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林业科学 ›› 2015, Vol. 51 ›› Issue (10): 142-147.doi: 10.11707/j.1001-7488.20151018

• 研究简报 • 上一篇    下一篇

美国红枫褐斑病病原菌鉴定

崔朝宇1, 王园秀1,2, 蒋军喜1, 欧阳慧1, 秦双林1, 黄婷1   

  1. 1. 江西农业大学农学院 南昌 330045;
    2. 江西农业大学生物科学与工程学院 南昌 330045
  • 收稿日期:2014-07-08 修回日期:2014-08-22 出版日期:2015-10-25 发布日期:2015-11-10
  • 通讯作者: 蒋军喜
  • 基金资助:
    国家自然科学基金项目(31160358)。

Identification of the Pathogen Causing Brown Spot Disease of Acer rubrum ‘October Glory’

Cui Chaoyu1, Wang Yuanxiu1,2, Jiang Junxi1, Ouyang Hui1, Qin Shuanglin1, Huang Ting1   

  1. 1. College of Agronomy, Jiangxi Agricultural University Nanchang 330045;
    2. College of Bioscience and Bioengineering, Jiangxi Agricultural University Nanchang 330045
  • Received:2014-07-08 Revised:2014-08-22 Online:2015-10-25 Published:2015-11-10

摘要: [目的] 鉴定江西省鄱阳县美国红枫褐斑病的病原,为该病害的防治和进一步研究奠定基础。[方法] 实地调查该病害的发生时期和为害程度,对病害症状进行观察记载。随机采集30份不同发病阶段的病叶样品,采用PDA培养基按照常规组织分离法对其进行病菌分离和菌种纯化。选择代表性菌株PM-1和PM-2作为供试菌株,用浓度为1×106个·mL-1的孢子悬浮液对美国红枫健康叶片进行刺伤接种,并对接种发病后病斑进行病菌再分离,以完成柯赫氏法则验证。将各分离菌株接种于PDA平板中央,于25 ℃黑暗条件下培养,逐日观察测量菌落大小、颜色、形状、质地及产孢情况等性状。对自然发病寄主上着生的病菌和人工培养的病菌分别制作切片,在显微镜下观察载孢体及分生孢子形态,并测量其大小。根据培养菌落形态特征和病菌形态大小,参考相关文献,对病原菌进行种类归属鉴定。提取病菌基因组DNA,采用真核生物核糖体基因转录间隔区(ITS)通用引物ITS1(5'-TCCGTAGGTGAACCTGCGG-3')和ITS4(5'-TCCTCCGCTTATTGATATGC-3')对病菌ITS-5.8S rDNA区段进行PCR扩增和序列测定。使用BLAST工具软件,在GenBank中进行序列同源性搜索,并利用MegA 5.2软件中的邻位加入法构建系统发育树,以对病菌进行分子鉴定。[结果] 美国红枫褐斑病只为害叶片,5月中旬始发,6月中下旬进入盛发期,重病株发病率达60%以上。病斑常呈圆形、椭圆形或不规则形,中央黄褐色,边缘黑褐色,周围有黄色晕圈,后期病斑常联合成大斑,造成叶片大面积枯死而脱落。在潮湿条件下,在病斑上常形成黑色小点,为病菌的分生孢子盘和分生孢子。共分离获得25个培养性状一致的真菌菌株,菌落正面白色,绒状,平铺,背面淡黄色。分离菌株具有致病性,人工接种发病症状与自然发病症状相同。病菌载孢体为分生孢子盘,直径108~205 μm; 分生孢子纺锤形,直或微弯,5个细胞,大小(19.3~26.8) μm×(5.3~6.8) μm; 中间3个细胞褐色,长11.9~17.0 μm; 顶细胞长圆锥形,顶生2~4根不分枝的附属丝,无色透明,长6.3~18.3 μm; 基细胞无色,具短柄,长1.8~7.5 μm。病菌ITS-rDNA序列长606 nt,与GenBank中小孢拟盘多毛孢的序列同源性为100%,在系统发育树上,与小孢拟盘多毛孢的亲缘关系也最近。[结论] 形态学和分子生物学鉴定结果表明,引起江西省鄱阳县美国红枫褐斑病的病原菌为小孢拟盘多毛孢,属于子囊菌无性型拟盘多毛孢属真菌。

