水稻苗期纹枯病抗性鉴定微室接种技术的改良

展开
  • 1浙江师范大学 化学与生命科学学院, 浙江 金华 321004
    2浙江省农业科学院, 病毒学与生物技术研究所, 杭州 310021
    3扬州大学 江苏省作物遗传生理重点实验室/教育部植物功能基因组学重点实验室,江苏 扬州 225009
    4湖南农业大学 湖南省作物种质创新与资源利用重点实验室,长沙 410128
*通讯联系人, E-mail:squ@mail.zaas.ac.cn

收稿日期: 2014-03-02

  修回日期: 2014-04-13

  网络出版日期: 2015-01-10

基金资助

转基因生物新品种培育重大专项(2012ZX08009001);浙江省农业科学院省部共建国家重点实验室培育基地开放基金资助项目(2010DS700124-KF1210)

Improvement of the Micro-chamber Inoculation Method for Determination of Rice Seedling Resistance to Sheath Blight (Rhizoctonia solani)

Expand
  • 1College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua 321004, China
    2Institute of Virology and Biotechnology, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China
    3Key Laboratory of Crop Genetics and Physiology of Jiangsu Province, College of Agriculture, Yangzhou University/Key Laboratory of Plant Functional Genomics of the Ministry of Education, Yangzhou 225009, China
    4Hunan Provincial Key Laboratory of Crop Germplasm Innovation and Utilization and College of Agronomy, Hunan Agricultural University, Changsha 410128, China
*Corresponding author, E-mail:squ@mail.zaas.ac.cn

Received date: 2014-03-02

  Revised date: 2014-04-13

  Online published: 2015-01-10

摘要

水稻对纹枯病的抗性属于典型的数量性状,多数栽培品种的抗病水平较低,并且抗性差异较小。水稻纹枯病接种和抗性评价体系是培育抗病品种的重要基础。利用植物生长箱的控温、控光和控湿条件以及生长势相对一致的水稻秧苗,对苗期纹枯病微室接种技术进行了改进。试验品种苗期的纹枯病抗性从高到低依次为YSBR1、特青、泰粳394、日本晴和Lemont,并且与大田成株期接种鉴定的结果一致。RT-PCR分析显示,苗期和成株期接种纹枯病菌均诱导4个水稻抗病相关基因的表达。通过“叶枕高”和“苗挺高”计算的各品种苗期病级变幅分别为2.82~8.54级和1.20~3.39级。前者与大田成株期的病级变幅一致,因而“叶枕高”病级计算方法更适用于微室接种鉴定体系。

本文引用格式

徐国娟, 袁正杰, 左示敏, 潘学彪, 王志龙, 瞿绍洪 . 水稻苗期纹枯病抗性鉴定微室接种技术的改良[J]. 中国水稻科学, 2015 , 29(1) : 97 -105 . DOI: 10.3969/j.issn.1001-7216.2015.01.012

Abstract

The sheath blight resistance in rice belongs to a typical quantitative trait, and most of the rice cultivars show low levels of resistance to the disease with small differences. The inoculation and scoring system for rice sheath blight is an important basis for breeding resistant rice cultivars. The micro-chamber method for determination of rice responses to the sheath blight pathogen Rhizoctonia solani was improved by inoculation to rice seedlings with similar growth vigour under controlled illumination, temperature and humidity conditions in a plant growth chamber. The rice cultivars YSBR1, Teqing, Taijing 394, Nipponbare and Lemont showed high to low levels of sheath blight resistance , which was consistent with the results of field inoculation in adult rice plants. RT-PCR analysis showed that the expression of four rice genes related to disease resistance was induced in inoculated seedlings and adult plants. Based on the height of the pulvinus of the second leaf from the top and the straightened seedling height the sheath blight scores ranged from 2.82 to 8.54 and from 1.20 to 3.39, respectively. The scoring method based on the height of the pulvinus led to similar disease scores for both seedlings and adult plants, and thus is more suitable for the micro-chamber inoculation system.

