Pei Dongli, Zhang Qingchen, Zhang Yuyang, Zhang Mengfei, Lv Hongyi
Shangqiu Normal University, Shangqiu 476000, Henan, P.R. ChinaShangqiu, China, 476000;
Shangqiu , China;
Plant Dis. 2022 Jun 9. doi: 10.1094/PDIS-01-22-0214-PDN.
Glandularia tenera (syn. Verbena tenera) is an herbaceous perennial ornamental plant used in gardens as an edging plant with beautiful white, red, or purple flowers. In autumn 2020 and 2021, severe powdery mildew infection was observed on G. tenera cultivar Xianghe in Renming Botanical garden in Shangqiu, Henan province, China (34.4568° N, 115.6640° E). Approximately 80% of leaves on each plant were symptomatic, and about 90% of the plants were infected. Powdery mildew colonies appeared as white spots on the adaxial surface of the leaves and stems of the plants in the initial infection stage. Later, mycelial growth was amphigenous, thick, forming irregular white patches, and effused to cover the whole leaf surface. Finally, leaves turned yellow and senescence occurred. Samples of symptomatic leaves were stained with trypan blue and examined under a Leica DM2500 microscope. Microscopic observations showed that conidia on infected leaves were hyaline and ellipsoid to oval with fibrosin bodies, measured 25 to 37 × 14 to 23 μm with a length/width ratio of 1.4 to 2.0. Conidiophores were unbranched, straight, 80 to 210× 10 to 14 µm in size, and produced two to five immature conidia in chains. Foot cells of conidiophores were cylindrical with slight constrictions at basal septa, and followed by one to three short cells. Fungal hyphae were septate, branched, and flexuous to straight and 4 to 7µm wide with indistinct to slightly nipple-shaped appressoria. Chasmothecia were not observed. These morphological characteristics were identical with the previous description of Podosphaera xanthii (Castagne) U. Braun & Shishkoff (Braun and Cook 2012). To confirm the identification, the sequence of ITS1-5.8s-ITS2 region of rDNA for the isolate SQVT was amplified from conidia collected from infected leaves with universal primers ITS1 and ITS4, sequenced and analyzed using the BLASTn search of GenBank. Amplicon was 565 bp (OM293967) and showed 99.82% similarity with sequence of P. xanthii from Eclipta prostrate (MT260063) in China (Xu et al. 2020), from Youngia denticulate (AB040351) in Japan (Hirata et al. 2000), and 99.65% with sequence of P. xanthii from V. brasiliensis in Korea (Cho et al. 2014). The domains D1 and D2 of the 28S rDNA for the isolate SQVTPX-1 was amplified with primer NL1/NL4. Amplicon was 613 bp (ON259308) and showed 100% similarity with sequence of P. xanthii from V. brasiliensis (AB936277) (Meeboon and Takamatsu, 2015). Pathogenicity tests were conducted by gently pressing the infected leaves onto leaves of five healthy G. tenera cultivar Xianghe plants. Five non-inoculated plants served as controls. Plants were maintained in a greenhouse at 25 ± 2°C. Eight days after inoculation, symptoms similar to those observed under natural conditions developed on the inoculated leaves of G. tenera plants, whereas the control plants remained symptomless. The fungus on inoculated leaves was morphologically identical to that first observed in the field. P. xanthii is a cosmopolitan powdery mildew fungus, parasitic on numerous plant species, especially Cucurbitaceae and Compositae plants. The pathogen has been reported infecting V. bonariensis (Hong et al. 2021), V. × hybrida in China (Zhuang 2005), and V. brasiliensis in Korea (Cho et al. 2014). Interestingly, G. tenera plants infected by P. xanthii were adjacent with V. × hybrida plants infected by P. xanthii in Renming Botanical garden. Incidence of P. xanthii on G. tenera add information on pathogen's host range and help us develop comprehensive survey and effective management of the disease. To our knowledge, this is the first report of P. xanthii on G. tenera in China (Farr and Rossman 2021). Braun, U., and Cook, R. T. A. 2012. Taxonomic Manual of the Erysiphales (Powdery Mildews). CBS Biodiversity Series No. 11. CBS, Utrecht, the Netherlands. Cho, S. E., et al. 2014. Plant Dis. 98: 1159. Farr, D. F., and Rossman, A. Y. 2021. Fungal Databases, Syst. Mycol. Microbiol. Lab., ARS, USDA. Hong, Q. Q., et al. 2021. Plant Dis. 105: 3297. Hirata, T., et al. 2000. Can. J. Bot. 78: 1521-1530. Meeboon, J. and Takamatsu, S. 2015. Mycoscience . 56: 243-251. Xu, D. D., et al. 2020. Plant Dis. 104: 3263. Zhuang, W. Y. 2005. Fungi of northwestern China. Mycotaxon, Ltd., Ithaca, NY.
