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Applied and Environmental Microbiology, June 1999, p. 2674-2678, Vol. 65, No. 6
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

PCR-Based Genotyping of Epidemic and Preepidemic Trichoderma Isolates Associated with Green Mold of Agaricus bisporus

X. Chen, C. P. Romaine,* Q. Tan,dagger B. Schlagnhaufer,Dagger M. D. Ospina-Giraldo, D. J. Royse, and D. R. Huff§

Department of Plant Pathology, The Pennsylvania State University, University Park, Pennsylvania 16802

Received 25 November 1998/Accepted 7 April 1999

We used randomly amplified polymorphic DNA (RAPD)-PCR to estimate genetic variation among isolates of Trichoderma associated with green mold on the cultivated mushroom Agaricus bisporus. Of 83 isolates examined, 66 were sampled during the recent green mold epidemic, while the remaining 17 isolates were collected just prior to the epidemic and date back to the 1950s. Trichoderma harzianum biotype 4 was identified by RAPD analysis as the cause of almost 90% of the epidemic-related episodes of green mold occurring in the major commercial mushroom-growing region in North America. Biotype 4 was more closely allied to T. harzianum biotype 2, the predominant pathogenic genotype in Europe, than to the less pathogenic biotype 1 and Trichoderma atroviride (formerly T. harzianum biotype 3). No variation in the RAPD patterns was observed among the isolates within biotype 2 or 4, suggesting that the two pathogenic biotypes were populations containing single clones. Considerable genetic variation, however, was noted among isolates of biotype 1 and T. atroviride from Europe. Biotype 4 was not represented by the preepidemic isolates of Trichoderma as determined by RAPD markers and PCR amplification of an arbitrary DNA sequence unique to the genomes of biotypes 2 and 4. Our findings suggest that the onset of the green mold epidemic in North America resulted from the recent introduction of a highly virulent genotype of the pathogen into cultivated mushrooms.


* Corresponding author. Mailing address: Department of Plant Pathology, 209 Buckhout Laboratory, The Pennsylvania State University, University Park, PA 16802. Phone: (814) 865-7132. Fax: (814) 863-7217. E-mail: cpr2{at}psu.edu.

dagger Present address: Edible Fungi Institute, Shanghai Academy of Agricultural Sciences, Shanghai 201006, People's Republic of China.

Dagger Present address: Pioneer Hi-Bred, Trait and Technology Development, Des Moines, IA 50131.

§ Present address: Department of Agronomy, The Pennsylvania State University, University Park, PA 16802.


Applied and Environmental Microbiology, June 1999, p. 2674-2678, Vol. 65, No. 6
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Rakeman, J. L., Bui, U., LaFe, K., Chen, Y.-C., Honeycutt, R. J., Cookson, B. T. (2005). Multilocus DNA Sequence Comparisons Rapidly Identify Pathogenic Molds. J. Clin. Microbiol. 43: 3324-3333 [Abstract] [Full Text]  
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