Chen C H, Wang T C, Seo M J
AVRDC-The World Vegetable Center, P.O. Box 42, Shanhua, Tainan 74199, Taiwan.
National Institute of Crop Science, RDA, 209 Seodum-Dong, Suwon, Republic of Korea, 441-857.
Plant Dis. 2009 Feb;93(2):202. doi: 10.1094/PDIS-93-2-0202A.
Genera, Diaporthe and Phomopsis, from an important pathogenic complex of soybean (Glycine max) throughout the world, cause reductions in plant stands, yield, and seed health and quality (1). In a study of the Diaporthe/Phomopsis complex in Taiwan in March 2008, four stem samples with black fruiting structures in linear rows on senescent soybean were collected from the research fields at AVRDC, Shanhua, Tainan, Taiwan. Unidentified fungal isolates were obtained by surface disinfection of infected stems and plating excised tissues on potato dextrose agar (PDA). Colonies of the isolates showed ropelike white mycelia with yellowish tonalities. Small and scattered black stromata were observed frequently in the medium. Mutic pycnidia were found solitarily or aggregated in conidiomata on PDA plates after 10 days of incubation at 24°C with a 12-h photoperiod with near-UV light. All isolates produced α-conidia that measured 8.78 × 3.32 (7.00 to11.00 × 3.00 to 4.00) μm, and sporadically, β-conidia of 30.58 × 0.85 (26.00 to 33.00 × 0.60 to 1.20) μm. Perithecia were not observed in the collected stem samples or the fungal cultures on PDA. Restriction fragment length polymorphism patterns of the PCR products amplified by ITS and ITS primers for all isolates were identical to the patterns reported for Diaporthe phaseolorum var. sojae (3). Thus, all isolates were identified as D. phaseolorum var. sojae on the basis of morphologic and genetic characteristics (2,3). Pathogenicity was confirmed through inoculations during the V2 growth stage of soybean seedlings by atomizing conidial suspensions (1 × 10 α-conidia/ml) of each isolate on soybean seedlings as well as by injecting the inoculum into soybean stems separately. Four plants in each of three replications were inoculated for each method and six noninoculated plants served as controls. Plants were incubated in a growth chamber at 25°C and maintaining relative humidity at 100% by a humidifier for 48 h in darkness; thereafter, plants were maintained in the greenhouse at temperatures ranging from 23 to 34°C. Seven days after inoculation, red-brown leaf spots and coalescent lesions were observed on seedlings atomized by inoculum suspensions, as well as brown lesions and black pycnida in linear rows observed on plants inoculated by stem injection. No symptoms were observed on noninoculated plants. The fungal isolates obtained from inoculated soybeans were morphologically identical to those used as inoculum. The pathogenicity test was repeated twice. To our knowledge, this is the first explicit report identifying the causal agent of soybean pod and stem blight in Taiwan. The vouchers of infected specimens are available at AVRDC-The World Vegetable Center. Reference: (1) R. P. Mulrooney. Plant Dis. 70:600, 1988. (2) R. N. Pioli et al. Phytopathology 93:136, 2003. (3) A. W. Zhang et al. Phytopathology 88:1306, 1998.
间座壳属(Diaporthe)和拟茎点霉属(Phomopsis)是全球大豆(Glycine max)重要致病复合体的组成部分,会导致大豆植株数量减少、产量降低以及种子健康和品质下降(1)。2008年3月在台湾对间座壳属/拟茎点霉属复合体进行的一项研究中,从台湾台南善化亚洲蔬菜研究与发展中心(AVRDC)的试验田中,采集了4个在衰老大豆上带有呈线性排列黑色子实体结构的茎样本。通过对受感染的茎进行表面消毒,并将切下的组织接种在马铃薯葡萄糖琼脂(PDA)上,获得了未鉴定的真菌分离株。分离株的菌落呈现出绳状白色菌丝体,带有淡黄色调。在培养基中经常观察到小而分散的黑色子座。在24°C、12小时光周期和近紫外光条件下培养10天后,在PDA平板上发现分生孢子器单个或聚集在分生孢子盘内,有多个分生孢子器。所有分离株均产生α分生孢子,大小为8.78 × 3.32(7.00至11.00 × 3.00至4.00)μm,偶尔还产生大小为30.58 × 0.85(26.00至33.00 × 0.60至1.20)μm的β分生孢子。在所采集的茎样本或PDA上的真菌培养物中均未观察到子囊壳。所有分离株经ITS和ITS引物扩增的PCR产物的限制性片段长度多态性模式,与报道的菜豆间座壳大豆变种(Diaporthe phaseolorum var. sojae)的模式相同(3)。因此,根据形态学和遗传学特征,所有分离株均被鉴定为菜豆间座壳大豆变种(2,3)。通过在大豆幼苗V2生长阶段进行接种来确认致病性,方法是将每个分离株的分生孢子悬浮液(1×10α分生孢子/ml)雾化到大豆幼苗上,以及分别将接种物注射到大豆茎中。每种方法接种三个重复,每个重复4株植物,6株未接种的植物作为对照。将植物置于生长室中,在25°C下,用加湿器保持相对湿度100%,黑暗处理48小时;此后,将植物置于温度为23至34°C的温室中。接种7天后,在接种物悬浮液雾化处理的幼苗上观察到红棕色叶斑和融合性病斑,在茎注射接种的植物上观察到褐色病斑和呈线性排列的黑色分生孢子器。未接种的植物未观察到症状。从接种大豆中获得的真菌分离株在形态上与用作接种物的分离株相同。致病性试验重复了两次。据我们所知,这是首次明确报道鉴定出台湾大豆荚和茎疫病的病原菌。受感染标本的凭证保存在亚洲蔬菜研究与发展中心。参考文献:(1)R. P. Mulrooney。《植物病害》70:600,1988年。(2)R. N. Pioli等人。《植物病理学》93:136,2003年。(3)A. W. Zhang等人。《植物病理学》88:1306,1998年。