McLeod A, Coertze S
University of Stellenbosch, Department of Plant Pathology, Private Bag X1, Matieland 7602, South Africa.
Plant Dis. 2006 Dec;90(12):1550. doi: 10.1094/PD-90-1550B.
Phytophthora infestans is known worldwide as the destructive, late blight pathogen of potatoes and tomatoes. However, erratic reports dating back to 1856 also have shown it to be pathogenic on petunia (Petunia × hybrida), although it has not been regarded as an important pathogen on this host (4). Recently, reports from North America showed that P. infestans is of commercial importance in greenhouse-grown petunias (2), and that late blight-infected petunias may serve as inoculum to tomatoes growing in the same greenhouse (1,2). In the Western Cape Province of South Africa, two petunia samples were received at the Stellenbosch University Plant Disease Clinic in 2005 that showed symptoms resembling P. infestans infections. The two samples were from nurseries where petunias were either grown under shading nets or in a greenhouse. In the greenhouse-grown petunias, the presumptive late blight infections resulted in substantial losses to the grower. Symptoms included gray, slightly sunken leaf lesions with white sporulation mainly on the adaxial side of the leaves. Leaflets of the petunias were incubated in moist chambers, and sporangia sporulating from lesions were identified morphologically as being P. infestans (3). Subsequently, one isolate was cultured onto synthetic media by carefully transferring sporangia from a lesion with the tip of a bended glass rod onto wheat medium (120 g/L of crushed wheat seeds, blended, boiled and filtered through cheesecloth, plus 15 g of sucrose and agar). The identity of the culture was further confirmed through sequence analyses of the internal transcribed spacer regions (GenBank Accession No. DQ479409). The isolated P. infestans strain (STE-U 6134) has been submitted to the Stellenbosch University culture collection. Inoculum for the pathogenicity tests was produced by first flooding 14-day-old cultures with sterile distilled water to obtain a 2 × 10/ml sporangial suspension, followed by zoospore induction at 4°C. A mixture of petunia cultivars (n = 24) were spray inoculated to runoff with the zoospore induced sporangial suspension. Control plants were sprayed with sterile distilled water. Inoculated plants were incubated at 22 to 25°C and high relative humidity (≥93%) within perspex humidity chambers (60 × 30 × 60 cm) lined with a wet sheet of chromatography paper. The experiment was repeated twice. The first late blight symptoms similar to those of the submitted samples appeared 5 to 7 days after inoculation, with some lesions containing profuse white mycelia and sporangiophores typical for P. infestans. The pathogen was reisolated from the leaf lesions, completing Koch's postulate. To our knowledge, this is the first report of P. infestans causing damage on petunias in South Africa. Future studies should be aimed at investigating whether late blight-infected petunias provide an important source of inoculum for potatoes and tomatoes, which are widely grown in the Western Cape Province of South Africa. References: (1) M. C. Becktell et al. Plant Dis. 89:1000, 2005. (2) K. L. Deahl and D. K. Farel. Plant Dis. 87:1004, 2003. (3) D. C. Erwin and O. K. Ribeiro, Phytophthora Diseases Worldwide. The American Phytopathological Society St. Paul, MN, 1996. (4) J. M. Hirst and W. C. Moore. Phytophthora infestans on petunia and datura. Page 76 in: Plant Pathology-A Record of Current Work on Plant Diseases and Pests. Vol. 6. Ministry of Agriculture, Fisheries and Food Plant Pathology Laboratory, Harpenden, England, 1957.
致病疫霉在全球范围内被认为是马铃薯和番茄的毁灭性晚疫病病原菌。然而,可追溯到1856年的零散报告也表明它对矮牵牛(Petunia × hybrida)具有致病性,尽管它在该寄主上未被视为重要病原菌(4)。最近,来自北美的报告显示致病疫霉在温室种植的矮牵牛中具有商业重要性(2),并且晚疫病感染的矮牵牛可能作为同一温室中生长的番茄的接种源(1,2)。在南非西开普省,2005年斯泰伦博斯大学植物病害诊所收到了两个矮牵牛样本,其症状类似于致病疫霉感染。这两个样本来自矮牵牛种植于遮阳网下或温室中的苗圃。在温室种植的矮牵牛中,推定的晚疫病感染给种植者造成了重大损失。症状包括叶片上灰色、略凹陷的病斑,白色孢子主要出现在叶片正面。将矮牵牛小叶置于保湿箱中培养,从病斑上产生孢子囊的形态学鉴定为致病疫霉(3)。随后,通过用弯曲玻璃棒尖端从病斑小心转移孢子囊到小麦培养基(120 g/L碾碎的小麦种子,混合、煮沸并通过粗棉布过滤,加15 g蔗糖和琼脂)上,将一个分离株培养到合成培养基上。通过对内部转录间隔区的序列分析进一步确认了培养物的身份(GenBank登录号DQ479409)。分离出的致病疫霉菌株(STE-U 6134)已提交到斯泰伦博斯大学培养物保藏中心。致病性测试的接种物通过先用无菌蒸馏水淹没培养14天的培养物以获得2×10/ml的孢子囊悬浮液,然后在4°C下诱导游动孢子来制备。将矮牵牛品种混合物(n = 24)用诱导游动孢子的孢子囊悬浮液喷雾接种至径流。对照植株喷洒无菌蒸馏水。接种的植株在装有湿色谱纸的有机玻璃保湿箱(60×30×60 cm)中于22至25°C和高相对湿度(≥93%)下培养。该实验重复两次。接种后5至7天出现了与提交样本相似的首批晚疫病症状,一些病斑含有大量典型的致病疫霉白色菌丝体和孢子梗。从叶片病斑中重新分离出病原菌,完成了柯赫氏法则验证。据我们所知,这是致病疫霉在南非对矮牵牛造成损害的首次报告。未来的研究应旨在调查晚疫病感染的矮牵牛是否为南非西开普省广泛种植的马铃薯和番茄提供重要的接种源。参考文献:(1)M. C. Becktell等人,《植物病害》89:1000,2005年。(2)K. L. Deahl和D. K. Farel,《植物病害》87:1004,2003年。(3)D. C. Erwin和O. K. Ribeiro,《全球疫霉病害》。美国植物病理学会,明尼苏达州圣保罗,1996年。(4)J. M. Hirst和W. C. Moore,《矮牵牛和曼陀罗上的致病疫霉》。载于:《植物病理学——植物病害和害虫当前研究记录》第6卷。农业、渔业和食品部植物病理实验室,英国哈彭登,1957年,第76页。