Díaz Arias M M, Munkvold G P, Leandro L F
Department of Plant Pathology and Microbiology, Iowa State University, Ames 50010.
Plant Dis. 2011 Oct;95(10):1316. doi: 10.1094/PDIS-04-11-0346.
Fusarium spp. are widespread soilborne pathogens that cause important soybean diseases such as damping-off, root rot, Fusarium wilt, and sudden death syndrome. At least 12 species of Fusarium, including F. proliferatum, have been associated with soybean roots, but their relative aggressiveness as root rot pathogens is not known and pathogenicity has not been established for all reported species (2). In collaboration with 12 Iowa State University extension specialists, soybean roots were arbitrarily sampled from three fields in each of 98 Iowa counties from 2007 to 2009. Ten plants were collected from each field at V2-V3 and R3-R4 growth stages (2). Typical symptoms of Fusarium root rot (2) were observed. Symptomatic and asymptomatic root pieces were superficially sterilized in 0.5% NaOCl for 2 min, rinsed three times in sterile distilled water, and placed onto a Fusarium selective medium. Fusarium colonies were transferred to carnation leaf agar (CLA) and potato dextrose agar and later identified to species based on cultural and morphological characteristics. Of 1,230 Fusarium isolates identified, 50 were recognized as F. proliferatum based on morphological characteristics (3). F. proliferatum isolates produced abundant, aerial, white mycelium and a violet-to-dark purple pigmentation characteristic of Fusarium section Liseola. On CLA, microconidia were abundant, single celled, oval, and in chains on monophialides and polyphialides (3). Species identity was confirmed for two isolates by sequencing of the elongation factor (EF1-α) gene using the ef1 and ef2 primers (1). Identities of the resulting sequences (~680 bp) were confirmed by BLAST analysis and the FUSARIUM-ID database. Analysis resulted in a 99% match for five accessions of F. proliferatum (e.g., FD01389 and FD01858). To complete Koch's postulates, four F. proliferatum isolates were tested for pathogenicity on soybean in a greenhouse. Soybean seeds of cv. AG2306 were planted in cones (150 ml) in autoclaved soil infested with each isolate; Fusarium inoculum was applied by mixing an infested cornmeal/sand mix with soil prior to planting (4). Noninoculated control plants were grown in autoclaved soil amended with a sterile cornmeal/sand mix. Soil temperature was maintained at 18 ± 1°C by placing cones in water baths. The experiment was a completely randomized design with five replicates (single plant in a cone) per isolate and was repeated three times. Root rot severity (visually scored on a percentage scale), shoot dry weight, and root dry weight were assessed at the V3 soybean growth stage. All F. proliferatum isolates tested were pathogenic. Plants inoculated with these isolates were significantly different from the control plants in root rot severity (P = 0.001) and shoot (P = 0.023) and root (P = 0.013) dry weight. Infected plants showed dark brown lesions in the root system as well as decay of the entire taproot. F. proliferatum was reisolated from symptomatic root tissue of infected plants but not from similar tissues of control plants. To our knowledge, this is the first report of F. proliferatum causing root rot on soybean in the United States. References: (1) D. M. Geiser et al. Eur. J. Plant Pathol. 110:473, 2004. (2) G. L. Hartman et al. Compendium of Soybean Diseases. 4th ed. The American Phytopathologic Society, St. Paul, MN, 1999. (3) J. F. Leslie and B. A. Summerell. The Fusarium Laboratory Manual. Blackwell Publishing, Oxford, UK, 2006. (4) G. P. Munkvold and J. K. O'Mara. Plant Dis. 86:143, 2002.
镰刀菌属是广泛存在的土传病原菌,可引发重要的大豆病害,如猝倒病、根腐病、枯萎病和猝死综合症。至少12种镰刀菌,包括轮枝镰刀菌,已被发现与大豆根系有关,但它们作为根腐病原菌的相对致病力尚不清楚,且并非所有已报道的物种都已确定其致病性(2)。2007年至2009年期间,与12位爱荷华州立大学推广专家合作,从爱荷华州98个县的每个县的三个田地中随机采集大豆根系。在V2 - V3和R3 - R4生长阶段,从每个田地采集10株植株(2)。观察到镰刀菌根腐病的典型症状(2)。有症状和无症状的根段在0.5%次氯酸钠中进行表面消毒2分钟,在无菌蒸馏水中冲洗三次,然后置于镰刀菌选择性培养基上。将镰刀菌菌落转移至香石竹叶琼脂(CLA)和马铃薯葡萄糖琼脂上,随后根据培养和形态特征鉴定到种。在鉴定出的1230株镰刀菌分离物中,有50株根据形态特征被确认为轮枝镰刀菌(3)。轮枝镰刀菌分离物产生丰富的气生白色菌丝体以及镰刀菌属里氏组特有的紫到深紫色色素。在CLA上,小型分生孢子丰富,单细胞,椭圆形,在单瓶梗和多瓶梗上呈链状(3)。使用ef1和ef2引物对两个分离物的延伸因子(EF1-α)基因进行测序,确认了物种身份(1)。通过BLAST分析和镰刀菌鉴定数据库确认了所得序列(约680 bp)的身份。分析结果显示与五个轮枝镰刀菌种(如FD01389和FD01858)的匹配度为99%。为了完成柯赫氏法则,在温室中对四株轮枝镰刀菌分离物进行了大豆致病性测试。将AG2306品种的大豆种子种植在装有各分离物侵染的高压灭菌土壤的圆锥体(150毫升)中;在种植前,通过将侵染的玉米粉/沙子混合物与土壤混合来施加镰刀菌接种物(4)。未接种的对照植株种植在添加无菌玉米粉/沙子混合物的高压灭菌土壤中。通过将圆锥体置于水浴中,将土壤温度维持在18±1°C。该实验为完全随机设计,每个分离物有五个重复(每个圆锥体单株),并重复三次。在大豆V3生长阶段评估根腐病严重程度(以百分比直观评分)、地上部干重和根部干重。所有测试的轮枝镰刀菌分离物均具有致病性。接种这些分离物的植株在根腐病严重程度(P = 0.001)以及地上部(P = 0.023)和根部(P = 0.013)干重方面与对照植株有显著差异。受感染植株的根系出现深褐色病斑,主根也出现腐烂。从受感染植株的有症状根组织中重新分离出轮枝镰刀菌,但未从对照植株的类似组织中分离出。据我们所知,这是美国关于轮枝镰刀菌引起大豆根腐病的首次报道。参考文献:(1) D. M. Geiser等人,《欧洲植物病理学报》110:473,2004年。(2) G. L. Hartman等人,《大豆病害简编》,第4版。美国植物病理学会,明尼苏达州圣保罗,1999年。(3) J.F. Leslie和B.A. Summerell,《镰刀菌实验室手册》。布莱克威尔出版社,英国牛津,2006年。(4) G.P. Munkvold和J.K. O'Mara,《植物病害》86:143,2002年。