Sharma P, Sharma I, Bhardwaj S C
Directorate of Wheat Research, Karnal, Haryana, 132 001 India.
Regional Station, Directorate of Wheat Research, Flowerdale, Shimla-171 002, Himachal Pradesh, India.
Plant Dis. 2012 Oct;96(10):1580. doi: 10.1094/PDIS-05-12-0434-PDN.
Annual surveys of pathogen populations have monitored the changing pathotype situation of Puccinia triticina that causes leaf (brown) rust of wheat, to release and deploy rust-resistant cultivars of wheat in India. In surveys during 2009 to 2010, samples of leaf rust infecting wheat were collected from the Solan district of Himachal Pradesh. The samples were established on susceptible wheat cv. Agra Local and pathotypes were identified on three differentials following binomial nomenclature (3). Based on the infection types on sets of differentials, this sample was found different to all the known pathotypes of P. triticina from India. This report records a new pathotype of race group 104 of P. triticina from India. Unique feature of this pathotype is its avirulence to Lr3 (Democrat) and virulence to Lr10, Lr13, Lr23, Lr26. These genes are the most common resistance genes in Indian wheat material (1). It appears to be a result of reverse mutation on Lr3 in pathotype 21R63 (104-3). In 2012, this pathotype was detected in 5% of samples from northern India. The new pathotype produces susceptible infection type on Lr10 to which 104 groups gives mesothetic response (4). When compared to other pathotypes of the 104 group, it was different to pathotype 29R23 (104B) in avirulence to Lr26, to which pathotype 93R57 (104-4) is virulent. All the other pathotypes of the 104 group are virulent to Lr3, to which new pathotypes are avirulent. The new pathotype produces resistant response on Lr2a, Lr3, Lr9, Lr15, Lr19, Lr24, Lr25, Lr28, Lr32, Lr39, Lr45, Lr47, and susceptible response on Lr1, Lr2b, Lr2c, Lr10, Lr11, Lr12, Lr13, Lr14a, Lr14b, Lr14ab, Lr16, Lr17a, Lr17b, Lr18, Lr20, Lr21, Lr22a, Lr22b, Lr23, Lr26, Lr27+31, Lr29, Lr30, Lr33, Lr34, Lr35, Lr36, Lr37, Lr38, Lr40, Lr44, Lr46, Lr48, Lr49, Lr51, and Lr57. It is designated as NHKSP on international differentials. A live culture is being maintained as well as cryo-preserved in the National Repository of Pathotypes at the Regional Station of Directorate of Wheat Research, Shimla. Initial evaluation of 700 Indian and exotic wheat lines revealed that more than 500 lines possesses resistance to this pathotype. The identity of the pathotype was also confirmed by sequencing the internal transcribed spacer region of the rDNA with the primers ITS1/ITS4 (GenBank Accession No. JX020949) (2). Analysis of rDNA sequence identified this pathotype as a variant of P. triticina. The strain was most similar to ANK9538 of P. triticina (Accession No. DQ 147418, 98%) and 77-5 strain of P. triticina (Accession No. JQ360856, 93%). Identification of pathotypes from wheat growing areas in the initial stages is a prime effort that helps in developing ecologically safe, economic, and effective ways to manage wheat rusts. References: (1) S. C. Bhardwaj et al. Indian Phytopathol. 63:174, 2010. (2) M. A. Innis et al. PCR Protocols: A Guide to Methods and Applications. Academic Press. San Diego, CA, 1990. (3) S. Nagarajan et al. Curr. Sci. 52:413, 1983. (4) S. K. Nayar et al. Indian Phytopathol. 51:290, 1998.
对病原菌种群的年度调查监测了引起小麦叶(条)锈病的小麦条锈菌致病型的变化情况,以便在印度选育和推广抗锈小麦品种。在2009年至2010年的调查中,从小麦叶锈病感染样本中采集了来自喜马偕尔邦索兰地区的样本。这些样本接种在感病小麦品种“阿格拉本地种”上,并按照二项式命名法在三个鉴别品种上鉴定致病型(3)。根据在鉴别品种上的侵染类型,发现该样本与印度所有已知的小麦条锈菌致病型均不同。本报告记录了来自印度的小麦条锈菌第104小种的一个新致病型。该致病型的独特之处在于它对Lr3(民主党)无毒,而对Lr10、Lr13、Lr23、Lr26有毒。这些基因是印度小麦材料中最常见的抗性基因(1)。它似乎是致病型21R63(104 - 3)中Lr3发生反向突变的结果。2012年,在印度北部5%的样本中检测到了这种致病型。这种新致病型在Lr10上产生感病侵染类型,而第104小种的其他类型对此产生中间型反应(4)。与第104小种的其他致病型相比,它在对Lr26无毒方面与致病型29R23(104B)不同,而致病型93R57(104 - 4)对Lr26有毒。第104小种的所有其他致病型对Lr3有毒,而新致病型对Lr3无毒。这种新致病型在Lr2a、Lr3、Lr9、Lr15、Lr19、Lr24、Lr25、Lr28、Lr32、Lr39、Lr45、Lr47上产生抗性反应,在Lr1、Lr2b、Lr2c、Lr10、Lr11、Lr12、Lr13、Lr14a、Lr14b、Lr14ab、Lr16、Lr17a、Lr17b、Lr18、Lr20、Lr21、Lr22a、Lr22b、Lr23、Lr26、Lr27 + 31、Lr29、Lr30、Lr33、Lr34、Lr35、Lr36、Lr37、Lr38、Lr40、Lr44、Lr46、Lr48、Lr49、Lr51和Lr57上产生感病反应。在国际鉴别品种上它被指定为NHKSP。一种活体培养物正在位于西姆拉的小麦研究局区域站的国家致病型保存库中保存以及超低温保存。对700个印度和外来小麦品系的初步评估表明,超过500个品系对这种致病型具有抗性。通过使用引物ITSl/ITS4对rDNA的内部转录间隔区进行测序(GenBank登录号JX020949)(2)也证实了该致病型的身份。rDNA序列分析确定这种致病型是小麦条锈菌的一个变种。该菌株与小麦条锈菌的ANK9538(登录号DQ 147418,相似度98%)和小麦条锈菌的77 - 5菌株(登录号JQ360856,相似度93%)最为相似。在初始阶段从小麦种植区鉴定致病型是一项重要工作,有助于开发生态安全、经济且有效的方法来防治小麦锈病。参考文献:(1)S. C. Bhardwaj等人,《印度植物病理学》63:174,2010年。(2)M. A. Innis等人,《PCR实验方案:方法与应用指南》,学术出版社,加利福尼亚州圣地亚哥,1990年。(3)S. Nagarajan等人,《当代科学》52:413,1983年。(4)S. K. Nayar等人,《印度植物病理学》51:290,1998年。