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由小麦秆锈菌小麦专化型引起的秆锈病在东非小麦上的传播,该菌对Sr31具有毒性

The Spread of Stem Rust Caused by Puccinia graminis f. sp. tritici, with Virulence on Sr31 in Wheat in Eastern Africa.

作者信息

Wanyera R, Kinyua M G, Jin Y, Singh R P

机构信息

Kenya Agricultural Research Institute, National Plant Breeding Research Center, P.O. Njoro, Kenya.

USDA-ARS Cereal Disease Laboratory, University of Minnesota, St. Paul.

出版信息

Plant Dis. 2006 Jan;90(1):113. doi: 10.1094/PD-90-0113A.

Abstract

Stem rust resistance in wheat cultivars with Sr31 has been effective and durable worldwide for more than 30 years. Isolates of Puccinia graminis f. sp. tritici with virulence to Sr31 were detected in Uganda in 1999 (1). During 2003 and 2004, a majority of current Kenyan cultivars and a large portion of CIMMYT wheat germplasm with gene Sr31 planted in Kenya were susceptible to stem rust. Six isolates collected during 2004 at different locations in Kenya were tested for virulence on the 16 North American stem rust race differentials with the following Sr genes: Sr5, 6, 7b, 8a, 9a, 9b, 9d, 9e, 9g, 10, 11, 17, 21, 30, 36, and Tmp. An extended set of designated Sr genes (Sr13, 19, 22, 24, 25, 26, 29, 31, 32, 33, 35, 37, 39, 40, 44, and Wld-1) was also tested at the seedling stage. An isolate from Uganda collected in 1999 with virulence on Sr31 was used for comparison. Urediniospores suspended in a lightweight mineral oil were inoculated onto 7-day-old seedlings. Inoculated plants were placed in a dew chamber for 14 h at 18°C in the dark and then for an additional period of 3 to 4 h placed under fluorescent light. Plants were incubated in a greenhouse at 18 ± 2°C with a photoperiod of 16 h. Infection types (IT), described by Stakman et al. (3), were assessed after 14 days postinoculation. All isolates from Kenya exhibited a low infection type (IT 0) on line W2691SrTt-1 (donor of Sr36), a low infection type (IT 2) on cv. Triumph 64 (donor of SrTmp), and high infection types (IT 3 or 4) on all other lines in the differential set (2); thus these isolates were keyed to race TTKS. The virulence pattern of the isolate collected in 1999 from Uganda was identical to that from Kenya on the differential set and on the extended set of designated Sr genes. In this study, these isolates produced a high infection type (IT 3) on Einkorn and CnSSr21Tm (a derivative of Triticum monococcum in Chinese Spring background), two sources of Sr21 used in our study, whereas the isolate with Sr31-virulence from Uganda in 1999 was reported to be avirulent on Sr21 (1). These isolates produced high infection types on single gene lines with Sr31 and winter wheat cvs. Custer, Foster, GA-Dozier, Patton, and Pioneer 26R61, which were known to carry the 1BL.1RS translocation with Sr31. These isolates were also virulent on SrWld-1, a gene used in spring wheat for its resistance to North American stem rust isolates. In addition to Sr36 and SrTmp, other stem rust resistance genes that were effective against TTKS at the seedling stage include Sr13, 22, 24, 25, 26, 27, 29, 32, 33, 35, 37, 39, 40, and 44. Cultivars, breeding germplasm, and single gene lines are currently being evaluated for adult plant reaction in Kenya. Results from this study indicated that stem rust isolates with virulence on Sr31 are now wide spread in the Eastern Africa highlands and pose a threat to wheat production in the region, as well as in other wheat production areas where Sr31 resistance is important. A rapid deployment of effective resistance genes to this race in breeding programs throughout Eastern Africa and Asia is needed to reduce this threat. References: (1) Z. A. Pretorius et al. Plant Dis. 84:203, 2000. (2) A. P. Roelfs and J. W. Martens. Phytopathology 78:526, 1988. (3) E. C. Stakman et al. U.S. Department of Agriculture. ARS E-617, 1962.

摘要

携带Sr31的小麦品种的秆锈病抗性在全球范围内已有效且持久地保持了30多年。1999年在乌干达检测到对Sr31具有毒性的小麦秆锈菌(Puccinia graminis f. sp. tritici)分离株(1)。在2003年和2004年期间,肯尼亚目前的大多数品种以及种植在肯尼亚的大部分携带Sr31基因的国际玉米小麦改良中心(CIMMYT)小麦种质对秆锈病敏感。对2004年在肯尼亚不同地点收集的6个分离株进行了测试,检测其对16个北美秆锈病生理小种鉴别寄主的毒性,这些鉴别寄主带有以下Sr基因:Sr5、6、7b、8a、9a、9b、9d、9e、9g、10、11、17、21、30、36和Tmp。还在幼苗期对一组扩展的指定Sr基因(Sr13、19、22、24、25、26、29、31、32、33、35、37、39、40、44和Wld - 1)进行了测试。将1999年从乌干达收集的对Sr31具有毒性的一个分离株用作对照。将悬浮在轻质矿物油中的夏孢子接种到7日龄的幼苗上。接种后的植株在黑暗中于18°C的保湿箱中放置14小时,然后在荧光灯下再放置3至4小时。植株在18±2°C、光周期为16小时的温室中培养。接种后14天评估由斯塔克曼等人(3)描述的侵染类型(IT)。来自肯尼亚的所有分离株在W2691SrTt - 1品系(Sr36的供体)上表现出低侵染类型(IT 0),在品种Triumph 64(SrTmp的供体)上表现出低侵染类型(IT 2),而在鉴别寄主组中的所有其他品系上表现出高侵染类型(IT 3或4)(2);因此,这些分离株被鉴定为生理小种TTKS。1999年从乌干达收集的分离株在鉴别寄主组和扩展的指定Sr基因组上的毒性模式与来自肯尼亚的分离株相同。在本研究中,这些分离株在一粒小麦以及CnSSr21Tm(中国春背景下一粒小麦的衍生物)上产生了高侵染类型(IT 3),这是我们研究中使用的Sr21的两个来源;而1999年来自乌干达的对Sr31具有毒性的分离株据报道对Sr21无毒性(1)。这些分离株在带有Sr31的单基因品系以及冬小麦品种Custer、Foster、GA - Dozier、Patton和Pioneer 26R61上产生了高侵染类型,这些品种已知携带带有Sr31的1BL.1RS易位。这些分离株对SrWld - 1也具有毒性,SrWld - 1是春小麦中用于抵抗北美秆锈菌分离株的一个基因。除了Sr36和SrTmp之外,在幼苗期对TTKS有效的其他秆锈病抗性基因包括Sr13、22、24、25、26、27、29、32、

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