参考文献

[1] Lee F N, Rush M C.Rice sheath blight: A major rice disease.Plant Dis, 1983, 67(7): 829-832.
[2] Pan X B, Rush M C, Sha X Y, et al.Major gene, nonallelic sheath blight resistance from the rice cultivars Jasmine 85 and Teqing.Crop Sci, 1999, 39(2): 338-346.
[3] Zou J H, Pan X B, Chen Z X, et al.Mapping quantitative trait loci controlling sheath blight resistance in two rice cultivars(Oryza sativa L.). Theor Appl Genet, 2000, 101(4): 569-573.
[4] Jia Y L, Correa-Victoria F, McClung A, et al. Rapid determination of rice cultivar responses to the sheath blight pathogen Rhizoctonia solani using a micro-chamber screening method.Plant Dis, 2007, 91(5): 485-489.
[5] Savary S, Castilla N P, Elazegui F A, et al.Direct and indirect effects of nitrogen supply and disease source structure on rice sheath blight spread.Phytopathol, 1995, 85(9): 959-965.
[6] Lee F N, Moldenhauer K A K, Gibbons J W, et al. Rice blast and sheath blight evaluation results for the 2002 uniform regional rice nursery//Norman R J, Meullenet J F, Molden hayer K A K. Rice Research Studies. Fayetteville, AR: University of Arkansas Agriculture Experiment Station Research, 2002: 73-84.
[7] Sha X Y, Zhu L H.Resistance of some rice varieties to sheath blight (ShB).Int Rice Res Newsl, 1990, 15(6): 7-8.
[8] Li Z K, Pinson S R M, Marchetti M A, et al. Characterization of quantitative trait loci (QTLs) in cultivated rice contributing to field resistance to sheath blight (Rhizoctonia solani).Theor Appl Genet, 1995, 91(2): 382-388.
[9] Pinson S R M, Capdevielle F M, Oard J H. Confirming QTLs and finding additional loci conditioning sheath blight resistance in rice using recombinant inbred lines.Crop Sci, 2005, 45(2): 503-510.
[10] 左示敏,张亚芳,殷跃军,等. 田间水稻纹枯病抗性鉴定体系的确立与完善. 扬州大学学报:农业与生命科学版,2006,27(4):57-61.
[11] 左示敏,王子斌,陈夕军,等. 水稻纹枯病改良新抗源 YSBR1 的抗性评价. 作物学报,2009,35(4):608-614.
[12] Cartwright R D, Parsons P E, Sutton E A, et al.Disease monitoring and evaluation of rice cultivars on Arkansas farms//Norman R J, Meullenet J F, Molden hayer K A K. Rice Research Studies. Fayetteville, AR:University of Arkansas Agriculture Experiment Station Research, 2002: 219-228.
[13] 王子斌,左示敏,李刚,等. 水稻抗纹枯病苗期快速鉴定技术研究. 植物病理学报,2009,39(2):174-182.
[14] Jia Y L, Singh P, Eizenga G C, et al.In vitro identification of cultivar responses to rice sheath blight pathogen Rhizoctonia solani//Norman R J, Meullenet J F, Molden hayer K A K. Rice Research Studies. Fayetteville, AR:University of Arkansas Agriculture Experiment Station Research, 2002: 229-236.
[15] Prasad B, Eizenga G C.Rice sheath blight disease resistance identified in Oryza spp. accessions.Plant Dis, 2008, 92(11): 1503-1509.
[16] Jia L M, Yan W G, Zhu C S, et al.Allelic analysis of sheath blight resistance with association mapping in rice. PloS One, 2012, 7(3): e32703. (
[17] Liu G, Jia Y L, Correa-Victoria F J, et al. Mapping quantitative trait loci responsible for resistance to sheath blight in rice.Phytopathol, 2009, 99(9): 1078-1084.
[18] Yoshida S, Forno D A, Cock J H, et al.2nd edn.Laboratory Manual for physiological studies of rice. Los Bafios, Philippines:International Rice Research Institute, 1972: 57-63.
[19] 潘学彪,陈宗祥. 不同接种调查方法对抗水稻纹枯病遗传研究的影响. 江苏农学院学报,1997,18(3):27-32.
[20] 王子斌,左示敏,李刚,等. 水稻成株期对纹枯病的抗性表现研究. 吉林农业大学学报,2011,33(2):144-150.
[21] Singh G, Kumar S, Singh P.A quick method to isolate RNA from wheat and other carbohydrate-rich seeds.Plant Mol Biol Rep, 2003, 21(1): 93.
[22] Jain M, Nijhawan A, Tyagi A K, et al.Validation of housekeeping genes as internal control for studying gene expression in rice by quantitative real-time PCR.Biochem Biophys Res Commun, 2006, 345(2): 646-651.
[23] Magyar Z.Keeping the balance between proliferation and differentiation by the E2F transcriptional regulatory network is central to plant growth and development//Bögre L, Beemster G T S. Plant Growth Signaling. Springer-Verlag Berlin and Heidelberg GmbH & Co. K, 2008, 10: 89-105.
[24] Agrawal G K, Rakwal R, Jwa N S.Rice (Oryza sativa L.) OsPR1b gene is phytohormonally regulated in close interaction with light signals.Biochem Biophys Res Commun, 2000, 278(2): 290-298.
[25] Kim S G, Kim S T, Wang Y M, et al.The RNase activity of rice probenazole-induced protein1 (PBZ1) plays a key role in cell death in plants.Mol Cells, 2011, 31(1): 25-31.
[26] Crouzet J, Trombik T, Fraysse Å S, et al.Organization and function of the plant pleiotropic drug resistance ABC transporter family.FEBS lett, 2006, 580(4): 1123-1130.
[27] Rush M C, Hoff B J, Mellrath W O.A uniform disease rating system for rice disease in the United States. Proc 16th Rice Tech Working Group, Lake Charles, Louisana, USA, 1976: 64.
[28] Eizenga G C, Lee F N, Rutger J N.Screening Oryza species plants for rice sheath blight resistance.Plant Dis, 2002, 86(7): 808-812.
[29] Wasano K, Oro S, Kido Y.The syringe inoculation method for selecting rice plants resistant to sheath blight, Rhizoctonia solani Kühn.Japan J Trop Agric, 1983, 27(3): 131-134.
文章导航

/

浙ICP备05004719号-5
公安备案号:33010302003356
地址:浙江省杭州市富阳区水稻所路28号 邮编:311400 电话:0571-63370278 E-mail:cjrs@263.net
本系统由北京玛格泰克科技发展有限公司设计开发
总访问量: 今日访问: 在线人数: