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短小新壳梭孢菌引起波多黎各芒果(杧果)穗轴坏死的首次报道

First Report of Neofusicoccum parvum Causing Rachis Necrosis of Mango (Mangifera indica) in Puerto Rico.

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):1381. doi: 10.1094/PDIS-03-13-0291-PDN.

Abstract

Mango is an important tropical fruit crop in Puerto Rico that has been grown in the island for centuries. One of the major disease issues in mango production is rotting of the rachis (main axis stem of the inflorescence). During a disease survey from 2008 to 2010, rachis and flower necrosis were observed at the Mango Germplasm Collection of the University of Puerto Rico's Experiment Station in Juana Diaz. Diseased inflorescences from cultivars Haden and Irwin were disinfested with 70% ethanol, followed by 0.5% sodium hypochlorite, rinsed with sterile, deionized, double-distilled water, and transferred to acidified potato dextrose agar (APDA). Two isolates, 91LY and K15C, of Neofusicoccum parvum (Pennycook & Samuels) Crous, Slippers & A.J.L. were purified and identified morphologically using taxonomic keys (1,4) and DNA sequence comparisons. In APDA, colonies of N. parvum were whitish grey with aerial mycelia turning dark gray with age. Pycnidia were uni- or multilocular and dark brown to black in color. Conidiogenous cells were hyaline and holoblastic. Conidia were hyaline, ellipsoid, smooth, and one-celled with sub-obtuse apex and truncate base. Conidia (n = 50) were 16.75 μm long by 5.5 μm wide. PCR amplification of three genes was used to support morphological identification. DNA analysis of 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 other sequences of N. parvum submitted to the NCBI GenBank. Accession numbers of gene sequences of N. parvum submitted to GenBank were: KC631661 and KC631662 for ITS region; KC631653 and KC631654 for β-tubulin; and KC631657 and KC631658 for EF1-α. For all genes used, sequences were 99 to 100% identical to ex-type specimen CMW9081 of N. parvum reported in GenBank. Pathogenicity tests were conducted on mango trees using six random healthy non-detached mango inflorescences for both Haden and Irwin cultivars and for both isolates. 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 temperature, light, and other environmental conditions. Untreated controls were inoculated with APDA disks only. The test was repeated twice. For both cultivars, at 8 days after inoculation, isolates of N. parvum caused rachis necrosis ranging from 20 to 35 mm in rachis length. On cultivar Irwin, inflorescences turned brown and the necrosis was extended from the rachis to the flowers. On cultivar Haden, inflorescences turned brown and only rachis necrosis was observed. Untreated controls showed no symptoms and no fungi were reisolated from tissue. N. parvum was reisolated from diseased inflorescences, fulfilling Koch's postulates. Worldwide, N. parvum has been associated with stem-end rot, branch dieback, blossom blight, and cankers on mango (2,3). To our knowledge, this is the first report of N. parvum causing rachis necrosis on mango in Puerto Rico. References: (1) 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. (2) G. I. Johnson et al. Ann. Appl. Biol. 120:225, 1992. (3) B. Slippers et al. Mycologia 97:99, 2005. (4) P. W. Crous et al. Stud. Mycol. 55:235, 2006.

摘要

芒果是波多黎各一种重要的热带水果作物,在该岛已种植了几个世纪。芒果生产中的一个主要病害问题是果轴(花序的主轴茎)腐烂。在2008年至2010年的病害调查中,在波多黎各胡安娜迪亚斯大学实验站的芒果种质资源库中观察到果轴和花朵坏死现象。对哈顿和欧文品种的染病花序先用70%乙醇进行消毒,再用0.5%次氯酸钠处理,然后用无菌去离子双蒸水冲洗,并转移至酸化马铃薯葡萄糖琼脂(APDA)培养基上。对两种细小新壳梭孢(Neofusicoccum parvum (Pennycook & Samuels) Crous, Slippers & A.J.L.)分离株91LY和K15C进行了纯化,并使用分类学检索表(1,4)和DNA序列比较进行形态学鉴定。在APDA培养基上,细小新壳梭孢的菌落呈灰白色,气生菌丝体随着生长变为深灰色。分生孢子器单腔或多腔,颜色为深褐色至黑色。产孢细胞透明,全壁芽生式产孢。分生孢子透明,椭圆形,表面光滑,单细胞,顶端近钝形,基部截形。分生孢子(n = 50)长16.75μm,宽5.5μm。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1-α(EF1-α)基因的片段进行DNA分析,测序后使用BLASTn与提交至NCBI GenBank的其他细小新壳梭孢序列进行比较。提交至GenBank的细小新壳梭孢基因序列登录号为:ITS区域的KC631661和KC631662;β-微管蛋白的KC631653和KC631654;EF1-α的KC631657和KC631658。对于所有使用的基因,其序列与GenBank中报道的细小新壳梭孢模式菌株CMW9081的序列相似度为99%至100%。使用哈顿和欧文两个品种的六个随机选取的健康未分离芒果花序,对两种分离株进行芒果树致病性测试。花序接种来自在APDA培养基上生长8天的纯培养物的5mm菌丝盘,并在田间温度、光照和其他环境条件下,使用塑料袋在潮湿箱中放置8天。未处理的对照仅接种APDA盘。该试验重复两次。对于两个品种,接种后8天,细小新壳梭孢分离株导致果轴坏死,果轴长度坏死范围为20至35mm。在欧文品种上,花序变为褐色,坏死从果轴扩展到花朵。在哈顿品种上,花序变为褐色,仅观察到果轴坏死。未处理的对照未出现症状,且未从组织中重新分离到真菌。从染病花序中重新分离到细小新壳梭孢,满足柯赫氏法则。在全球范围内,细小新壳梭孢与芒果的果柄端腐病、枝条枯死、花腐病和溃疡病有关(2,3)。据我们所知,这是关于细小新壳梭孢在波多黎各导致芒果果轴坏死的首次报道。参考文献:(1)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. (2)G. I. Johnson et al. Ann. Appl. Biol. 120:225, 1992. (3)B. Slippers et al. Mycologia 97:99, 2005. (4)P. W. Crous et al. Stud. Mycol. 55:235, 2006.

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