关键词: 美国红枫, 褐斑病, 病原菌鉴定, 小孢拟盘多毛孢

Abstract: [Objective] A newly found brown spot disease widely infests leaves of Acer rubrum 'October Glory' growing in Poyang, Jiangxi, and the pathogen is unknown.In this study the pathogen was identified for the purpose of controlling and futher studying the disease. [Method] Occurrence period and incidence rate of the disease were investigated on the spot, and symptoms of the disease were observed and described. A total of 30 infested leaf samples at different developing stages were randomly collected. Pathogen isolation and purification from the samples were conducted on PDA medium using normal tissue isolation method. In order to fulfil Koch'postulates, pathogenicity test was done by artificially inoculating healthy leaves of A.rubrum 'October Glory' with spore suspension (1×106·mL-1) of two representative isolates PM-1 and PM-2 respectively, and then the pathogen was re-isolated from the newly produced lesions. The tested isolates were inoculated on the center of PDA plates and incubated in 25 ℃ and darkness conditions for their growth, and the colony characteristics of size, color, shape and texture were daily observed. Slice samples as to pathogen on naturally infected plants as well as on PDA plates were prepared respectively, and they were microscopically observed and measured to get the morphology and size of conidiomata and conidia of the pathogen. The pathogen species was identified based on comparing its cultural and morphological results with corresponding description in related literature. DNA of the pathogen was extracted and used as template to amplify the ITS-5.8S rDNA region by PCR with primer pair ITS1/ITS4, and the PCR products were directly sequenced. For pathogenic identification on molecular level, nucleotide sequence homology was searched in GenBank using BLAST software, and phylogenetic tree was constructed by the neighbor-joining method. [Result] The brown spot disease of A. rubrum 'October Glory' occurred only on the leaves. It initially appeared in mid-May, and its peak period was in mid-late June with more than 60% incidence of disease. The lesions were circular, oval or irregular, and yellow-brown with black-brown borders which were often surrounded by a yellowish halo. Later, several lesions might coalesce, and severely affected leaves were withered and fell off. Under humid conditions, black spots, i.e. the acervuli and conidia were produced on the lesions. Totally 25 fungal isolates with the same cultural characteristics were obtained, and their colonies were all fluffy, flat and white on front side and light yellow on back side. Pathogenicity test indicated that PM-1 and PM-2 produced the same symptoms as the naturally infected ones. The spore-bearing structures, acervuli, were 108~ 205 μm in diameter. They produced fusiform, straight to slightly curved conidia with size of (19.3-26.8)μm×(5.3-6.8)μm. Each conidium contained 5 cells with three median cells dark brown and 11.9~17.0 μm long. Apical cell was hyaline, conico-acuminate, 6.3~18.3 μm long, with 2-4 non-branched, colorless and transparent appendages. The basal cell was also hyaline and had a short handle with 1.8~7.5 μm in length. ITS-5.8S rDNA sequence of the pathogen was 606 nucleotide long,which shared 100% homology with Pestalotiopsis microspore in GenBank, and had the closest relationship with the fungus in the phylogenetic tree.[Conclusion] Based on morphological and molecular identification results, it is considered that the pathogen causing brown spot disease of Acer rubrum 'October Glory' in Poyang, Jiangxi is Pestalotiopsis microspora (Speg.) G.C. Zhao & N. Li,a fungal species which belonged to genus pestalotiopsis, a anamorph in Ascomycota. This is the first report of Pestalotiopsis microspore paratisizing on Acer rubrum 'October Glory' and causing brown spot disease.

Key words: Acer rubrum, brown spot disease, pathogen identification, Pestalotiopsis microspora

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