Guo M, Pan Y M, Dai Y L, Gao Z M
Department of Plant Pathology, College of Plant Protection, Anhui Agricultural University, 130 West of Changjiang Road, Hefei, 230036, P. R. China.
Plant Dis. 2013 Oct;97(10):1380. doi: 10.1094/PDIS-03-13-0246-PDN.
Peucedanum praeruptorum Dunn, a traditional Chinese medicinal herb, is an important crop in Ningguo, China. Since 2010, leaf spot symptoms were observed yearly starting in June. Blighted leaf areas on individual plants ranged from 10 to 25% in many fields, and up to 200 ha were affected each year. Symptoms consisted of small, brown, necrotic spots uniformly distributed on the 1- to 2-week-old leaves. Small tissue pieces from the edges of lesions were disinfected in 2% NaClO for 3 min, rinsed twice in distilled water, plated on potato dextrose agar (PDA), and incubated at 25°C in darkness for 4 days. Single spore isolations were obtained for six strains. When inoculated on SNA media, the six strains produced typical septate mycelium, with the young hyphae hyaline and aged ones white greyish. Setae of the strains on SNA were brown, tip acute, 2- to 3-septate, and 32.5 to 85.6 μm long. Conidiogenous cells were hyaline, cylindrical, 2- to 3-septate, 6.2 to 16.5 μm in length, and 2.8 to 4.3 μm in width. The mature conidia were slightly curved, with round apex and truncate base, 1 to 5 oil globules, and were 13.3 to 23.8 μm in length and 3.0 to 3.9 μm in width, respectively. Appressoria were solitary or in loose groups, dark brown, irregular shapes, and were 6.8 to 9.2 μm in length and 4.3 to 7.1 μm in width. PCR amplification was carried out by utilizing the universal rDNA-ITS primer pair ITS4/ITS5 (1) and the actin gene primer pair ACT-512F and ACT-783R (2). The PCR products of ITS (GenBank Accession No. KC913201) and actin gene (KC913202) from six isolates were identical, respectively, and shared 100% identity to the ITS sequence of strain CBS 167.49 of Colletotrichum spaethianum (GU227807.1) and 99% similarity to the actin gene of strain CBS 167.49 of C. spaethianum (GU227905.1), which was isolated from Hosta sieboldiana in Germany (3). Based on the above, the isolates were identified as C. spaethianum. To confirm pathogenicity, conidial suspensions (10 conidia ml) of each of the six isolates were sprayed on four leaves per plant on five 6-month-old P. praeruptorum plants. Control plants were sprayed with water. Plants were maintained at 28°C in a greenhouse with constant humidity (RH 90%) and a 12-h photoperiod of fluorescent light. Symptoms similar to the original ones started to appear after 10 days, while the control plants remained healthy. The tests were repeated three times and the fungus was recovered and identified as C. spaethianum by both morphology and molecular characterization. To our knowledge, this is the first report of C. spaethianum causing leaf spot on P. praeruptorum in China. Since the C. spaethianum infections pose a serious threat to P. praeruptorum production, this disease needs to be considered for developing effective control strategies. References: (1) I. Carbone and L. M. Kohn. Mycologia 91:553, 1999. (2) U. Damm et al. Fung. Divers. 39:45, 2009. (3) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, 1990.
前胡是一种传统的中药材,也是中国宁国的重要作物。自2010年以来,每年6月开始出现叶斑症状。许多田块中,单株植物的叶片枯萎面积在10%至25%之间,每年受影响面积达200公顷。症状表现为在1至2周龄叶片上均匀分布的小的褐色坏死斑点。从病斑边缘取小的组织块,在2%次氯酸钠中消毒3分钟,在蒸馏水中冲洗两次,接种到马铃薯葡萄糖琼脂(PDA)上,于25°C黑暗条件下培养4天。获得了六个菌株的单孢分离物。当接种在SNA培养基上时,这六个菌株产生典型的有隔菌丝体,幼嫩菌丝无色,老化菌丝灰白色。这些菌株在SNA上的刚毛褐色,顶端尖锐,有2至3个隔膜,长32.5至85.6μm。分生孢子梗无色,圆柱形,有2至3个隔膜,长6.2至16.5μm,宽2.8至4.3μm。成熟分生孢子略弯曲,顶端圆形,基部截形,有1至5个油球,长13.3至23.8μm,宽3.0至3.9μm。附着孢单个或成松散群体,深褐色,形状不规则,长6.8至9.2μm,宽4.3至7.1μm。利用通用的rDNA-ITS引物对ITS4/ITS5(1)和肌动蛋白基因引物对ACT-512F和ACT-783R(2)进行PCR扩增。六个分离物的ITS(GenBank登录号KC913201)和肌动蛋白基因(KC913202)的PCR产物分别相同,与来自德国玉簪的炭疽菌(Colletotrichum spaethianum)菌株CBS 167.49的ITS序列(GU227807.1)有100%的同一性,与炭疽菌菌株CBS 167.49的肌动蛋白基因(GU227905.1)有99%的相似性(3)。基于以上结果,这些分离物被鉴定为炭疽菌。为了确认致病性,将六个分离物的分生孢子悬浮液(每毫升含10个分生孢子)分别喷洒在五株6月龄前胡植株的每株植物的四片叶子上。对照植株喷洒水。植株在湿度恒定(相对湿度90%)、光照周期为12小时荧光的温室中保持在28°C。10天后开始出现与最初症状相似的症状,而对照植株保持健康。该试验重复三次,回收真菌并通过形态学和分子特征鉴定为炭疽菌。据我们所知,这是中国关于炭疽菌引起前胡叶斑病的首次报道。由于炭疽菌感染对前胡生产构成严重威胁,需要考虑制定有效的防治策略。参考文献:(1)I. Carbone和L. M. Kohn。《真菌学》91:553,1999。(2)U. Damm等人。《真菌多样性》39:45,2009。(3)T. J. White等人。见《PCR实验方案:方法与应用指南》第315页。学术出版社,圣地亚哥,1990。