Zale J, Freshour L, Agarwal S, Sorochan J, Ownley B H, Gwinn K D, Castlebury L A
Plant Sciences Department, University of Tennessee, 2431 Joe Johnson Drive, Knoxville 37996-4561.
Department of Entomology and Plant Pathology, University of Tennessee, 2431 Joe Johnson Drive, Knoxville 37996-4561.
Plant Dis. 2008 Dec;92(12):1710. doi: 10.1094/PDIS-92-12-1710B.
In the spring of 2007, switchgrass accessions and cultivars Alamo, Kanlow, SL-93-2001, and NSL 2001-1 (lowland), Blackwell (upland), and Grenville, Falcon, and Miami (unknown ploidy levels) were sown at the East Tennessee Research and Extension Center in Knoxville for evaluation and controlled hybridizations. In July and August of 2007, uredinia were observed primarily on the upper leaf surfaces, and to a lesser extent on the undersides of leaves, of switchgrass cvs. Alamo, Blackwell, Grenville, Falcon, Kanlow, and Miami. Uredinia were observed on all cultivars and accessions in 2008. Dimensions of spores are reported as mean ± standard deviation. Uredinia were epiphyllous, adaxial, caulicolous, oblong, and the color of cinnamon brown. Urediniospores were globose to broadly ellipsoid, 26.0 ± 3.0 × 23.2 ± 2.4 μm, with a wall that was cinnamon brown, 1.5 to 2.0 μm thick, finely echinulate with three to four equatorial pores, corresponding to Puccinia emaculata Schw. (3). Abundant teliospores were isolated from Grenville, Falcon, and Blackwell, with fewer teliospores isolated from Alamo. Telia were epiphyllous, adaxial, and caulicolous, densely crowded to scattered, oblong, and dark brown to black. Teliospores were dark brown, two-celled, ellipsoid to oblong, 33.6 ± 4.8 μm long with an apical cell width of 17.5 ± 1.2 μm and basal cell width of 15.9 ± 2.5 μm. Teliospore walls were 1.5 to 2.0 μm wide at the sides and 4 to 6 μm apically. Pedicels were brown or colorless and up to approximately one length of the teliospore, 28.5 ± 7.4 μm. Teliospore morphology confirmed the identification of this rust as P. emaculata (3), which has been reported to infect upland and lowland populations of switchgrass (2). A 2,109-bp fragment containing the internal transcribed spacer (ITS) 1, 5.8S, ITS 2, and D1/D2 region of the large subunit ribosomal DNA was sequenced for a specimen on 'Falcon' (GenBank Accession No. EU915294 and BPI No. 878722) from two overlapping PCR fragments amplified with primers PRITS1F (L. A. Castlebury, unpublished data) and ITS4B (1) for one fragment and Rust5.8SF (L. A. Castlebury, unpublished data) and LR7 (4) for the second fragment. No sequences of P. emaculata were available for comparison; however, BLAST searches of the ITS resulted in hits to P. asparagi DC (527 of 576, 91%) and P. andropogonis Schw. (523 of 568, 92%) placing this fungus in the genus Puccinia Pers. The alternate hosts of this rust are species of the Euphorbiaceae (2,3), which are ubiquitous in this area although the aecial stage has not been observed. To our knowledge, this is the first report of P. emaculata on switchgrass in Tennessee. Given the highly susceptible response of certain varieties of switchgrass to this rust in field plots, reduction in total biomass in large acreages is likely and long-standing fields of this perennial grass will compound the problem. References: (1) M. Gardes and T. D. Bruns. Mol. Ecol. 2:113, 1993. (2) D. M. Gustafson et al. Crop Sci. 43:755, 2003. (3) P. Ramachar and G. Cummins. Mycopathol. Mycol. Appl. 25:7, 1965. (4) R. Vilgalys and M. Hester. J. Bacteriol. 172:4238, 1990.
2007年春季,将柳枝稷品种阿拉莫(Alamo)、坎洛(Kanlow)、SL - 93 - 2001和NSL 2001 - 1(低地型)、布莱克韦尔(Blackwell)(高地型)以及格伦维尔(Grenville)、法尔肯(Falcon)和迈阿密(Miami)(倍性水平未知)播种于诺克斯维尔的东田纳西研究与推广中心,用于评估和进行受控杂交。2007年7月和8月,主要在柳枝稷品种阿拉莫、布莱克韦尔、格伦维尔、法尔肯、坎洛和迈阿密的叶片上表面观察到夏孢子堆,叶片下表面的夏孢子堆较少。2008年在所有品种和材料上均观察到了夏孢子堆。孢子尺寸报告为平均值±标准差。夏孢子堆生于叶上,正面,生于茎上,长圆形,肉桂褐色。夏孢子球形至宽椭圆形,26.0±3.0×23.2±2.4μm,壁肉桂褐色,厚1.5至2.0μm,具细刺,有三到四个赤道孔,与无斑柄锈菌(Puccinia emaculata Schw.)相符(3)。从格伦维尔、法尔肯和布莱克韦尔分离到大量冬孢子,从阿拉莫分离到的冬孢子较少。冬孢子堆生于叶上,正面,生于茎上,密集至散生排列,长圆形,深褐色至黑色。冬孢子深褐色,双细胞,椭圆形至长圆形,长33.6±4.8μm,顶细胞宽17.5±1.2μm,基细胞宽15.9±2.5μm。冬孢子壁侧面宽1.5至2.0μm,顶端宽4至6μm。柄褐色或无色,长达冬孢子的约一个长度,28.5±7.4μm。冬孢子形态证实该锈菌为无斑柄锈菌(3),据报道它可感染高地型和低地型柳枝稷群体(2)。对一个采自“法尔肯”的标本(GenBank登录号EU915294和BPI编号878722),用引物PRITS1F(L. A. Castlebury,未发表数据)和ITS4B(1)扩增一个片段、用引物Rust5.8SF(L. A. Castlebury,未发表数据)和LR7(4)扩增第二个片段,对包含大亚基核糖体DNA内部转录间隔区(ITS)1、5.8S、ITS 2和D1/D2区域的2109 bp片段进行测序。没有无斑柄锈菌的序列可用于比较;然而,对ITS进行BLAST搜索结果显示与天门冬柄锈菌(P. asparagi DC)(576条序列中的527条,91%)和红顶柄锈菌(P. andropogonis Schw.)(568条序列中的523条,92%)匹配,将该真菌归入柄锈菌属(Puccinia Pers.)。这种锈菌的转主寄主是大戟科植物(2,3),尽管未观察到锈菌的性孢子器阶段,但在该地区很常见。据我们所知,这是田纳西州关于柳枝稷上无斑柄锈菌的首次报道。鉴于某些柳枝稷品种在田间对这种锈菌高度敏感,大面积种植时总生物量可能会减少,而这种多年生草本植物的长期种植会使问题更加严重。参考文献:(1)M. Gardes和T. D. Bruns. Mol. Ecol. 2:113, 1993. (2)D. M. Gustafson等人. Crop Sci. 43:755, 2003. (3)P. Ramachar和G. Cummins. Mycopathol. Mycol. Appl. 25:7, 1965. (4)R. Vilgalys和M. Hester. J. Bacteriol. 172:4238, 1990.