Vakalounakis D J, Markakis E A
Laboratory of Phytopathological Mycology, Plant Protection Institute, Hellenic Agricultural Organization "Demeter", P.O. Box 2228, 710 03 Heraklio, Greece.
Plant Dis. 2013 Feb;97(2):287. doi: 10.1094/PDIS-08-12-0776-PDN.
During the 2011 to 2012 crop season, a severe leaf spot disease of cucumber (Cucumis sativus) cv. Cadiz was noticed on crops in some greenhouses in the Goudouras area, Lasithi, Crete, Greece. Symptoms appeared in late winter, mainly on the leaves of the middle and upper part of the plants. Initially, small necrotic pinpoint lesions with white centers, surrounded by chlorotic halos, 1 to 3 mm in diameter, appeared on the upper leaf surfaces, and these progressively enlarged to spots that could coalesce to form nearly circular lesions up to 2 cm or more in diameter. Stemphylium-like fructifications appeared on necrotic tissue of older lesions. Severely affected leaves became chlorotic and died. No other part of the plant was affected. Small tissue pieces from the edges of lesions were surface disinfected in 0.5% NaClO for 5 min, rinsed in sterile distilled water, plated on acidified potato dextrose agar and incubated at 22 ± 0.5°C with a 12-h photoperiod. Stemphylium sp. was consistently isolated from diseased samples. Colonies showed a typical septate mycelium with the young hyphae subhyaline and gradually became greyish green to dark brown with age. Conidiophores were subhyaline to light brown, 3- to 10-septate, up to 200 μm in length, and 4 to 7 μm in width, with apical cell slightly to distinctly swollen, bearing a single spore at the apex. Conidia were muriform, mostly oblong to ovoid, but occasionally nearly globose, subhyline to variant shades of brown, mostly constricted at the median septum, 22.6 ± 6.22 (11.9 to 36.9) μm in length, and 15.1 ± 2.85 (8.3 to 22.6) μm in width, with 1 to 8 transverse and 0 to 5 longitudinal septa. DNA from a representative single-spore isolate was extracted and the internal transcribed spacer region (ITS) of ribosomal DNA (rDNA) was amplified using the universal primers ITS5 and ITS4. The PCR product was sequenced and deposited in GenBank (Accession No. JX481911). On the basis of morphological characteristics (3) and a BLAST search with 100% identity to the published ITS sequence of a S. solani isolate in GenBank (EF0767501), the fungus was identified as S. solani. Pathogenicity tests were performed by spraying a conidial suspension (10 conidia ml) on healthy cucumber (cv. Knossos), melon (C. melo, cv. Galia), watermelon (Citrullus lanatus cv. Crimson sweet), pumpkin (Cucurbita pepo, cv. Rigas), and sponge gourd (Luffa aegyptiaca, local variety) plants, at the 5-true-leaf stage. Disease symptoms appeared on cucumber and melon only, which were similar to those observed under natural infection conditions on cucumber. S. solani was consistently reisolated from artificially infected cucumber and melon tissues, thus confirming Koch's postulates. The pathogenicity test was repeated with similar results. In 1918, a report of a Stemphylium leaf spot of cucumber in Indiana and Ohio was attributed to Stemphylium cucurbitacearum Osner (4), but that pathogen has since been reclassified as Leandria momordicae Rangel (2). That disease was later reported from Florida (1) and net spot was suggested as a common name for that disease. For the disease reported here, we suggest the name Stemphylium leaf spot. This is the first report of a disease of cucumber caused by a species of Stemphylium. References: (1) C. H. Blazquez. Plant Dis. 67:534, 1983. (2) P. Holliday. Page 243 in: A Dictionary of Plant Pathology. Cambridge University Press, Cambridge, UK, 1998. (3) B. S. Kim et al. Plant Pathol. J. 15:348, 1999. (4) G. A. Osner. J. Agric. Res. 13:295, 1918.
在2011至2012年作物生长季,希腊克里特岛拉西锡州古多拉地区的一些温室黄瓜(Cucumis sativus)品种卡迪兹上出现了一种严重的叶斑病。症状在冬末出现,主要出现在植株中上部叶片上。最初,叶片上表面出现直径1至3毫米的小坏死点状病斑,病斑中心白色,周围有褪绿晕圈,这些病斑逐渐扩大成斑点,可融合形成直径达2厘米或更大的近圆形病斑。在较老病斑的坏死组织上出现类似匍柄霉属的子实体。严重受害叶片褪绿并死亡。植株的其他部分未受影响。从病斑边缘取小组织块,在0.5%次氯酸钠中进行表面消毒5分钟,用无菌蒸馏水冲洗后,接种在酸化马铃薯葡萄糖琼脂上,于22±0.5°C、12小时光周期下培养。始终能从患病样本中分离出匍柄霉属真菌。菌落呈现典型的具隔膜菌丝体,幼嫩菌丝近无色,随着生长逐渐变为灰绿色至深褐色。分生孢子梗近无色至浅褐色,具3至10个隔膜,长达200微米,宽4至7微米,顶端细胞稍肿胀至明显肿胀,顶端着生单个孢子。分生孢子为砖格状,大多长圆形至卵形,但偶尔近球形,近无色至不同深浅的褐色,大多在中间隔膜处缢缩,长22.6±6.22(11.9至36.9)微米,宽15.1±2.85(8.3至22.6)微米,具1至8个横向隔膜和0至5个纵向隔膜。提取来自一个代表性单孢子分离物的DNA,使用通用引物ITS5和ITS4扩增核糖体DNA(rDNA)的内部转录间隔区(ITS)。PCR产物进行测序并提交至GenBank(登录号JX481911)。根据形态特征(3)以及与GenBank中已发表的茄匍柄霉分离物ITS序列(EF0767501)100%同源的BLAST搜索结果,该真菌被鉴定为茄匍柄霉。通过在5片真叶期的健康黄瓜(品种克诺索斯)、甜瓜(C. melo,品种加利亚)、西瓜(Citrullus lanatus品种深红甜蜜)、南瓜(Cucurbita pepo,品种里加斯)和丝瓜(Luffa aegyptiaca,当地品种)植株上喷洒分生孢子悬浮液(10个分生孢子/毫升)进行致病性测试。仅在黄瓜和甜瓜上出现病害症状,这些症状与在黄瓜自然感染条件下观察到的症状相似。始终能从人工感染的黄瓜和甜瓜组织中重新分离出茄匍柄霉,从而证实了柯赫氏法则。重复进行致病性测试,结果相似。1918年,印第安纳州和俄亥俄州有一份关于黄瓜匍柄霉叶斑病的报告,该病被归因于瓜匍柄霉(Stemphylium cucurbitacearum Osner)(4),但该病原菌后来被重新分类为苦瓜链格孢(Leandria momordicae Rangel)(2)。后来佛罗里达州也报道了该病(1),并建议将净斑病作为该病的通用名称。对于此处报道的病害,我们建议命名为匍柄霉叶斑病。这是由匍柄霉属物种引起的黄瓜病害的首次报道。参考文献:(1)C. H. Blazquez。植物病害。67:534,1983。(2)P. Holliday。见:植物病理学词典。英国剑桥大学出版社,剑桥,1998年,第243页。(3)B. S. Kim等人。植物病理学杂志。15:348,1999。(4)G. A. Osner。农业研究杂志。13:295,1918。