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韩国温室种植西葫芦上由灰葡萄孢引起的灰霉病首次报道。

First Report of Gray Mold Caused by Botrytis cinerea on Greenhouse-Grown Zucchini in Korea.

作者信息

Cheon W, Jeon Y H

机构信息

Department of Bioresource Sciences, Andong National University, Andong 760-749, Korea.

出版信息

Plant Dis. 2013 Aug;97(8):1116. doi: 10.1094/PDIS-01-13-0005-PDN.

Abstract

In the winter of 2011, greenhouse-grown zucchini (Cucurbita pepo) in Andong City, Korea, showed severe disease symptoms on fruits and dying leaves of zucchini plants that resembled gray mold disease with about 20% yield loss. Symptoms included extensive growth of mycelia and gray conidia on stem and fruit lesions. Lesions expanded rapidly under cool, humid conditions. As the disease progressed, leaves, stems, and fruits became necrotic and were covered by an abundant, soft, gray, sporulating mycelium. Diseased fruit tissue was excised and surface sterilized by immersion in 2% NaOCl for 1 min, placed on PDA (potato dextrose agar), and incubated at 22°C. Fungal colonies were initially white and became gray to brown after 72 h. Analysis of light micrographs showed the presence of elliptical conidia on PDA that was 7.5 to 16.0 μm long and 5 to 10.5 μm wide. In culture, a few, black, small and large irregular sclerotia were produced. Microsclerotia were round, spherical or irregular in shape, and ranged from 1.0 to 3.3 and 1.2 to 3.4 mm (width and length). Conidiophores were slender and branched with enlarged apical cells bearing smooth, ash-colored conidia. These morphological characteristics identified the fungus as Botrytis cinerea (1). The internal transcribed spacer (ITS) region of rDNA was amplified using the ITS1 (forward) and ITS4 (reverse) primer set (ITS1: 5'-TCCGTAGGTGAACCTGCGG-3', ITS4: 5'-TCCTCCGCTTATTGATATGC-3') and sequenced (2). BLAST analysis of the PCR product showed that the sequence had 100% identity with the nucleotide sequences for B. cinerea. Pathogenicity tests were performed by placing mycelium fragments (1 cm) of PDA cultures on zucchini fruits. Controls were treated with PDA alone. Five replicates for the inoculated and control plants were used. All fruits were covered with plastic bags and incubated in a growth chamber to maintain 90 to 100% relative humidity at 22°C. Typical symptoms appeared 2 to 6 days after inoculation. The inoculated plants developed typical gray mold symptoms with gray sporulating lesions, while controls remained healthy with no lesions. B. cinerea reisolated from the inoculated tissues was morphologically identical to the original isolates. In a cold outside (below 0°C), wet greenhouse, plants are likely to be exposed to resident Botrytis populations and if the gray mold disease occurs, it can spread on zucchini plants very fast, in 2 days to a week inside a 100 m greenhouse. Therefore, gray mold disease could have a significant impact on greenhouse production of zucchini. To our knowledge, this is the first report of B. cinerea causing gray mold of greenhouse-grown zucchini in Korea. References: (1) H. L. Barnett and B. B. Hunter. Illustrated Genera of Imperfect Fungi. Burgess Publishing Company, Minneapolis, MN, 1972. (2) T. J. White et al. PCR Protocols. Academic Press, Inc., New York, 1990.

摘要

2011年冬季,韩国安东市温室种植的西葫芦(南瓜属)在果实和叶片上出现严重病害症状,类似灰霉病,导致约20%的产量损失。症状包括在茎和果实病斑上有大量菌丝体生长和灰色分生孢子。在凉爽、潮湿的条件下,病斑迅速扩展。随着病情发展,叶片、茎和果实坏死,被大量柔软的灰色产孢菌丝体覆盖。将患病果实组织切除,浸入2%次氯酸钠中表面消毒1分钟,置于马铃薯葡萄糖琼脂(PDA)上,在22°C下培养。真菌菌落最初为白色,72小时后变为灰色至棕色。光学显微镜分析显示,PDA上存在椭圆形分生孢子,长7.5至16.0μm,宽5至10.5μm。在培养过程中,产生了一些黑色、大小不一的不规则菌核。微菌核形状为圆形、球形或不规则形,宽1.0至3.3mm,长1.2至3.4mm。分生孢子梗细长且有分支,顶端细胞膨大,着生光滑的灰白色分生孢子。这些形态特征将该真菌鉴定为灰葡萄孢(1)。使用ITS1(正向)和ITS4(反向)引物对(ITS1:5'-TCCGTAGGTGAACCTGCGG-3',ITS4:5'-TCCTCCGCTTATTGATATGC-3')扩增核糖体DNA的内部转录间隔区(ITS)并进行测序(2)。对PCR产物的BLAST分析表明,该序列与灰葡萄孢的核苷酸序列具有100%的同一性。通过将PDA培养物的菌丝体片段(1cm)放置在西葫芦果实上进行致病性测试。对照组仅用PDA处理。对接种和对照植株各进行5次重复。所有果实均用塑料袋覆盖,在生长室中培养,以在22°C下保持90%至100%的相对湿度。接种后2至6天出现典型症状。接种植株出现典型的灰霉症状,有灰色产孢病斑,而对照组保持健康,无病斑。从接种组织中重新分离出的灰葡萄孢在形态上与原始分离株相同。在寒冷的室外(低于0°C)、潮湿的温室中,植株可能会接触到常驻的灰葡萄孢菌种群,如果发生灰霉病,在100米的温室中,2天到一周内就能在西葫芦植株上迅速传播。因此,灰霉病可能对温室西葫芦生产产生重大影响。据我们所知,这是韩国首次报道灰葡萄孢引起温室种植西葫芦的灰霉病。参考文献:(1)H. L. Barnett和B. B. Hunter。《不完全真菌图鉴》。Burgess Publishing Company,明尼阿波利斯,明尼苏达州,1972年。(2)T. J. White等人。《PCR实验方案》。学术出版社,纽约,1990年。

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