Ahonsi M O, Agindotan B O, Williams D W, Arundale R, Gray M E, Voigt T B, Bradley C A
Energy Biosciences Institute, University of Illinois, Urbana 61801.
Department of Plant and Soil Science, University of Kentucky, Lexington 40546.
Plant Dis. 2010 Apr;94(4):480. doi: 10.1094/PDIS-94-4-0480C.
Miscanthus × giganteus is a warm-season perennial grass, native to eastern Asia. Brought into the United States as a landscape plant, it is currently being considered as a potential biomass fuel crop. In August 2009, a newly established and a 2-year-old M. × giganteus field research trial near Lexington, KY were found to have 100% incidence of severe leaf blight. Brown, mosaic-like, coalesced necrotic lesions covered leaf blades and sheaths on every stand, ultimately killing some leaves and tillers. The disease was more destructive in the newly established trial where 4- to 5-month-old M. × giganteus tillers were killed. No fruiting bodies were found immediately on diseased leaves. However, surface-disinfested diseased leaf tissue produced a sooty black mass of conidia after 1 week following incubation in a petri dish moisture chamber at 25°C in the dark. Single conidia isolations were made on half-strength potato dextrose agar (HSPDA) amended with 25 mg/liter of rifamycin and incubated at 25°C. Morphological characteristics of the fungus fit those originally described for Pithomyces chartarum (Berk. & Curt.) M.B. Ellis (2). Colonies were fast growing on HSPDA, at first hyaline, then shortly punctiform, grayish black, up to 1-mm diameter, and then became confluent, producing several dark brown multicellular conidia on small peg-like denticles on branched conidiophores. Every detached conidium had a small piece of the denticle attached to its base. The conidia were echinulate, broadly ellipsoidal, pyriform, 18 to 29 × 11 to 18 μm, with three transverse septa, and a longitudinal septum constricted at the transverse septa. The identity of the fungus was confirmed by sequence analysis of the internal transcribed spacers (ITS) region of the nuclear ribosomal DNA. The 615-bp cloned and sequenced amplicon (Accession No. GU195649) was 99% identical to sequences from multiple isolates of Leptosphaerulina chartarum (anamorph Pithomyces chartarum) in the GenBank. Five potted M. × giganteus plants (45 days old) were spray inoculated with an aqueous conidial suspension (2 × 10 conidia/ml) and incubated in one tier of a two-tiered-growth chamber at 86 to 90% relative humidity. Initial incubation was in the dark at 26°C for 48 h, and thereafter at alternating 15 h of light (320 μmol) at 25°C and 9 h of darkness at 23°C. Control plants were sprayed with sterile water and incubated in the second tier of the same growth chamber. A week after inoculation, leaf blight developed on all inoculated plants, but not the controls. P. chartarum was reisolated from infected leaves 2 weeks after inoculation. To our knowledge, this is the first report of P. chartarum causing a disease on Miscanthus (3). The fungus is cosmopolitan, usually saprophytic, but can cause diseases on a wide range of plants as well as produce mycotoxins (3). It has been reported to cause a leaf spot of smooth bromegrass (Bromus inermis) in Nebraska (1) and a leaf blight of wheat (Triticum aestivum) in Hungary (4). The observed disease severity suggests P. chartarum could potentially limit M. × giganteus production as an ethanol feedstock. References: (1) C. Eken et al. Plant Dis. 90:108, 2006. (2) M. B. Ellis. Dematiaceous Hyphomycetes. Commonwealth Mycological Institute, Kew, Surrey, England, 1971. (3) D. F. Farr et al. Fungal Databases, Systematic Mycology and Microbiology Laboratory. Online publication. ARS, USDA, 2010. (4) B. Tóth et al. J. Plant Pathol. 89:405, 2007.
巨芒草是一种暖季型多年生草本植物,原产于东亚。它作为一种园林植物被引入美国,目前正被视作一种潜在的生物质燃料作物。2009年8月,在肯塔基州列克星敦附近一块新种植的以及一块种植了两年的巨芒草田间研究试验田被发现严重叶枯病发病率达100%。棕色、类似花叶病的、融合的坏死病斑覆盖了每个试验田的叶片和叶鞘,最终致使一些叶片和分蘖死亡。在新种植的试验田中病害更具毁灭性,4至5月龄的巨芒草分蘖死亡。在患病叶片上未立即发现子实体。然而,经表面消毒的患病叶片组织在25°C黑暗条件下于培养皿湿度箱中培养1周后产生了一团煤烟色的分生孢子。在添加了25毫克/升利福霉素的半强度马铃薯葡萄糖琼脂(HSPDA)上进行单分生孢子分离,并在25°C下培养。该真菌的形态特征与最初描述的皮思霉(Berk. & Curt.)M.B. 埃利斯(2)相符。菌落在HSPDA上生长迅速,起初无色透明,随后很快呈点状,灰黑色,直径达1毫米,然后融合,在分枝分生孢子梗上的小钉状小齿上产生几个深棕色多细胞分生孢子。每个分离的分生孢子基部都附着有一小片小齿。分生孢子具刺,宽椭圆形,梨形,18至29×宽椭圆11至18微米,有三个横向隔膜,以及一个在横向隔膜处缢缩的纵向隔膜。通过对核糖体DNA的内部转录间隔区(ITS)区域进行序列分析确认了该真菌的身份。克隆并测序的615碱基对扩增子(登录号GU195649)与GenBank中多个稻瘟病菌(无性型皮思霉)分离株的序列有99%的同一性。五株盆栽巨芒草植株(45日龄)用分生孢子水悬浮液(2×10分生孢子/毫升)喷雾接种,并在两层生长室的一层中于相对湿度86%至90%下培养。最初在26°C黑暗中培养48小时,此后在25°C下交替进行15小时光照(320微摩尔)和23°C下9小时黑暗培养。对照植株用无菌水喷雾并在同一生长室的第二层中培养。接种一周后,所有接种植株上出现叶枯病,而对照植株未出现。接种两周后从感染叶片中重新分离出皮思霉。据我们所知,这是皮思霉在巨芒草上引起病害的首次报道(3)。该真菌分布广泛,通常为腐生菌,但也可在多种植物上引起病害并产生霉菌毒素(3)。据报道它在内布拉斯加州引起了无芒雀麦(Bromus inermis)的叶斑病(1),在匈牙利引起了小麦(Triticum aestivum)的叶枯病(4)。观察到的病害严重程度表明皮思霉可能会限制巨芒草作为乙醇原料的生产。参考文献:(1)C. 埃肯等人,《植物病害》90:108,2006年。(2)M.B. 埃利斯,《暗色丝孢菌》,英国萨里郡邱园皇家植物园真菌研究所,1971年。(3)D.F. 法尔等人,《真菌数据库》,系统真菌学与微生物学实验室。在线出版物。美国农业部农业研究局,2010年。(4)B. 托特等人,《植物病理学杂志》89:405,2007年。