Jain S K, Prashar M, Bhardwaj S C, Singh S B, Sharma Y P
Regional Station, Directorate of Wheat Research (ICAR), Flowerdale, Shimla-171 002, Himachal Pradesh, India.
Plant Dis. 2009 Aug;93(8):840. doi: 10.1094/PDIS-93-8-0840B.
Stem (black) rust, caused by Puccinia graminis Pers. f. sp. tritici Eriks. & Henn., is one of the most destructive diseases of wheat. It could be controlled through introgression of race-specific resistance genes. However, such kind of resistance is mostly short lived due to emergence of new virulences. For example, resistance genes Sr11, Sr24, Sr30, and Sr31 are no longer effective (2,4). Detection of new virulences has remained vital in the evaluation and identification of new sources of resistance. We report here the detection of virulence to Sr25, a gene from Thinopyrum elongatum (4), which had been effective or partially effective against stem rust worldwide, including race Ug99 (TTKSK) (4). A stem rust isolate collected in 2006 from Karnataka (southern India) produced susceptible reactions (infection type [IT] 3+ to 4) on the primary leaves of differential genotype 'Agatha' carrying Sr25 and susceptible check 'Agra Local' at 22 ± 2°C. To verify virulence to Sr25, single-pustule isolates from this sample were inoculated onto seedlings of 'Agrus', 'Agatha', 'RL6040' ('Thatcher' + Sr25), 'Superseri#1', 'Wheatear', and 'Morocco' + Sr25 (obtained from CIMMYT), which all carry Sr25. All these accessions were found susceptible (IT 3+ to 4) to this isolate, except Wheatear which expressed resistance (IT ;1), indicating the presence of additional gene(s). These genotypes are resistant (ITs ;1 to 2+) to Sr25-avirulent pathotypes. The new pathotype is avirulent to Sr11, 13, 14, 21, 22, 23, 24, 26, 27, 29, 31, 32, 33, 35, 37, 38, 39, 40, 43, and Tmp and virulent to Sr5, 6, 7a, 7b, 8a, 9a, 9b, 9d, 9e, 9f, 9g, 10, 12, 15, 16, 17, 18, 19, 20, 25, 28, 30, 34, 36, 42, Wld-1, and Gt at 22 ± 2°C. This pathotype has been designated as 58G13-3 and PKTSC according to the Indian nomenclature (1) and the North American system (3), respectively. It represents race 40 based on Stakman's differentials. It may have arisen from race 40 through mutation. The type culture of the pathotype has been added to the culture collection at Flowerdale, Shimla. Interestingly, 'Festiguay' (Sr30) was found resistant to this pathotype, indicating the presence of additional gene(s), whereas 'Webster' (Sr30) was susceptible. Adult plants of Agrus, Agatha, RL6040, Superseri#1, and Morocco+Sr25 also were susceptible, producing 20S to 60S responses. Sr25-avirulent pathotype 62G29 produced a TR (flecking in traces) response on these lines except Morocco + Sr25 that showed 20 to 40MR (moderately resistant) responses. In the same study however, adult plants of Thatcher showed a resistant reaction (10R to MR) at low (16 ± 2°C) and susceptible (20S) at high (22 ± 2°C) temperatures. Agatha and RL6040, having Thatcher as one of the parents, had similar responses. The detection of Sr25 virulence is significant since Sr25 is an important gene to be targeted for breeding wheat cultivars resistant to Ug99. We should use either adult plant resistance and/or pyramiding two or more genes for seedling resistance to enhance the field life of wheat cultivars. References: (1) P. Bahadur et al. Proc. Indian Acad. Sci. 95:29, 1985. (2) S. C. Bhardwaj et al. J. Wheat Res. 1:51, 2007. (3) Y. Jin et al. Plant Dis. 92:923, 2008. (4) R. P. Singh et al. CAB Rev. No. 054:1, 2006.
由禾柄锈菌小麦专化型(Puccinia graminis Pers. f. sp. tritici Eriks. & Henn.)引起的秆(条)锈病是小麦最具毁灭性的病害之一。可以通过导入小种专化抗性基因来控制该病。然而,由于新毒性的出现,这种抗性大多寿命短暂。例如,抗性基因Sr11、Sr24、Sr30和Sr31已不再有效(2,4)。在评估和鉴定新的抗性来源时,检测新毒性仍然至关重要。我们在此报告对Sr25的毒性检测,Sr25是来自长穗偃麦草(Thinopyrum elongatum)的一个基因(4),该基因在全球范围内对秆锈病一直有效或部分有效,包括对小种Ug99(TTKSK)(4)。2006年从印度南部卡纳塔克邦采集的一个秆锈菌分离株,在22±2°C条件下,在携带Sr25的鉴别基因型‘Agatha’的初生叶以及感病对照‘Agra Local’上产生感病反应(侵染型[IT] 3+至4)。为了验证对Sr25的毒性,将该样本的单疱分离株接种到‘Agrus’、‘Agatha’、‘RL6040’(‘Thatcher’+Sr25)、‘Superseri#1’、‘Wheatear’和‘Morocco’+Sr25(从国际玉米小麦改良中心获得)的幼苗上,这些材料均携带Sr25。除了表现出抗性(IT;1)的‘Wheatear’外,所有这些材料对该分离株均感病(IT 3+至4),这表明存在其他基因。这些基因型对Sr25无毒力致病型具有抗性(ITs;1至2+)。这种新的致病型对Sr11、13、14、21、22、23、24、26、27、29、31、32、33、35、37、38、39、40、43和Tmp无毒,在22±2°C条件下对Sr5、6、7a、7b、8a、9a、9b、9d、9e、9f、9g、10、12、15、16、17、18、19、20、25、28、30、34、36、42、Wld - 1和Gt有毒。根据印度命名法(1)和北美系统(3),这种致病型分别被指定为58G13 - 3和PKTSC。根据斯塔克曼鉴别体系,它代表小种40。它可能是由小种40通过突变产生的。该致病型的模式培养物已被添加到西姆拉弗劳戴尔的培养物保藏中心。有趣的是,‘Festiguay’(Sr30)对这种致病型表现出抗性,表明存在其他基因,而‘Webster’(Sr30)感病。‘Agrus’、‘Agatha’、‘RL6040’、‘Superseri#1’和‘Morocco’+Sr25的成株也感病,产生20S至60S的反应。Sr25无毒力致病型62G29在这些品系上产生TR(微量病斑)反应,除了‘Morocco’+Sr25表现出20至40MR(中度抗性)反应。然而,在同一研究中,‘Thatcher’的成株在低温(16±2°C)下表现出抗性反应(10R至MR),在高温(