柔弱腺毛草(学名:Glandularia tenera,异名:Verbena tenera)是一种多年生草本观赏植物,在园林中用作边缘植物,开有美丽的白色、红色或紫色花朵。2020年秋季和2021年,在中国河南省商丘市人民植物园(北纬34.4568°,东经115.6640°),柔弱腺毛草品种香河上观察到严重的白粉病感染。每株植物约80%的叶片出现症状,约90%的植株被感染。在初始感染阶段,白粉病菌落出现在植株叶片和茎的正面,呈白色斑点。后来,菌丝体两面生,浓密,形成不规则的白色斑块,并蔓延覆盖整个叶片表面。最后,叶片变黄并发生衰老。对有症状的叶片样本用台盼蓝染色,并在徕卡DM2500显微镜下检查。显微镜观察表明,感染叶片上的分生孢子无色透明,椭圆形至卵形,有纤维状内含体,大小为25至37×14至23μm,长宽比为1.4至2.0。分生孢子梗不分枝,直立,大小为80至210×10至14μm,链生2至5个未成熟分生孢子。分生孢子梗的基部细胞圆柱形,基部隔膜处略有缢缩,其后是1至3个短细胞。真菌菌丝有隔膜,分枝,弯曲至直立,宽4至7μm,附着胞不明显至略呈乳头状。未观察到闭囊壳。这些形态特征与之前对瓜单囊壳白粉菌(学名:Podosphaera xanthii (Castagne) U. Braun & Shishkoff)的描述一致(布劳恩和库克,2012年)。为了确认鉴定结果,使用通用引物ITS1和ITS4从感染叶片上收集的分生孢子中扩增出分离株SQVT的rDNA的ITS1-5.8s-ITS2区域序列,进行测序并使用GenBank的BLASTn搜索进行分析。扩增片段为565bp(OM293967),与中国来自鳢肠(学名:Eclipta prostrate,登录号:MT260063)(徐等人,2020年)、日本来自齿缘苦荬菜(学名:Youngia denticulate,登录号:AB040351)(平田等人,2000年)的瓜单囊壳白粉菌序列相似度为99.82%,与韩国来自巴西马鞭草(学名:V. brasiliensis)的瓜单囊壳白粉菌序列相似度为99.65%(赵等人,2014年)。使用引物NL1/NL4扩增分离株SQVTPX-1的28S rDNA的D1和D2结构域。扩增片段为613bp(ON259308),与来自巴西马鞭草(登录号:AB936277)的瓜单囊壳白粉菌序列相似度为百分之百(米本和高松,2015年)。通过将感染叶片轻轻压在五株健康的柔弱腺毛草品种香河植株的叶片上进行致病性测试。五株未接种的植株作为对照。植株在25±2°C的温室中养护。接种八天后,柔弱腺毛草接种叶片上出现了与自然条件下观察到的症状相似的症状,而对照植株仍无症状。接种叶片上的真菌在形态上与最初在田间观察到的真菌相同。瓜单囊壳白粉菌是一种世界性的白粉菌真菌,寄生于许多植物物种,尤其是葫芦科和菊科植物。该病原菌已被报道感染阿根廷马鞭草(洪等人,2021年)、中国的杂交马鞭草(庄,200伍年)以及韩国的巴西马鞭草(赵等人,2014年)。有趣的是,在人民植物园中,被瓜单囊壳白粉菌感染的柔弱腺毛草植株与被瓜单囊壳白粉菌感染的杂交马鞭草植株相邻。瓜单囊壳白粉菌在柔弱腺毛草上的发生情况为病原菌的寄主范围提供了信息,并有助于我们开展该病的综合调查和有效管理。据我们所知, 这是中国首次报道瓜单囊壳白粉菌感染柔弱腺毛草(法尔和罗斯曼,2021年)。
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