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中国甜菜幼苗立枯病由双核丝核菌AG-A引起的首次报道

First Report of Sugar Beet Seedling Damping-Off Caused by Binucleate Rhizoctonia AG-A in China.

作者信息

Wang P P, Wu X H

机构信息

Department of Plant Pathology, China Agricultural University, Beijing 100193, China.

出版信息

Plant Dis. 2012 Nov;96(11):1696. doi: 10.1094/PDIS-05-12-0492-PDN.

DOI:10.1094/PDIS-05-12-0492-PDN
PMID:30727498
Abstract

Sugar beet (Beta vulgaris L.) is grown worldwide and produces one-third of the world's sugar supply. Sugar beet seedling Rhizoctonia damping-off is an important disease mainly caused by Rhizoctonia solani AG-2, AG-4, and AG-5 (2). In 2010, diseased sugar beet seedlings with about 20% incidence affected by damping-off, which showed dark brown lesions on the stems just below the soil surface and portions of the roots, were collected from nurseries in three locations in Heilongjiang province, northeast China. Root fragments taken from the margins of healthy tissues and lesions on roots were surface disinfected with 0.5% sodium hypochlorite for 2 min, rinsed with sterile water, then placed on potato dextrose agar (PDA) and incubated at 25°C in the dark. Three (designed HLJ-RAA1, HLJ-RAB1, HLJ-RAB2) of nine Rhizoctonia isolates were obtained from diseased tissues and preliminarily identified as binucleate Rhizoctonia (BNR) anamorph (teleomorph Ceratobasidium Rogers) species-like. Fungal colonies were white with large amounts of floccose, aerial hyphae. Hyphal cells were determined to be binucleate when stained with 4'-6-diamidino-2-phenylindole (DAPI) (1). No sclerotia were produced after 14 days on PDA. Average hyphal diameter of the three isolates were 4.2, 4.3, and 4.8 μm, respectively. Further, the internal transcribed spacer (ITS) region of rDNA was amplified from the genomic DNA extracted from hyphae by bead beating in 2% CTAB solution using stainless steel beads with primers ITS1 and ITS4. The ITS sequences (GenBank Accession Nos. JX073668, JX073669, and JX073670) were over 99% identical to those of more than 50 Ceratobasidium sp. AG-A isolates (e.g., GenBank Accession No. JQ688054.1; strain HY-15). Therefore, based on morphological and molecular characteristics, these isolates were identified to be BNR AG-A. To determine the pathogenicity of the isolates, sugar beet (cv. HI0305) seedlings were inoculated with wheat seeds colonized with each of the isolated Rhizoctonia strains (one seed per seedling), and grew in pots under greenhouse conditions (3). After 3 weeks, some inoculated plants showed damping-off as observed in the nurseries, whereas noninoculated control plants (sterile wheat seeds only) remained healthy. Disease incidence from the trials averaged 53.3%, 70%, and 53.3% for the isolates HLJ-RAA1, HLJ-RAB1, and HLJ-RAB2, respectively. The three BNR cultures of the pathogens were consistently reisolated from symptomatic roots, and their identities confirmed by morphological and molecular characteristics as described above, fulfilling Koch's postulates. BNR AG-A was previously reported to be pathogenic to soybean, pea, snap bean, and pak choy in China (4). However, to our knowledge, this is the first report of BNR AG-A causing sugar beet seedling damping-off in China. Sugar beet is often grown in crop rotation with soya bean and such a rotation could increase the risk of soilborne infection to either crop by BNR AG-A. References: (1) W. C. Kronland and M. E. Stanghellini. Phytopathology 78:820, 1988. (2) E. O'Sullivan and J. A. Kavanagh. Plant Pathol. 40:128, 1991. (3) C. E. Windels and D. J. Nabben. Phytopathology 79:83, 1989. (4) G. H. Yang et al. J. Phytopathol. 153:333, 2005.

摘要

甜菜(Beta vulgaris L.)在全球范围内种植,其产量占全球食糖供应量的三分之一。甜菜幼苗立枯丝核菌猝倒病是一种重要病害,主要由立枯丝核菌AG - 2、AG - 4和AG - 5引起(2)。2010年,从中国东北黑龙江省三个地点的苗圃中采集了发病率约为20%的受猝倒病影响的甜菜病苗,这些病苗在土壤表面以下的茎部和部分根部出现深褐色病斑。从病根健康组织边缘和病斑处取根段,用0.5%次氯酸钠进行表面消毒2分钟,用无菌水冲洗,然后置于马铃薯葡萄糖琼脂(PDA)上,在25°C黑暗条件下培养。从病组织中获得了9个丝核菌分离株中的3个(分别命名为HLJ - RAA1、HLJ - RAB1、HLJ - RAB2),初步鉴定为双核丝核菌(BNR)无性型(有性型为角担菌属罗杰斯种)类似种。真菌菌落白色,有大量絮状气生菌丝。用4′,6 - 二脒基 - 2 - 苯基吲哚(DAPI)染色后,菌丝细胞被确定为双核(1)。在PDA上培养14天后未产生菌核。这三个分离株的平均菌丝直径分别为4.2、4.3和4.8μm。此外,使用引物ITS1和ITS4,通过在2% CTAB溶液中用不锈钢珠研磨从菌丝中提取的基因组DNA,扩增rDNA的内部转录间隔区(ITS)。ITS序列(GenBank登录号JX073668、JX073669和JX073670)与50多个角担菌属AG - A分离株(如GenBank登录号JQ688054.1;菌株HY - 15)的序列相似度超过99%。因此,根据形态和分子特征,这些分离株被鉴定为BNR AG - A。为了确定分离株的致病性,用接种了各分离丝核菌菌株的小麦种子(每株幼苗一粒种子)接种甜菜(品种HI0305)幼苗,并在温室条件下盆栽生长(3)。3周后,一些接种的植株出现了如苗圃中观察到的猝倒现象,而未接种的对照植株(仅无菌小麦种子)保持健康。分离株HLJ - RAA1、HLJ - RAB1和HLJ - RAB2的试验发病率分别平均为53.3%、70%和53.3%。从有症状的根部持续重新分离出病原菌的这三种BNR培养物,并通过上述形态和分子特征确认其身份,满足科赫法则。此前在中国报道BNR AG - A对大豆、豌豆、菜豆和小白菜致病(4)。然而,据我们所知,这是中国关于BNR AG - A引起甜菜幼苗猝倒病的首次报道。甜菜常与大豆轮作,这样的轮作可能会增加BNR AG - A对两种作物土传感染的风险。参考文献:(1)W. C. Kronland和M. E. Stanghellini。植物病理学78:820,1988。(2)E. O'Sullivan和J. A. Kavanagh。植物病理学40:128,1991。(3)C. E. Windels和D. J. Nabben。植物病理学79:83,1989。(4)G. H. Yang等。植物病理学杂志153:333,2005。

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