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中国首次报道拟盘多毛孢菌引起山核桃(Carya cathayensis)树干病害。

First Report of Pestalotiopsis vismiae Causing Trunk Disease of Chinese Hickory (Carya cathayensis) in China.

作者信息

Liu Y J, Huang B, Wu Z H

机构信息

Anhui Provincial Key Laboratory of Microbial Pest Control, Anhui Agricultural University, Hefei 230036, China.

The Forestry Bureau of Ningguo Municipal, Ningguo 242300, China. This study was supported by the Special Fund for Forestry Scientific Research in the Public Interest (Grant No. 201204506).

出版信息

Plant Dis. 2014 Nov;98(11):1588. doi: 10.1094/PDIS-07-14-0688-PDN.

Abstract

Chinese hickory is an important forest crop in Anhui and Zhejiang provinces of China. In a survey conducted from 2010 to 2013, serious trunk disease was revealed on C. cathayensis in Ningguo city, Anhui Province. In 2013, nearly 20% of hickory orchards and 5% of hickory trees were affected in this region. Symptoms observed from May to November included dark brown bark lesions and bark cracking on trunks. Bark cracks increased in size over time (mostly more than 80 cm long), extending into the phloem and leading to extensive areas of bark loss with discoloration of the underlying xylem. In most cases, infected plants died within 2 to 4 years. Infected samples collected from 16 orchards in Nanji town and 8 orchards in Hule town were surface sterilized with 1.5% sodium hypochlorite for 2 min, plated on potato dextrose agar (PDA), and incubated at 25°C in the dark for 1 week. Eleven similar isolates were obtained from diseased trunks. Colonies reached 7.5 cm diameter after 7 days on PDA at 25°C. Fungal colonies were white with sparse aerial mycelium. Acervuli containing black, slimy spore masses on the surface were present after 12 days at 25°C. Conidia were fusiform to clavate with five cells, 17.5 to 22.5 × 5.2 to 6.4 μm. Apical and basal cells were colorless, while the middle cells were heterochrome; the upper two middle cells were darker than the lower one (3). There were two or three hyaline filamentous appendages (mostly two), 14.5 to 20.6 μm long, attached to each apical cell, and one hyaline appendage (3.5 to 6.6 μm long) attached to each basal cell. Cultural and morphological characteristics of these isolates matched the genus description for Pestalotiopsis (2). The universal rDNA-ITS primer pair ITS4/ITS5 was used to amplify a DNA fragment of approximately 633 bp. The amplified PCR products were sequenced and compared through BLASTn analysis. Sequences of all isolates were identical and 99% similar to Pestalotiopsis vismiae (GenBank Accession Nos. FJ481027.1 and AB251916.1) and P. hansenii. The sequence of isolate RCEF6350 was deposited in GenBank (KM015217). Morphological features best match P. vismiae and with the supporting molecular data, the pathogen was identified as P. vismiae. To confirm pathogenicity, conidial suspensions (10 conidia ml) of each of two isolates were inoculated in three holes (0.5 cm in diameter) drilled to the cambium of each of 12 trees (15 years old). Distilled water was the control. Holes were wrapped with wet absorbent cotton and Parafilm. After 30 days, 62.5% of the inoculated trees developed symptoms similar to natural infections of P. vismiae, whereas control trees remained symptomless. P. vismiae with identical morphology was re-isolated from the lesions to complete Koch's postulates. Therefore, P. vismiae was identified as the causal agent for trunk disease of C. cathayensis in China. P. vismiae was previously reported as a pathogen of Myrica rubra (1); to our knowledge, this is the first report of P. vismiae as a pathogen on Chinese hickory in China. References: (1) F. Y. Chen et al. Plant Dis. 96:588, 2012. (2) Q. X. Ge et al. Flora Fungorum Sinicorum. Vol. 38, Pestalotiopsis. Science Press, Beijing, 2009. (3) J. X. Zhang. Master's thesis, Zhejiang University, Hangzhou, 2003.

摘要

山核桃是中国安徽和浙江的一种重要经济林木。在2010年至2013年开展的一项调查中,发现安徽省宁国市的山核桃发生了严重的树干病害。2013年,该地区近20%的山核桃果园和5%的山核桃树受到影响。5月至11月观察到的症状包括树干上出现深褐色树皮病斑和树皮开裂。树皮裂缝随着时间推移而增大(大多超过80厘米长),延伸至韧皮部,导致大面积树皮脱落,其下木质部变色。在大多数情况下,受感染植株在2至4年内死亡。从南溪镇的16个果园和胡乐镇的8个果园采集的受感染样本,用1.5%次氯酸钠进行表面消毒2分钟,接种到马铃薯葡萄糖琼脂(PDA)平板上,于25°C黑暗条件下培养1周。从患病树干上获得了11个相似的分离物。在25°C条件下,分离物在PDA上培养7天后菌落直径达7.5厘米。真菌菌落为白色,气生菌丝稀疏。在25°C条件下培养12天后,在菌落表面出现含黑色、粘性孢子团的分生孢子盘。分生孢子梭形至棒状,具5个细胞,17.5至22.5×5.2至6.4微米。顶端和基部细胞无色,中间细胞异色;上部两个中间细胞比下部一个颜色深(3)。每个顶端细胞附着有两至三根透明丝状附属物(大多为两根),长14.5至20.6微米,每个基部细胞附着有一根透明附属物(长3.5至6.6微米)。这些分离物的培养和形态特征与拟盘多毛孢属的描述相符(2)。使用通用的rDNA-ITS引物对ITS4/ITS5扩增出一条约633 bp的DNA片段。对扩增的PCR产物进行测序,并通过BLASTn分析进行比较。所有分离物的序列相同,与芒果拟盘多毛孢(GenBank登录号:FJ481027.1和AB251916.1)和汉氏拟盘多毛孢相似度为99%。分离物RCEF6350的序列已存入GenBank(KM015217)。形态特征与芒果拟盘多毛孢最为匹配,且有分子数据支持,因此将该病原菌鉴定为芒果拟盘多毛孢。为证实致病性,将两个分离物的分生孢子悬浮液(每毫升含10个分生孢子)接种到12棵15年生树木的形成层钻的三个孔(直径0.5厘米)中。以蒸馏水作为对照。孔用湿脱脂棉和保鲜膜包裹。30天后,62.5%的接种树出现了与芒果拟盘多毛孢自然感染相似的症状,而对照树无症状。从病斑上重新分离出形态相同的芒果拟盘多毛孢,从而完成了柯赫氏法则验证。因此,芒果拟盘多毛孢被确定为中国山核桃树干病害的病原菌。芒果拟盘多毛孢此前被报道为杨梅的病原菌(1);据我们所知,这是芒果拟盘多毛孢作为中国山核桃病原菌在中国的首次报道。参考文献:(1)陈福友等,《植物病害》96:588,2012。(2)葛清秀等,《中国真菌志》第38卷,拟盘多毛孢属。科学出版社,北京,2009。(3)张静霞,硕士学位论文,浙江大学,杭州,2003。

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