Zhou R J, Xu H J, Fu J F, Yang F Y, Liu Z
Department of Plant Pathology, College of Plant Protection, Shenyang Agricultural University, Shenyang, Liaoning, 110866, China.
Plant Dis. 2012 Dec;96(12):1823. doi: 10.1094/PDIS-06-12-0516-PDN.
Chinese atractylodes (Atractylodes japonica Koidz.ez Kitam.) is a perennial herb in the Compositae family, and is widely distributed in China. The dried rhizomes of the plant are used in traditional Chinese medicine. During the summer of 2011, typical signs and symptoms of Sclerotinia rot were observed on Chinese atractylodes in a production field of Liaoning Province of China. Symptoms were observed in plants at the flowering stage, distributed in patches throughout the rows, and with a disease incidence of approximately 10 to 15%. The lower mature leaves of infected plants first became yellow and wilted, basal stem areas showed a black-brown rot at the same time under conditions of high humidity, and white cottony mycelium formed along the basal stem and soil surfaces. Ultimately, the basal stem and roots rotted and the plants wilted and died quickly. Black, irregular sclerotia (average 0.8 to 6.9 mm in diameter) were also observed within the pith cavity of split stems and rotted roots. The pathogen was isolated from symptomatic tissues and sclerotia, surface disinfested with 2% sodium hypochlorite, and cultured on potato dextrose agar (PDA) (1). The fungus was mesophilic, with an optimum temperature for mycelial growth in culture of about 20°C. Colonies on PDA produced masses of white aerial mycelium, with small white flocci distributed among sclerotia. After 2 weeks, sclerotia 0.5 to 4.5 mm in diameter were produced near the margin in a uniform distribution. Sclerotia were spherical, elongated, or fused to form irregular shapes and tightly attached to the agar surface by their under surface, which could be seen through the bottom of the petri dishes. DNA sequences of five replicates were obtained using the TianGen DNA secure plant kit. The internal transcribed spacer (ITS) region of rDNA was amplified with primers ITS1/ITS4 and sequenced. BLAST analysis of the 513-bp segment showed high similarity (99%) with a sequence of Sclerotinia nivalis (GenBank Accession No. AB516670). A representative sequence was deposited in GenBank (Accession No. JX294862). The fungus isolated from symptomatic tissues was identified as S. nivalis Saito on the basis of morphological and cultural characteristics (2,3) and ITS sequence analysis. Symptoms were reproduced in the greenhouse by inoculating the basal stem and roots of 15 atractylodes plants at the 7- to 10-leaf stage. Inoculum was prepared by macerating 14-day-old PDA cultures of the fungus in a blender and placing the mixture (approximately 20 g) into the potting medium of each plant. Sterile PDA was used to inoculate the five control plants. Plants were maintained in a greenhouse at 22 to 25°C and about 75% relative humidity. After 7 to 10 days, symptoms were similar to those in the fields. Lower leaves of inoculated plants became yellow and wilted, and infected plants died 2 weeks after inoculation, whereas control plants remained healthy. The pathogen was successfully recovered from symptomatic tissues, completing Koch's postulates. To our knowledge, this is the first report of Sclerotinia rot of Chinese atractylodes. Given its wide host range, S. nivalis has great potential to become an economically important plant pathogen. References: (1) W. G. Kim and W. D. Cho. Mycobiology 30:41, 2002. (2) G. Q. Li et al. Mycol. Res. 104:232, 2000. (3) I. Saito. Mycoscience 38:227, 1997.
白术(Atractylodes japonica Koidz.ez Kitam.)是菊科多年生草本植物,在中国广泛分布。该植物的干燥根茎用于传统中药。2011年夏季,在中国辽宁省的一个生产田的白术上观察到了菌核病的典型症状和体征。在开花期的植株上观察到症状,症状呈斑块状分布于整行植株中,发病率约为10%至15%。受感染植株下部成熟叶片首先变黄枯萎,在高湿度条件下,基部茎部同时出现黑褐色腐烂,白色棉絮状菌丝体沿基部茎部和土壤表面形成。最终,基部茎部和根部腐烂,植株迅速枯萎死亡。在劈开的茎和腐烂的根的髓腔中也观察到黑色、不规则的菌核(直径平均0.8至6.9毫米)。从有症状的组织和菌核中分离出病原菌,用2%次氯酸钠进行表面消毒,然后在马铃薯葡萄糖琼脂(PDA)上培养(1)。该真菌为嗜温菌,培养时菌丝体生长的最适温度约为20°C。PDA上的菌落产生大量白色气生菌丝体,在菌核间分布有小的白色絮状物。2周后,在边缘附近均匀分布产生直径0.5至4.5毫米的菌核。菌核呈球形、椭圆形或融合形成不规则形状,并通过其下表面紧密附着在琼脂表面,可透过培养皿底部看到。使用天根植物基因组DNA提取试剂盒获得五个重复样本的DNA序列。用引物ITS1/ITS4扩增rDNA的内部转录间隔区(ITS)并进行测序。对513bp片段的BLAST分析显示与雪腐核盘菌(Sclerotinia nivalis)的一个序列具有高度相似性(99%)(GenBank登录号AB516670)。一个代表性序列保存在GenBank(登录号JX294862)。根据形态和培养特征(2,3)以及ITS序列分析,从有症状组织中分离出的真菌被鉴定为雪腐核盘菌(S. nivalis Saito)。通过接种15株7至10叶期白术植株的基部茎部和根部,在温室中再现了症状。接种物通过在搅拌机中将该真菌14天龄的PDA培养物研磨制备,并将混合物(约20克)放入每株植物的盆栽基质中。用无菌PDA接种五株对照植株。植株在22至25°C、相对湿度约75%的温室中培养。7至10天后,症状与田间相似。接种植株的下部叶片变黄枯萎,接种后2周受感染植株死亡,而对照植株保持健康。病原菌从有症状的组织中成功回收,完成了柯赫氏法则。据我们所知,这是白术菌核病的首次报道。鉴于其广泛的寄主范围,雪腐核盘菌极有可能成为一种具有经济重要性的植物病原菌。参考文献:(1)W. G. Kim和W. D. Cho。《真菌学》30:41,2002。(2)G. Q. Li等人。《真菌学研究》104:232,2000。(3)I. Saito。《真菌科学》38:227,1997。