Koike S T
University of California Cooperative Extension, Salinas 93901.
Plant Dis. 1997 Nov;81(11):1331. doi: 10.1094/PDIS.1997.81.11.1331B.
In 1997, greenhouse-produced transplants of watermelon (Citrullus lanatus) developed water-soaked lesions on leaf petioles and main stems. As disease progressed, petioles and stems became necrotic and shriveled, and exuded a sticky, translucent tan liquid. Symptoms spread to leaves, which wilted and collapsed. Affected transplants eventually died. Although fruiting bodies were not observed on diseased plants, a fungal agent was consistently isolated from symptomatic tissues. When incubated under lights (12 h light/12 h dark cycle), isolates on potato dextrose agar produced numerous pycnidia with hyaline, cylindrical, one-septate conidia with mean dimensions of 5.6 × 2.8 μm. Under the same incubation conditions, isolates on V8 juice agar produced sparse ostiolate pseudothecia with bitunicate asci and hyaline, oval, one-septate ascospores with mean dimensions of 12.0 × 4.0 μm. Based on these characters, the isolates were identified as Didymella bryoniae (anamorph Phoma cucurbitacearum) (1,2). Pathogenicity was tested by producing conidial inocula of representative isolates and inoculating wounded cotyledons, true leaves, and petioles of watermelon (cv. Sangria), and wounded true leaves and petioles of cucumber (Cucumis sativus cv. Premier Hybrid) (3). Sterile, distilled water was applied to corresponding wounded tissues of control plants. All plants were kept in a humid chamber for 4 days. After 6 (watermelon) to 10 (cucumber) days, inoculated plants exhibited water-soaked lesions followed by necrosis, petiole and leaf wilting, and shriveling of tissues. Pycnidia were observed on cucumber plants after 18 days. The pathogen was reisolated from all inoculated plants and identified as D. bryoniae. Control plants developed no disease symptoms. In addition, agar plugs colonized with the watermelon isolates were placed onto cucumber fruit that were wounded slightly with a sterile scalpel. Fruit were incubated at 22 to 24°C in humid chambers and after 2 days sunken, circular lesions developed. The same pathogen was reisolated from the margins of fruit lesions. Wounded control fruit received sterile agar plugs and did not develop any symptoms. This is the first documentation of gummy stem blight on watermelon transplants in California. References: (1) W. F. Chiu and J. C. Walker. J. Agric. Res. 78:81, 1949. (2) A. P. Keinath et al. Phytopathology 85:364, 1995. (3) A. J. Wyszogrodzka et al. Euphytica 35:603, 1986.
1997年,温室培育的西瓜(西瓜属)植株的叶柄和主茎上出现了水渍状病斑。随着病情发展,叶柄和茎干坏死并萎缩,渗出一种粘性、半透明的黄褐色液体。症状蔓延至叶片,叶片枯萎并倒伏。受影响的植株最终死亡。尽管在患病植株上未观察到子实体,但从症状组织中始终分离出一种真菌病原体。在光照条件下(12小时光照/12小时黑暗周期)培养时,马铃薯葡萄糖琼脂培养基上的分离菌产生了大量的分生孢子器,其分生孢子透明、圆柱形、具一个隔膜,平均尺寸为5.6×2.8微米。在相同培养条件下,V8果汁琼脂培养基上的分离菌产生了少量具孔口的假囊壳,其囊壁双层,子囊孢子透明、椭圆形、具一个隔膜,平均尺寸为12.0×4.0微米。根据这些特征,分离菌被鉴定为黄瓜壳二孢菌(无性型为葫芦科茎点霉)(1,2)。通过制备代表性分离菌的分生孢子接种物,并接种西瓜(品种Sangria)的受伤子叶、真叶和叶柄,以及黄瓜(品种Premier Hybrid)的受伤真叶和叶柄,来测试致病性(3)。将无菌蒸馏水施用于对照植株相应的受伤组织。所有植株置于潮湿培养箱中4天。6(西瓜)至10(黄瓜)天后,接种植株出现水渍状病斑,随后坏死、叶柄和叶片枯萎以及组织萎缩。18天后在黄瓜植株上观察到分生孢子器。从所有接种植株中重新分离出病原体,并鉴定为黄瓜壳二孢菌。对照植株未出现病害症状。此外,将接种有西瓜分离菌的琼脂块放置在用无菌手术刀轻微划伤的黄瓜果实上。果实于22至24°C在潮湿培养箱中培养,2天后出现凹陷的圆形病斑。从果实病斑边缘重新分离出相同的病原体。受伤的对照果实接受无菌琼脂块,未出现任何症状。这是加利福尼亚州西瓜植株上首次记录到的蔓枯病。参考文献:(1)W. F. Chiu和J. C. Walker。《农业研究杂志》78:81,1949年。(2)A. P. Keinath等人。《植物病理学》85:364,1995年。(3)A. J. Wyszogrodzka等人。《欧洲植物病理学报》35:603,1986年。