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意大利大戟属植物苏姗大戟和无刺大戟上的白粉菌属真菌。

Podosphaera sp. on Euphorbia susannae and E. inermis in Italy.

作者信息

Garibaldi A, Bertetti D, Pensa P, Poli A, Gullino M L

机构信息

Centre of Competence AGROINNOVA, University of Torino, Via Leonardo da Vinci 44, 10095 Grugliasco, Italy.

出版信息

Plant Dis. 2012 Dec;96(12):1824. doi: 10.1094/PDIS-06-12-0569-PDN.

Abstract

Euphorbia susannae (common name Suzane's spurge) and E. inermis (Euphorbiaceae family) are grown in pots and commercialized in northern Italy. In March 2012, plants of these species grown on the same commercial farm showed signs of powdery mildew. On E. susannae, apexes of stems were covered with white mycelia and conidia, with the ultimate development of necrosis on symptomatic tissues more interested by the disease. Of 5,000 plants, 5% were affected. Conidia were hyaline, elliptical, borne in short chains (two to three conidia per chain), and 27.7 (24.4 to 30.6) μm long and 16.1 (13.6 to 19.1) μm wide. Conidiophores were erect, with a foot cell straight or slightly flexuous, 82.8 (52.7 to 117.1) μm long and 10.0 (9.2 to 11.2) μm wide, followed by two to three shorter cells 19.8 (14.7 to 28.9) μm long and 10.7 (8.7 to 13.0) μm wide. On E. inermis, a white mycelium covered the stems starting from the apexes, causing yellowing and necrosis on leaves finally killing infected tissues. Of 500 plants, 80% were affected. Conidia were 33.2 (25.7 to 42.0) μm long and 17.3 (12.6 to 21.6) μm wide. Conidiophores were erect, with a foot cell straight or slightly flexuous, 96.7 (67.0 to 138.6) μm long and 9.5 (7.7 to 11.7) μm wide, followed by two to three shorter cells 26.3 (17.5 to 42.2) μm long and 11.8 (8.3 to 16.2) μm wide. Fibrosin bodies were present on both hosts, while chasmothecia were not observed in samples from either host. The internal transcribed spacer (ITS) region of rDNA of samples of mycelium and conidia collected from the two hosts was amplified using the primers ITS1-ITS4 (3) and directly sequenced (GenBank Accession Nos. JX179221 and JX179219 for E. susannae and E. inermis, respectively). By performing BLAST analysis, the 692-bp amplicon from E. susannae and the 541-bp amplicon from E. inermis showed 100% homology with several sequences of Podosphaera spp. On the basis of morphological characteristics of the imperfect state and the ITS analysis, the causal agent of powdery mildew on E. susannae and E. inermis was identified as Podosphaera sp. Pathogenicity was confirmed by gently brushing healthy 20-month-old potted plants of E. susannae and E. inermis with mycelia and conidia from diseased plants. Four plants/treatment/species were used. Non-inoculated plants belonging to the two species served as control. Plants were maintained in a glasshouse at temperatures ranging from 18 to 25°C and relative humidity from 65 to 80%. About 20 days after inoculation, typical symptoms of powdery mildew developed on inoculated plants. The fungus observed on inoculated plants was morphologically identical to the original isolate. Non-inoculated plants did not exhibit symptoms. The pathogenicity test was performed in duplicate. Several agents of powdery mildew have been reported on Euphorbia spp. Among others, Podosphaera euphorbiae was reported on numerous Euphorbiaceae (1), P. euphorbiae-hirtae was observed on E. hirta (1) and P. euphorbiae-helioscopiae on E. pekinensis (2). To our knowledge, this is the first report of Podosphaera sp. on E. susannae and E. inermis in Italy. This disease is not presently of economic importance. Specimens are available at the Agroinnova Collection. References: (1) U. Braun. A Monograph of the Erysiphales (Powdery Mildews). J. Cramer, Berlin-Stuttgard, German Democratic Republic, 1987. (2) S. Y. Liu. Plant Dis. 95:1314, 2011. (3) T. J. White et al. PCR Protocols: A Guide to Methods and Applications. M. A. Innis et al., eds. Academic Press, San Diego, 1990.

摘要

苏珊大戟(俗名苏珊泽漆)和无刺大戟(大戟科)在意大利北部种植于花盆中并商业化销售。2012年3月,在同一个商业农场种植的这些物种的植株出现了白粉病症状。在苏珊大戟上,茎尖覆盖着白色菌丝体和分生孢子,症状组织上最终出现坏死,病害对其影响更大。在5000株植株中,5%受到影响。分生孢子无色透明,椭圆形,成短链着生(每条链有两到三个分生孢子),长27.7(24.4至30.6)μm,宽16.1(13.6至19.1)μm。分生孢子梗直立,基部细胞直或稍弯曲,长82.8(52.7至117.1)μm,宽10.0(9.2至11.2)μm,接着是两到三个较短的细胞,长19.8(14.7至28.9)μm,宽10.7(8.7至13.0)μm。在无刺大戟上,白色菌丝体从茎尖开始覆盖茎部,导致叶片发黄和坏死,最终使受感染组织死亡。在500株植株中,80%受到影响。分生孢子长33.2(25.7至42.0)μm,宽17.3(12.6至21.6)μm。分生孢子梗直立,基部细胞直或稍弯曲,长96.7(67.0至138.6)μm,宽9.5(7.7至11.7)μm,接着是两到三个较短的细胞,长26.3(17.5至42.2)μm,宽11.8(8.3至16.2)μm。两种寄主上均存在纤维状小体,而在两种寄主的样本中均未观察到闭囊壳。使用引物ITS1 - ITS4(3)对从两种寄主收集的菌丝体和分生孢子样本的rDNA内部转录间隔区(ITS)进行扩增,并直接测序(苏珊大戟和无刺大戟的GenBank登录号分别为JX179221和JX179219)。通过进行BLAST分析,苏珊大戟的692 bp扩增片段和无刺大戟的541 bp扩增片段与白粉菌属的几个序列显示出100%的同源性。根据不完全阶段的形态特征和ITS分析,确定苏珊大戟和无刺大戟上白粉病的病原菌为白粉菌属。通过用患病植株的菌丝体和分生孢子轻轻擦拭健康的20个月大的苏珊大戟和无刺大戟盆栽植株来证实致病性。每种处理/物种使用四株植株。两种物种的未接种植株作为对照。植株在温室中保持在18至25°C的温度和65至80%的相对湿度下。接种后约20天,接种植株上出现典型的白粉病症状。在接种植株上观察到的真菌在形态上与原始分离株相同。未接种植株未表现出症状。致病性试验重复进行。已经报道了几种大戟属植物上的白粉病病原菌。其中,在许多大戟科植物上报道了大戟白粉菌(1),在麻疯树大戟上观察到了麻疯树大戟白粉菌(1),在北京大戟上观察到了泽漆白粉菌(2)。据我们所知,这是意大利首次报道白粉菌属在苏珊大戟和无刺大戟上的情况。这种病害目前没有经济重要性。标本保存在农业创新收藏中。参考文献:(1)U. Braun.《白粉菌目(白粉病)专论》。J. Cramer,柏林 - 斯图加特,德意志民主共和国,1987年。(2)S. Y. Liu.《植物病害》95:1314,2011年。(3)T. J. White等人。《PCR协议:方法与应用指南》。M. A. Innis等人编。学术出版社,圣地亚哥,1990年。

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