Suppr超能文献

立枯丝核菌AG-4在阿根廷布宜诺斯艾利斯的绿萝上的首次报道

First Report of Rhizoctonia solani AG-4 on Epipremnum aureum in Buenos Aires, Argentina.

作者信息

Wright E R, Grijalba P E, Gasoni L

机构信息

Cátedra de Fitopatología, Facultad de Agronomía Universidad de Buenos Aires, Av. San Martín 4453 (1417) Capital Federal, República Argentina.

Instituto de Microbiología y Zoología Agrícola, Instituto Nacional de Tecnología Agropecuaria, C.C. 25, (1712) Castelar, Buenos Aires, República Argentina.

出版信息

Plant Dis. 2001 Jan;85(1):96. doi: 10.1094/PDIS.2001.85.1.96C.

Abstract

Root and basal stem rot, blighting, and wilting have been observed on Epipremnum aureum (Linden ex André) plants in many nurseries in and near Buenos Aires since 1997. Infected stem tissues show an intense dark brown discoloration and water soaking near the stem base that eventually leads to plant death. To determine the causal agent of the disease, small pieces of diseased tissue were surface-sterilized for 2 min in 2% sodium hypochlorite and plated on potato-dextrose agar (PDA). Whitish colonies that eventually turned brown developed in 2 to 3 days at 22 to 24°C. Irregularly shaped sclerotia were observed. Isolates typical of Rhizoctonia solani Kuhn exhibited mycelia with branches inclined in the direction of growth, constricted at the point of union with the main hyphae, with a septum in the branch near the constriction. No telemorph was observed. Nuclei in living hyphal mats were stained directly on a microscope slide coated with water agar according to the method of Tu and Kimbrough (4) and were examined at 400× magnification. The cells were multinucleate. Anastomosis group was determined by using known tester isolates of Rhizoctonia spp. (3). Positive anastomosis was observed with tester strains of AG-4 HG-II. The polymerase chain reaction was performed according to the protocol of Boysen et al (1) in order to confirm the anastomosis group. Primers used for the amplification of the ITS region were ITSI and LROR. Amplification of the ITS region indicated lack of variation with AG-4 tester strain. The pathogenicity of the isolate was determined with the inoculum-layer technique (2), consisting of a 7-day-old petri plate culture of the pathogen in PDA that is removed from the dish and placed intact on the soil, 2 to 4 cm under the roots of 10 healthy plants. Some leaves of the plants were placed in contact with the inoculated substratum. For a control, PDA was placed under the roots of other plants. Plants were maintained at 22 to 24°C, with close-to-saturation humidity. After 6 to 10 days, symptoms were similar to those previously observed. Initially leaves that had been placed in contact with the substratum showed dark areas with a watersoaked area 2 to 3 cm in diameter. These lesions expanded over the entire leaf blade moving into the petioles and stems killing the plant. One hundred percent of inoculated plants were infected. Koch's postulates were satisfied after reisolating the fungus. The characteristics of the causal agent are those of multinucleate isolates of R. solani belonging to the anastomosis group AG-4 HG-II (3). This is the first report of R. solani causing disease on E. aureum in Argentina. References: (1) M. Boysen, M. Borja, C. Del Corral, O. Salazar, and V. Rubio. Curr. Genet. 29:174-181, 1996. (2) A. F. Schmitthenner and J. W. Hilty. Phytopathology 52:177-178, 1962. (3) B. Sneh, L. Burpee, and A. Ogoshi. 1991. Identification of Rhizoctonia Species. The American Phytopathological Society, St. Paul, MN. (4) C. C. Tu and J. W. Kimbrough. Mycologia 65:941-944, 1973.

摘要

自1997年以来,在布宜诺斯艾利斯及其附近的许多苗圃中,人们观察到绿萝(麒麟叶属(Linden ex André))植株出现根和基部茎腐病、枯萎病以及萎蔫病。受感染的茎组织在茎基部附近呈现出强烈的深褐色变色和水渍状,最终导致植株死亡。为了确定该病的病原体,将小块患病组织在2%次氯酸钠中进行2分钟的表面消毒,然后接种到马铃薯葡萄糖琼脂(PDA)上。在22至24°C条件下,2至3天内形成了最终变为褐色的白色菌落。观察到了形状不规则的菌核。立枯丝核菌(Rhizoctonia solani Kuhn)的典型分离物表现出菌丝,其分支朝着生长方向倾斜,在与主菌丝结合点处缢缩,在缢缩附近的分支中有一个隔膜。未观察到有性态。根据Tu和Kimbrough(4)的方法,将活菌丝体上的细胞核直接在涂有水琼脂的显微镜载玻片上染色,并在400倍放大倍数下进行检查。细胞为多核。通过使用立枯丝核菌属(Rhizoctonia spp.)已知的测试分离物(3)来确定融合群。观察到与AG-4 HG-II测试菌株有阳性融合。按照Boysen等人(1)的方案进行聚合酶链反应,以确认融合群。用于扩增ITS区域的引物是ITSI和LROR。ITS区域的扩增表明与AG-4测试菌株没有差异。通过接种层技术(2)确定分离物的致病性,该技术包括将在PDA中培养7天的病原菌平板培养物从培养皿中取出,完整地放置在土壤中,在10株健康植株根部下方2至4厘米处。使植株的一些叶子与接种的基质接触。作为对照,将PDA放置在其他植株的根部下方。植株保持在22至24°C,湿度接近饱和。6至10天后,症状与之前观察到的相似。最初与基质接触的叶子出现深色区域,有直径2至3厘米的水渍状区域。这些病斑扩展到整个叶片,蔓延到叶柄和茎部,导致植株死亡。100%的接种植株被感染。重新分离出真菌后,科赫法则得到满足。病原体的特征是属于融合群AG-4 HG-II的立枯丝核菌多核分离物的特征(3)。这是阿根廷关于立枯丝核菌引起绿萝病害的首次报道。参考文献:(1)M. Boysen、M. Borja、C. Del Corral、O. Salazar和V. Rubio。《当代遗传学》29:174 - 181,1996年。(2)A. F. Schmitthenner和J. W. Hilty。《植物病理学》52:177 - 178,1962年。(3)B. Sneh、L. Burpee和A. Ogoshi。1991年。《立枯丝核菌物种的鉴定》。美国植物病理学会,明尼苏达州圣保罗。(4)C. C. Tu和J. W. Kimbrough。《真菌学》65:941 - 944,1973年。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验