Use of Polymerase Chain Reaction To Detect the Take-All Fungus, Gaeumannomyces graminis , in Infected Wheat Plants

Author:

Schesser Kurt1,Luder Andreas1,Henson Joan M.1

Affiliation:

1. Department of Microbiology, Montana State University, Bozeman, Montana 59717

Abstract

Gaeumannomyces graminis , the causative agent of take-all disease of wheat, barley, and oats, was detected in infected wheat seedlings by using the polymerase chain reaction to amplify Gaeumannomyces -specific DNA fragments. Nested primers and two rounds of amplification were used to amplify two fragments, approximately 287 and 188 bp in size, from G. graminis -infected wheat seedlings. The use of nested primers greatly decreased the number of nonspecific amplification products. Polymerase chain reaction products were not obtained with DNA from seedlings infected with several other phytopathogenic fungi or with DNA from uninfected seedlings. Amplified products were visualized on agarose gels, and their identities were confirmed by DNA hybridization. This method did not require culturing the fungus and has potential for detecting G. graminis in infested wheat, barley, or oat fields.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference26 articles.

1. A rapid alkaline extraction procedure for screening recombinant plasmid DNA;Birnboim H. C.;Nucleic Acids Res.,1979

2. Nuclear distribution in vegetative cells of Ophiobolus graminis and other cereal root pathogens;Chambers S. C.;Aust. J. Biol. Sci.,1970

3. One-step preparation of competent Escherichia coli: transformation and storage of bacterial cells in the same solution;Chung C. T.;Proc. Natl. Acad. Sci. USA,1989

4. Clarkson J. D. S. and R. W. Polley. 1981. Diagnosis assessment crop-loss appraisal and forecasting p. 251-269. In M. J. C. Asher and P. J. Shipton (ed.) Biology and control of take-all. Academic Press Inc. (London) Ltd. London.

5. A cofnprehensive set of sequence analysis programs for the VAX;Devereux J.;Nucleic Acids Res.,1984

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3