Wang Baotong, Hu Xiaoping, Li Qiang, Hao Baojun, Zhang Bo, Li Gaobao, Kang Zhensheng
College of Plant Protection and Shaanxi Key Laboratory of Molecular Biology for Agriculture, Northwest A&F University, Yangling, 712100, China.
Plant Dis. 2010 Feb;94(2):221-228. doi: 10.1094/PDIS-94-2-0221.
Wheat stripe rust, caused by Puccinia striiformis f. sp. tritici, is a devastating disease in China. Races CYR32 and CYR33 have been predominant in the recent P. striiformis f. sp. tritici population. To develop molecular markers for these races, initially 86 isolates, most of which were collected in 2007 throughout China, were tested on the set of wheat genotypes for differentiating Chinese P. striiformis f. sp. tritici races, and their genomic DNA were amplified with 94 random amplified polymorphic DNA (RAPD) primers. Twelve isolates were identified as CYR33, 14 as CYR32, and 60 as 13 other races. A 320-bp band was identified to be associated with CYR32 with primer S1271 (5'-CTTCTCGGTC-3'), and a 550-bp band was identified to be specific to CYR33 with primer S1304 (5'-AGGAGCGACA-3'). The two bands were cloned and sequenced. Based on the sequences, sequence characterized amplified region (SCAR) markers CYR32sp1/sp2 and CYR33sp1/sp2 were developed to differentiate CYR32 and CYR33, respectively, from other races. The SCAR markers were validated with DNA samples from wheat leaves inoculated with selected isolates from the 86 isolates and urediniospore DNA samples from an additional 63 isolates collected from 2006 to 2009. The detection of CYR32 and CYR33 with the SCAR markers was completely consistent with the results of the race identification with the set of differential wheat genotypes. Thus, the markers are highly reliable for identification of the two races.
由条形柄锈菌小麦专化型(Puccinia striiformis f. sp. tritici)引起的小麦条锈病是中国一种极具毁灭性的病害。CYR32和CYR33小种在最近的条形柄锈菌小麦专化型群体中占主导地位。为开发针对这些小种的分子标记,最初对86个分离株进行了测试,其中大部分是2007年在中国各地收集的,利用一套用于区分中国条形柄锈菌小麦专化型小种的小麦基因型进行测试,并使用94条随机扩增多态性DNA(RAPD)引物对其基因组DNA进行扩增。12个分离株被鉴定为CYR33,14个为CYR32,60个为其他13个小种。使用引物S1271(5'-CTTCTCGGTC-3')鉴定出一条320 bp的条带与CYR32相关,使用引物S1304(5'-AGGAGCGACA-3')鉴定出一条550 bp的条带是CYR33特有的。这两条条带被克隆并测序。基于这些序列,开发了序列特征性扩增区域(SCAR)标记CYR32sp1/sp2和CYR33sp1/sp2,分别用于将CYR32和CYR33与其他小种区分开来。利用从86个分离株中挑选的分离株接种小麦叶片的DNA样本以及从2006年至2009年收集的另外63个分离株的夏孢子DNA样本对SCAR标记进行了验证。用SCAR标记检测CYR32和CYR33的结果与用一套鉴别小麦基因型进行小种鉴定的结果完全一致。因此,这些标记对于鉴定这两个小种高度可靠。