Mahmooli I H Al, Balushi F Al, Doyle O, Sadi A M Al, Deadman M L
Department of Crop Sciences, Sultan Qaboos University, P.O. Box 34, Al Khod 123, Sultanate of Oman.
Royal Court Affairs, P.O. Box 17, Muscat 111, Sultanate of Oman.
Plant Dis. 2013 Feb;97(2):284. doi: 10.1094/PDIS-03-12-0233-PDN.
Hybrid gladiolus varieties have potential as a major ornamental crop in Oman. Grown for the cut-flower industry, their production has increased significantly in recent years. In 2010, during a field trial of two hybrid varieties (Red Majesty and Mascagni) grown in sandy soil at Al Moballah, Muscat, approximately 3% of Red Majesty plants and 12% of Mascagni plants showed signs of wilting and yellowing prior to plant death. In all cases, tissue taken from 20 diseased corms yielded Fusarium-like colonies on potato dextrose agar (PDA). Colonies were light to dark purple in color with dense and abundant aerial mycelium; macroconidia were 33.8 × 4.8 μm with 3 to 5 septa per spore; microconidia were 13.5 × 4.8 μm with 0 to 1 septa per spore and were in chains (mean of 50 spores in both cases). No chlamydospores were observed. In vitro characters and spore measurements conformed to previously described features of Fusarium proliferatum (Matsushima) Nirenberg (2). Mycelial plugs (5 mm in diameter) were taken from 5-day-old cultures of F. proliferatum grown on 2.5% PDA and wrapped on the base of Gladiolus corms using Parafilm and wet cotton. The Parafilm was removed after 7 days of inoculation. The corms were kept in moistened polythene bags for and symptoms were recorded. Control corms were inoculated using PDA (1). Artificial inoculations resulted in rot symptoms on all corms within 14 days and fungal colonies identical to initial isolations were recovered from artificially infected corms. Rotting was not observed in corms inoculated using PDA alone. Identification of F. proliferatum was confirmed using sequences of the internal transcribed spacer (ITS) of the ribosomal DNA (ITS1 and ITS4 primers) and sequences of the translation elongation factor alpha (TEF-1) gene (EF-1-986 and EF-728 primers). The ITS and TEF-1 sequences were found to share 99.8% and 99.6% nucleotide similarity to previously published sequences of the ITS (HQ113948) and EF (JN092351) regions of F. proliferatum in GenBank, respectively. The ITS sequence of one isolate was assigned GenBank Accession No. JN86006. To our knowledge, this is the first report of the occurrence of F. proliferatum in Oman or in the Arabian Peninsula. References: (1) C. Linfield. Ann. Appl. Biol. 121:175, 1983. (2) P. E. Nelson et al. Fusarium Species: An Illustrated Manual for Identification. Pennsylvania State University Press, USA, 1983.
杂交唐菖蒲品种有潜力成为阿曼的一种主要观赏作物。它们为切花产业而种植,近年来其产量显著增加。2010年,在马斯喀特穆巴拉的沙地对两个杂交品种(红皇后和马斯卡尼)进行田间试验期间,红皇后植株约3%以及马斯卡尼植株约12%在植株死亡前出现萎蔫和黄化迹象。在所有情况下,从20个患病球茎上取下的组织在马铃薯葡萄糖琼脂(PDA)上产生了类似镰刀菌的菌落。菌落颜色从浅紫色到深紫色,气生菌丝浓密且丰富;大型分生孢子为33.8×4.8μm,每个孢子有3至5个隔膜;小型分生孢子为13.5×4.8μm,每个孢子有0至1个隔膜,呈链状(两种情况下平均每条链有50个孢子)。未观察到厚垣孢子。体外特征和孢子测量结果与先前描述的轮枝镰孢(松岛)尼伦伯格的特征相符(2)。从在2.5%PDA上生长5天的轮枝镰孢培养物中取出直径5毫米的菌丝块,用 parafilm 和湿棉花包裹在唐菖蒲球茎基部。接种7天后取下parafilm。将球茎保存在湿润的聚乙烯袋中并记录症状。对照球茎接种PDA(1)。人工接种导致所有球茎在14天内出现腐烂症状,并且从人工感染的球茎中分离出与最初分离物相同的真菌菌落。仅接种PDA的球茎未观察到腐烂。使用核糖体DNA的内部转录间隔区(ITS)序列(ITS1和ITS4引物)以及翻译延伸因子α(TEF - 1)基因序列(EF - 1 - 986和EF - 728引物)确认了轮枝镰孢的鉴定。发现ITS和TEF - 1序列与GenBank中先前公布的轮枝镰孢ITS(HQ113948)和EF(JN092351)区域序列分别具有99.8%和99.6%的核苷酸相似性。一个分离株的ITS序列被赋予GenBank登录号JN86006。据我们所知,这是轮枝镰孢在阿曼或阿拉伯半岛发生的首次报道。参考文献:(1)C. Linfield。《应用生物学年报》121:175,1983。(2)P. E. Nelson等人。《镰刀菌物种:鉴定图谱手册》。美国宾夕法尼亚州立大学出版社,1983。