Luan Y S, Shang Z T, Su Q, Feng L, An L J
Department of Bioscience and Bioengineering, Dalian University of Technology, Dalian, 116023, China.
Institute of Applied Ecology, Chinese Academy of Science, Shenyang, 110016, China.
Plant Dis. 2008 Jan;92(1):171. doi: 10.1094/PDIS-92-1-0171A.
In August 2006, leaf spots were observed on half-high blueberry (Vaccinium corymbosum) in a plant nursery in Dalian, China. The symptomatic potted 1-year-old blueberry plants were located in parts of a plant nursery with poor ventilation. The primary symptom was a leaf spot, 0.4 to 0.8 cm in diameter, with brown margins that enlarged and coalesced. Mycelium grew from symptomatic and green leaf tissue removed from the margin of a necrotic leaf spot. Plant tissues were surface disinfested with 0.1% mercuric chloride for 3 min and 70% ethyl alcohol for 30 s before plating onto potato dextrose agar. The resulting colonies were white with a regular margin and a rough surface. The cultures were covered with black and globular acervuli with a diameter of 100 to 200 μm. The base of each conidiophore was swollen and globose with phialides growing from the apical end. Mature conidia were straight to fusiform, measuring 19.0 to 27.5 × 6.3 to 9.2 μm, and five-celled with the three middle cells brown and darker than the end cells. The apical cell was triangular and hyaline with three simple setulae that were 17.2 to 29.7 μm long. The base cell terminated in a point 4.0 to 8.6 μm long. Koch's postulates were fulfilled for the fungus by spray inoculating two healthy young plants with 2 × 10 conidia per ml of sterile distilled water. As a control, two similar plants were sprayed with sterile water. Plants were placed inside plastic bags to maintain humidity and incubated in a growth chamber at 26°C under fluorescent light for 14 h and at 20°C in darkness for 10 h. After 3 days, the plastic bags were removed and plants were maintained under the same conditions. More than 20 days after inoculation, symptoms on inoculated plants were similar to those previously described in the nursery. Control plants did not show any symptoms. Cultures isolated from the lesions were similar to those isolated previously from plants in the nursery. The morphological descriptions and measurements were similar to Pestalotiopsis clavispora (1). The 5.8S subunit and flanking internal transcribed spacers (ITS1 and ITS2) of rDNA and partial β-tubulin gene were amplified from DNA extracted from single-spore cultures using the ITS1/ITS4 and T1/Bt2b primers (2) respectively, and sequenced (GenBank Accession Nos. EF119336 and EF152585). The ITS sequences were most similar to the ITS regions of P. clavispora TA-8 (98%; GenBank Accession No. AY924264), P. clavispora TA-6 (98%; GenBank Accession No. AY924263), and P. clavispora PSHI 2002 Endo 389 (96%; GenBank Accession No. AY682929). The partial β-tubulin gene sequence was identical to Pestalotiopsis sp. isolate PSHI 2004 Endo 86 (100%; GenBank Accession No. DQ657901). The morphology and sequence data support the identity of the causal fungus as P. clavispora. To our knowledge, this is the first report on the presence of a Pestalotiopsis sp. causing a disease of blueberry in China. References: (1) E. F. Guba. Monograph of Monochaetia and Pestalotia. Harvard University Press, Cambridge, MA, 1961. (2) W. Tao et al. Mol. Cell Biol. 27:689, 2007.
2006年8月,在中国大连的一家植物苗圃中,半高蓝莓(Vaccinium corymbosum)上发现了叶斑病。有症状的1年生盆栽蓝莓植株位于苗圃中通风不良的区域。主要症状是叶斑,直径0.4至0.8厘米,边缘褐色,病斑会扩大并融合。从坏死叶斑边缘取下的有症状和绿色叶片组织上长出了菌丝体。在接种到马铃薯葡萄糖琼脂平板之前,植物组织先用0.1%的氯化汞进行表面消毒3分钟,再用70%的乙醇消毒30秒。产生的菌落为白色,边缘规则,表面粗糙。培养物上覆盖着直径为100至200μm的黑色球状分生孢子盘。每个分生孢子梗基部肿胀呈球形,顶端有瓶梗。成熟的分生孢子直或呈梭形,大小为19.0至27.5×6.3至9.2μm,五细胞,中间三个细胞褐色,比两端细胞颜色深。顶端细胞呈三角形,透明,有三根长17.2至29.7μm的简单刚毛。基部细胞末端呈一个长4.0至8.6μm的尖。通过用每毫升无菌蒸馏水含2×10个分生孢子的菌悬液喷雾接种两株健康的年轻植株,该真菌满足了柯赫氏法则。作为对照,对两株相似的植株喷洒无菌水。将植株置于塑料袋内以保持湿度,并在生长室中于26°C的荧光灯下培养14小时,在20°C的黑暗中培养10小时。3天后,取下塑料袋,植株在相同条件下继续培养。接种20多天后,接种植株上的症状与苗圃中先前描述的症状相似。对照植株未表现出任何症状。从病斑分离得到的培养物与先前从苗圃植株分离得到的培养物相似。形态学描述和测量结果与棒形拟盘多毛孢(Pestalotiopsis clavispora)相符(1)。使用ITS1/ITS4和T1/Bt2b引物(2)分别从单孢培养物提取的DNA中扩增出rDNA的5.8S亚基及其侧翼的内部转录间隔区(ITS1和ITS2)和部分β-微管蛋白基因,并进行测序(GenBank登录号分别为EF119336和EF152585)。ITS序列与棒形拟盘多毛孢TA - 8(98%;GenBank登录号AY924264)、棒形拟盘多毛孢TA - 6(98%;GenBank登录号AY924263)和棒形拟盘多毛孢PSHI 2002 Endo 389(96%;GenBank登录号AY682929)的ITS区域最相似。部分β-微管蛋白基因序列与拟盘多毛孢属菌株PSHI 2004 Endo 86(100%;GenBank登录号DQ657901)完全相同。形态学和序列数据支持致病真菌为棒形拟盘多毛孢的鉴定。据我们所知,这是中国首次报道有拟盘多毛孢属真菌引起蓝莓病害。参考文献:(1)E. F. Guba. Monograph of Monochaetia and Pestalotia. Harvard University Press, Cambridge, MA, 1961. (2)W. Tao等. Mol. Cell Biol. 27:689, 2007.