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棕榈疫霉引起中国木薯根腐病的首次报道

First Report of Phytophthora palmivora Causing Root Rot of Cassava in China.

作者信息

Guo H, Li C-P, Shi T, Fan C-J, Huang G-X

机构信息

Environment and Plant Protection Institute, CATAS, Key Laboratory of Integrated Pest Management on Tropical Crops, Ministry of Agriculture, Hainan Key Laboratory for Monitoring and Control of Tropical Agricultural Pests, Danzhou, Hainan 571737, P. R. China. This work was partly supported by the fund for Modern Agro-Industry Technology Research System (CARS-12-hnhgx) from the Ministry of Agriculture, the People's Republic of China.

出版信息

Plant Dis. 2012 Jul;96(7):1072. doi: 10.1094/PDIS-09-11-0780-PDN.

Abstract

Cassava (Manihot esculenta) is an economically important crop grown widely in South China. Seventy percent of the cassava grown is used for starch and ethanol production and it has become the foundation of local food and bioenergy systems. In November 2010, a new root rot disease was found on cv. HuaNan205 from a cassava plantation in Danzhou, Hainan Province. Disease occurred on 30% or less of the plants. Initially, the upper leaves wilted at noon and recovered in the evening. Eventually, infected plants no longer recovered and the whole plant wilted and died. Root rot symptoms consisting of irregular brown patches occurred on the tuberous roots. Symptomatic root rot tissue was cut into 1-cm pieces, washed in distilled water, and soaked in a solution of 1% sodium hypochlorite for 3 min. A subsection was cut from each sterilized piece, placed on a plate of V8 agar medium, and incubated at 28°C for 7 days. Pathogenicity was established by following Koch's postulates. In July 2011, 10 plants of cassava cv. HuaNan205 were selected from a disease-free plantation in Danzhou. The pathogen was cultivated on V8 agar at 28°C for 14 days. Four holes were established 15 cm from the base of the cassava plants. Five plants were inoculated with 100 mL of the mycelial suspension in each of the four spots and covered by soil. The other five plants were treated with sterile water as control. Plants were maintained for 4 months. All five of the inoculated plants wilted and two died, while the control plants grew normally. Symptoms similar to the original root lesions were observed on tuberous roots of inoculated plants, while only scars formed on tuberous roots of control plants. The pathogen was reisolated from the lesions of inoculated plants. Microscopic examination showed the sporangia as papillate and ovoid with the widest part close to the base. They were easily washed off and each detached sporangium contained a short pedicel 1.2 to 6.9 μm long, average 2.9 μm. Chlamydospores were readily observed on diseased roots and observed in pure cultures on V8 agar. Morphological characteristics of the specimen were similar to the descriptions for Phytophthora palmivora (2). Genomic DNA of this isolate was extracted with a cetyltrimethylammoniumbromide protocol (3) from mycelium and used as a template for amplification of the internal transcribed spacer (ITS) region of rDNA with primer pair ITS1/ITS4 (1). The sequence (GenBank Accession No. HE580279) exactly matched several sequences (e.g., GenBank Accession Nos. HQ237481.1, AY745750, and AY745751) of P. palmivora. To our knowledge, this is the first report of root rot caused by P. palmivora on cassava in China. References: (1) D. E. L. Cooke et al. Fungal Genet. Biol. 30:17, 2000. (2) D. C. Erwin and O. K. Ribeiro. Phytophthora Diseases Worldwide. The American Phytopathological Society, St. Paul, MN, 1996. (3) J. R. Xu et al. Genetics 143:175, 1996.

摘要

木薯(Manihot esculenta)是一种经济上重要的作物,在中国南方广泛种植。所种植木薯的70%用于淀粉和乙醇生产,它已成为当地食品和生物能源系统的基础。2010年11月,在海南省儋州市一个木薯种植园中,华南205品种上发现了一种新的根腐病。发病植株占比30%或更低。最初,上部叶片在中午萎蔫,傍晚恢复。最终,受感染植株不再恢复,整株萎蔫死亡。块根上出现了由不规则褐色斑块组成的根腐症状。将有症状的根腐组织切成1厘米长的小段,用蒸馏水冲洗,然后浸泡在1%次氯酸钠溶液中3分钟。从每个消毒后的小段上切下一小部分,放在V8琼脂培养基平板上,在28°C下培养7天。按照科赫法则确定致病性。2011年7月,从儋州市一个无病种植园中选取10株木薯华南205品种。将病原菌在V8琼脂上于28°C培养14天。在距木薯植株基部15厘米处打四个孔。在四个点中的每一个点,给五株植株接种100毫升菌丝悬浮液,并用土壤覆盖。另外五株植株用无菌水处理作为对照。植株养护4个月。所有五株接种植株都萎蔫了,两株死亡,而对照植株正常生长。在接种植株的块根上观察到了与最初根病变相似的症状,而对照植株的块根上只形成了疤痕。从接种植株的病变部位重新分离出病原菌。显微镜检查显示孢子囊为乳头状和卵形,最宽处靠近基部。它们很容易脱落,每个分离的孢子囊含有一个1.2至6.9微米长、平均2.9微米的短梗。在患病根上很容易观察到厚垣孢子,在V8琼脂上的纯培养物中也能观察到。该标本的形态特征与棕榈疫霉(Phytophthora palmivora)的描述相似(2)。用十六烷基三甲基溴化铵法(3)从菌丝体中提取该分离株的基因组DNA,并用作引物对ITS1/ITS4(1)扩增rDNA内部转录间隔区(ITS)的模板。该序列(GenBank登录号HE580279)与棕榈疫霉的几个序列(如GenBank登录号HQ237481.1、AY745750和AY745751)完全匹配。据我们所知,这是中国关于棕榈疫霉引起木薯根腐病的首次报道。参考文献:(1)D. E. L. Cooke等人,《真菌遗传学与生物学》30:17,2000年。(2)D. C. Erwin和O. K. Ribeiro,《全球疫霉病》,美国植物病理学会,明尼苏达州圣保罗,1996年。(3)J. R. Xu等人,《遗传学》143:175,1996年。

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