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中国可可毛色二孢引起柚子果实腐烂病的首次报道。

First Report of Fruit Rot Disease on Pomelo Caused by Lasiodiplodia theobromae in China.

作者信息

Luo M, Dong Z Y, Bin S Y, Lin J T

机构信息

Department of Plant Protection, Zhongkai University of Agriculture and Engineering, Guangzhou, China 510225 and Laboratory of Plant Nematology, South China Agricultural University, Guangzhou, China 510642.

Department of Plant Protection, Zhongkai University of Agriculture and Engineering, Guangzhou, China 510225.

出版信息

Plant Dis. 2011 Sep;95(9):1190. doi: 10.1094/PDIS-03-11-0214.

Abstract

Pomelo (Citrus grandis) is widely cultivated in MeiZhou Guangdong Province of China. In 2008, a disease on pomelo fruit caused significant economic losses by affecting fruit quality. Diseased fruit was collected in December 2008 from MeiZhou Guangdong, surface sterilized in 75% ethanol for 1 min and internal necrotic tissue was transferred to potato dextrose agar (PDA) and incubated at 28°C for 5 days. Three single-spore isolates were obtained from different fruit and identified as Lasiodiplodia theobromae (Pat.) Griffon & Maubl. (synonyms Diplodia natalensis Pole-Evans and Botryodiplodia theobromae Pat.; teleomorph Botryosphaeria rhodina (Cooke) Arx) on the basis of morphological and physiological features. The fungus produced dark brown colonies (initially grayish) on PDA. Young hyphae were hyaline and aseptate, whereas mature hyphae were septate with irregular branches. Cultures of L. theobromae produced globular or irregular pycnidia abundantly on PDA (pH 3.5) at 28°C after 1 month. Mature conidia of L. theobromae were 20 to 26 × 12 to 15.5 μm, subovoid to ellipsoid-ovoid, initially hyaline and nonseptate, remaining hyaline for a long time, and finally becoming dark brown and one septate with melanin deposits on the inner surface of the wall arranged longitudinally giving a striate appearance to the conidia. The internal transcribed spacer (ITS) region of the rDNA was amplified from gDNA using primers ITS1 (5'-TCCGATGGTGAACCTGCGG-3') and ITS4 (5'-TCCTCCGCTTATTGATATGC-3') (1). Amplicons were 542 bp long (GenBank Accession No. JF693024) and had 100% nucleotide identity with the corresponding sequence (GenBank Accession No. EU860391) of L. theobromae isolated from a Pinus sp. (2). To satisfy Koch's postulates, six asymptomatic fruit on potted plants were sprayed until runoff with a spore suspension (1 × 10 spores/ml) prepared from 30-day-old cultures of one isolate. Control fruit received water. Plants were covered with sterile wet gauze to maintain high humidity. Fruit spot symptoms similar to those on diseased field fruit appeared after 15 days on all inoculated fruits. L. theobromae was reisolated from all inoculated test fruit. No symptoms were observed on the fruit of control plants. To our knowledge, this is the first report of L. theobromae causing disease on pomelo fruit in China. This pathogen has also been previously reported to be economically important on a number of other hosts by mostly affecting the leaves. References: (1) J. C. Batzer et al. Mycologia 97:1268, 2005. (2) C. A. Pérez et al. Fungal Divers. 41:53,2010.

摘要

柚(Citrus grandis)在中国广东省梅州市广泛种植。2008年,一种影响柚果实品质的病害造成了重大经济损失。2008年12月从广东梅州采集患病果实,在75%乙醇中表面消毒1分钟,将内部坏死组织转移至马铃薯葡萄糖琼脂(PDA)上,于28°C培养5天。从不同果实中获得了三个单孢分离物,根据形态和生理特征鉴定为可可毛色二孢(Lasiodiplodia theobromae (Pat.) Griffon & Maubl.)(同义词:纳塔尔色二孢(Diplodia natalensis Pole-Evans)和可可葡萄座腔菌(Botryodiplodia theobromae Pat.);有性型为可可球座菌(Botryosphaeria rhodina (Cooke) Arx))。该真菌在PDA上产生深褐色菌落(最初为灰色)。幼嫩菌丝无色且无隔膜,而成熟菌丝有隔膜且具不规则分支。在28°C下培养1个月后,可可毛色二孢的培养物在PDA(pH 3.5)上大量产生球形或不规则的分生孢子器。可可毛色二孢的成熟分生孢子大小为20至26×12至15.5μm,近卵形至椭圆卵形,最初无色且无隔膜,长时间保持无色,最终变为深褐色且具一个隔膜,在隔膜内壁有纵向排列的黑色素沉积,使分生孢子呈现条纹状外观。使用引物ITS1(5'-TCCGATGGTGAACCTGCGG-3')和ITS4(5'-TCCTCCGCTTATTGATATGC-3')从基因组DNA中扩增rDNA的内部转录间隔区(ITS)区域(1)。扩增片段长542bp(GenBank登录号:JF693024),与从松属植物分离的可可毛色二孢的相应序列(GenBank登录号:EU860391)具有100%的核苷酸同一性(2)。为了满足柯赫氏法则,用从一个分离物的30天龄培养物制备的孢子悬浮液(1×10个孢子/ml)对盆栽植物上的六个无症状果实进行喷雾直至径流。对照果实喷水。用无菌湿纱布覆盖植株以保持高湿度。接种后15天,所有接种果实上均出现了与患病田间果实相似的果斑症状。从所有接种的试验果实中重新分离到了可可毛色二孢。对照植株的果实未观察到症状。据我们所知,这是可可毛色二孢在中国引起柚果实病害的首次报道。此前也有报道称该病原菌对许多其他寄主具有经济重要性,主要影响叶片。参考文献:(1)J.C. Batzer等人,《真菌学》97:1268,2005年。(2)C.A. Pérez等人,《真菌多样性》41:53,2010年。

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