源于广8 A杂交稻组合的稻瘟病菌无毒基因型分析
|
|
汪文娟,苏菁,杨健源,韦小燕,陈凯玲,陈珍,陈深,朱小源
|
Analysis of Magnaporthe oryzae Avirulent Genes in the Infected Hybrid Rice Combinations Derived from a Sterile Line of Guang 8 A
|
|
WANG WenJuan,SU Jing,YANG JianYuan,WEI XiaoYan,CHEN KaiLing,CHEN Zhen,CHEN Shen,ZHU XiaoYuan
|
|
表3 不同菌株对25个抗稻瘟单基因系的致病型
|
Table 3 Pathotypes of different strains against 25 blast-resistant lines
|
|
菌株
Strain | IRBLs单基因系对菌株的反应 Reactions of IRBLs to the strains |
LTH | | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 | 19 | 20 | 21 | 22 | 23 | 24 | 25 | | Pia | Pii | Piks | Pik | Pikp | Pikh | Piz | Piz5 | Pizt | Pita | Pib | Pit | Pish | Pi1 | Pi3 | Pi5 | Pi7 | Pi9 | Pi12 | Pi19 | Pikm | Pi20 | Pita2 | Pi11 | Pi50 | | GD12-535 | S | S | S | S | S | R | S | S | R | R | R | S | S | S | S | S | S | R | S | S | S | S | R | S | R | S | | GD13-3009 | S | R | S | R | R | R | R | R | S | S | R | R | R | S | R | R | R | R | S | S | R | S | S | S | R | S | | GD13-3024 | S | S | S | R | R | S | R | R | R | S | R | S | S | S | S | S | R | R | S | S | S | S | S | S | R | S | | GD13-493 | S | S | S | R | S | R | S | R | S | S | R | S | S | S | S | S | S | R | S | S | S | S | R | S | R | S | | GD13-621 | S | R | S | R | R | R | S | R | R | S | R | S | R | R | S | R | R | R | S | S | R | S | R | S | R | S | | GD13-659 | S | S | S | R | S | R | S | R | S | S | R | S | S | R | S | S | S | R | S | S | S | S | S | S | R | S | | GD14-070 | S | S | S | R | R | R | R | R | S | S | R | S | S | S | S | S | R | R | S | S | R | S | S | S | R | S | | GD14-349 | S | S | S | R | R | R | R | R | R | R | R | S | S | R | S | S | R | R | S | S | R | S | R | S | R | S | | GD14-366 | S | R | S | R | R | R | R | R | R | R | R | S | R | S | S | S | R | R | S | R | S | R | S | S | R | S | | GD14-368 | S | R | S | S | R | S | R | R | R | R | S | S | R | R | S | S | S | R | S | R | S | S | S | S | R | S | | GD14-376 | S | S | S | S | S | S | S | R | R | S | R | S | S | S | S | S | S | R | S | S | S | S | S | S | R | S | | GD14-401 | S | R | S | R | R | R | R | R | S | S | R | S | S | S | S | S | R | R | S | S | S | S | S | S | R | S | | GD15-23 | S | S | S | S | S | R | R | R | S | S | R | S | S | S | S | S | S | R | S | S | S | S | S | S | R | S | | GD15-259 | S | S | S | S | S | R | R | R | S | S | R | S | S | S | S | S | S | R | S | S | S | S | S | S | R | S | | GD15-270 | S | S | S | S | S | R | S | R | R | S | R | S | S | S | S | R | S | R | S | S | S | S | S | S | R | S | | GD15-291 | S | S | S | R | R | R | S | R | R | S | R | S | S | S | S | S | R | R | S | S | S | S | S | S | R | S | | GD15-315 | R | R | R | R | S | R | R | R | R | R | R | S | R | R | R | R | R | R | R | R | R | R | S | R | R | S | | GD15-436 | S | S | S | S | S | R | R | R | S | S | R | S | S | S | S | R | S | R | S | S | S | S | S | S | R | S | | GD15-506 | S | S | S | S | S | S | S | R | R | S | S | S | R | S | S | S | S | R | S | S | S | R | R | R | R | S | | GD15-523 | S | S | S | R | S | R | S | R | S | S | S | S | S | S | S | S | S | R | S | S | S | S | S | S | R | S | | GD15-530 | S | R | S | R | R | R | R | S | S | R | R | S | S | R | S | S | S | R | S | S | S | S | S | S | R | S | | GD15-586 | S | R | S | R | S | R | R | S | S | S | R | S | S | R | S | S | S | R | S | S | S | S | S | S | R | S | | GD16-272 | R | R | S | R | S | R | R | R | R | R | R | S | R | R | S | R | R | R | S | R | R | R | R | S | R | S | | GD16-280 | R | S | R | R | S | R | R | R | R | R | R | S | S | S | R | R | S | R | S | R | S | R | R | S | R | S | | GD16-3071 | S | S | S | S | S | R | S | R | R | S | R | S | S | S | S | S | S | R | S | S | S | R | R | R | R | S | | GD16-327 | S | S | S | R | S | R | S | R | S | S | S | S | S | R | S | R | S | R | S | S | S | S | S | S | R | S | | GD16-334 | S | S | S | S | S | R | R | R | S | S | R | S | S | S | S | S | S | R | S | S | S | S | S | S | R | S | 无毒基因频率
The frequency of
avirulent genes (%) | 11.1 | 33.3 | 7.4 | 63.0 | 37.0 | 85.2 | 59.3 | 88.9 | 51.9 | 29.6 | 85.2 | 3.7 | 25.9 | 33.3 | 11.1 | 29.6 | 37.0 | 100.0 | 3.7 | 18.5 | 22.2 | 22.2 | 29.6 | 11.1 | 100.0 | |
|
|
|