. Australas. Plant Pathol. 41:649, 2012. (3) A. J. L. Phillips. Key to the various lineages in "Botryosphaeria" Version 01 2007. Retrieved from http://www.crem.fct.unl.pt/botryosphaeria_site/key.htm , 6 August 2013. (4) B. Slippers et al. Mycologia 97:99, 2005.

摘要

芒果(Mangifera indica L.)是波多黎各一种重要的热带水果作物。在2008年至2010年的病害调查期间,在位于胡安娜迪亚斯的波多黎各大学实验站的芒果种质资源库中观察到花序枯萎病,表现为穗轴(花序主轴)、小穗轴(侧轴)和花朵腐烂。来自‘哈登’和‘欧文’品种的患病花序先用70%乙醇进行消毒,然后用0.5%次氯酸钠处理,再用无菌水冲洗,之后转移到酸化马铃薯葡萄糖琼脂(APDA)上。从有症状的组织中分离出两株可可毛色二孢(Lasiodiplodia theobromae (Pat.) Griffon & Maubl.)菌株,并使用葡萄座腔菌科分类检索表进行形态学鉴定(3)。在APDA上,可可毛色二孢的菌落最初有绿色灰色气生菌丝体,随着时间推移会变成深褐色。分生孢子器单腔,颜色从深褐色到黑色。产孢细胞透明,圆柱形,全壁芽生式产孢。未成熟分生孢子近卵形至椭圆形,顶端圆形,基部截形,壁厚,透明且单细胞,成熟时变为深褐色,双细胞且有不规则纵向条纹。分生孢子(n = 50)平均长26.88μm,宽12.98μm。使用Qiagen DNeasy植物微量提取试剂盒从纯培养物中提取基因组DNA。对三个基因进行PCR扩增以支持形态学鉴定。对ITS1 - 5.8S - ITS2区域以及β - 微管蛋白和延伸因子1α(EF1 - α)基因的片段进行测序,并使用BLASTN与GenBank中可用的序列进行比较。提交到GenBank的来自波多黎各的可可毛色二孢基因序列登录号为:ITS区域的KC631659和KC631660;β - 微管蛋白的KC631651和KC631652;EF1α的KC631655和KC631656用于所有使用的基因,序列与GenBank中报道的可可毛色二孢参考菌株CBS164.96的序列相似度为99%至100%。对来自‘哈登’和‘欧文’品种的六个随机选取的健康未分离芒果花序进行致病性测试。花序用在APDA上培养8天的纯培养物的5毫米菌丝圆盘接种,并在田间条件下使用塑料袋在潮湿箱中放置8天。未处理的对照仅接种APDA圆盘。该试验重复两次。对于两个品种,可可毛色二孢菌株在接种8天后都导致了花序(穗轴、小穗轴和花朵)枯萎。花序变成褐色,并且在花序上观察到大量菌丝生长。未处理的对照没有病害,并且没有从组织中重新分离出真菌。从患病花序中重新分离出可可毛色二孢,满足柯赫氏法则。葡萄座腔菌科的真菌与芒果的果柄端腐病、果实腐烂、枝条枯死、花枯萎病和溃疡病有关(1,2,4)。在世界范围内,可可毛色二孢仅被报道在芒果中引起枝条枯死、果柄端腐病和果实腐烂(1,2)。据我们所知,这是可可毛色二孢引起芒果花序枯萎病的首次报道。参考文献:(1)N. I. Hui - Fang等人,《植物学研究》53:467,2012年。(2)A. M. Ismail等人,《澳大利亚植物病理学》41:649,2012年。(3)A. J. L. Phillips,《“葡萄座腔菌属”各谱系检索表》版本01 2007。从http://www.crem.fct.unl.pt/botryosphaeria_site/key.htm获取,2013年8月6日。(4)B. Slippers等人,《真菌学》97:99,2005年。

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