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链格孢菌引起西班牙萝卜黑斑病的首次报道。

First Report of Alternaria japonica Causing Black Spot of Turnip in Spain.

作者信息

Bassimba D D M, Mira J L, Vicent A

机构信息

Centro de Protección Vegetal y Biotecnología, Instituto Valenciano de Investigaciones Agrarias (IVIA), Moncada 46113, Valencia, Spain.

出版信息

Plant Dis. 2013 Nov;97(11):1505. doi: 10.1094/PDIS-01-13-0090-PDN.

Abstract

Turnip (Brassica rapa subsp. rapa L.) is an annual vegetable crop cultivated for consumption of its succulent root. In July 2011, symptoms consisting of leaf spots 1 to 8 mm in diameter with a dark brown color surrounded by a yellow halo and black sunken lesions in the swollen storage root were observed in production areas in Alicante Province in east-central Spain. Disease incidence was approximately 20% in fields of about 3 ha where infection was highest. Symptomatic leaves and roots collected from turnip cv. Virtudes-Martillo in three affected fields were surface disinfected with 0.5% NaOCl for 2 min, and small fragments from necrotic lesions were plated on potato dextrose agar (PDA) amended with 0.5 g streptomycin sulfate per liter. Alternaria colonies were consistently isolated from affected leaves and roots after 7 days of incubation at 24°C, and were transferred to V-8 with autoclaved turnip cv. Virtudes-Martillo leaves. Two isolates from leaves and two isolates from roots were included in the study. Plates were incubated for 15 days at 24°C with an 8-h fluorescent light period and a 12-h dark period for morphological examination. Conidia produced in culture were mostly solitary or in short chains of 2 to 3 spores, beakless, ovoid to ellipsoid, and light brown. Conidia were 32 to 78 × 13 to 24 μm, with 3 to 7 transverse septa and 1 to 2 longisepta. Aggregated hyphal chains of dark, thick-walled ornamented cells distinctive of Alternaria japonica Yoshii (3) were observed. The 5.8S, ITS2, and 28S ribosomal RNA (rRNA) regions were amplified using the primers ITS3 and ITS4 (4) and sequenced from DNA extracted from the isolate designated as IVIA-A070, obtained from turnip leaves cv. Virtudes-Martillo in Alicante Province (GenBank Accession No. JX983044). The sequence had 100% identity (total score 302, 73% coverage) with that of A. japonica strain ATCC 13618 (2) (AY376639). Pathogenicity tests were performed twice on two 3-month-old plants of turnip cv. Virtudes-Martillo and cv. Blanco-Globo, and cabbage (B. oleracea var. capitata L.) cv. Brunswick. Plants were inoculated by spraying a conidial suspension of the isolate IVIA-A070 (10 ml/plant, 10 conidia/ml water) using manual pressure sprayer. Two plants of each host sprayed with sterile distilled water were used as controls in each experiment. Plants were covered with black plastic bags and incubated in a growth chamber for 48 h at 25°C. Leaf spots similar to those observed in affected plants in the field were visible on all turnip and cabbage plants 4 days after inoculation with the fungus. No symptoms were observed on control plants. Fungal colonies morphologically identified as A. japonica were reisolated from leaf lesions on inoculated turnip and cabbage plants, but not from asymptomatic leaves of control plants. Based on these results, the disease was identified as black spot of turnip caused by A. japonica. In Spain, black spot of brassicas was previously associated only with A. brassicae (Berkeley) Saccardo and A. brassicicola (Schw.) Wiltshire (1). References: (1) P. Melgarejo et al. Patógenos de Plantas Descritos en España. MARM-SEF, Madrid, 2010. (2) B. M. Pryor and R. L. Gilbertson. Mycol. Res. 104:1312, 2000. (3) E. G. Simmons. Alternaria: An Identification Manual. CBS Fungal Biodiversity Centre, Utrecht, 2007. (4) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, 1990.

摘要

芜菁(Brassica rapa subsp. rapa L.)是一种一年生蔬菜作物,种植目的是食用其多汁的根部。2011年7月,在西班牙中东部阿利坎特省的产区,观察到芜菁出现症状,叶片上有直径1至8毫米的病斑,呈深褐色,周围有黄色晕圈,在肿胀的贮藏根上有黑色凹陷病斑。在感染最严重的约3公顷田块中,发病率约为20%。从三个受影响田块的芜菁品种Virtudes-Martillo上采集的有症状叶片和根部,用0.5%次氯酸钠进行表面消毒2分钟,然后将坏死病斑的小碎片接种到每升添加0.5克硫酸链霉素的马铃薯葡萄糖琼脂(PDA)上。在24°C下培养7天后,始终从受影响的叶片和根部分离出链格孢菌落,并将其转移到添加了经高压灭菌的芜菁品种Virtudes-Martillo叶片的V-8培养基上。本研究包括从叶片分离的两个菌株和从根部分离的两个菌株。将平板在24°C下培养15天,光照8小时,黑暗12小时,以进行形态学检查。培养产生的分生孢子大多单个或形成2至3个孢子的短链,无喙,卵圆形至椭圆形,浅褐色。分生孢子大小为32至78×13至24微米,有3至7个横隔膜和1至2个纵隔膜。观察到由日本链格孢Yoshii(3)特有的深色、厚壁具纹饰细胞组成的聚集菌丝链。使用引物ITS3和ITS4(4)扩增5.8S、ITS2和28S核糖体RNA(rRNA)区域,并从从阿利坎特省芜菁品种Virtudes-Martillo叶片分离得到的编号为IVIA-A070的菌株中提取的DNA进行测序(GenBank登录号JX983044)。该序列与日本链格孢菌株ATCC 13618(2)(AY376639)的序列具有100%的同一性(总分302,覆盖率73%)。对芜菁品种Virtudes-Martillo和Blanco-Globo的两株3个月大植株以及甘蓝(B. oleracea var. capitata L.)品种Brunswick进行了两次致病性测试。使用手动压力喷雾器,通过喷洒分离株IVIA-A070的分生孢子悬浮液(10毫升/株,10个分生孢子/毫升水)对植株进行接种。每个实验中,用无菌蒸馏水喷洒的两株每个寄主植物用作对照。用黑色塑料袋覆盖植株,并在生长室中于25°C下培养48小时。接种真菌4天后,在所有芜菁和甘蓝植株上都可见到与田间受影响植株上观察到的类似的叶斑。对照植株上未观察到症状。从接种的芜菁和甘蓝植株的叶斑上重新分离出形态学上鉴定为日本链格孢的真菌菌落,但未从对照植株的无症状叶片上分离到。基于这些结果,该病害被鉴定为由日本链格孢引起的芜菁黑斑病。在西班牙,十字花科蔬菜的黑斑病以前仅与芸苔链格孢(Berkeley)Saccardo和芸苔生链格孢(Schw.)Wiltshire有关(1)。参考文献:(1)P. Melgarejo等人。《西班牙描述的植物病原菌》。MARM-SEF,马德里,2010年。(2)B. M. Pryor和R. L. Gilbertson。《真菌研究》104:1312,2000年。(3)E. G. Simmons。《链格孢:鉴定手册》。CBS真菌生物多样性中心,乌得勒支,2007年。(4)T. J. White等人。见《PCR协议:方法与应用指南》第315页。学术出版社,圣地亚哥,1990年。

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