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Applied and Environmental Microbiology, August 2001, p. 3371-3378, Vol. 67, No. 8
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.8.3371-3378.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Effect of Genetically Modified Pseudomonas putida WCS358r on the Fungal Rhizosphere Microflora of Field-Grown Wheat

Debora C. M. Glandorf,1,dagger Patrick Verheggen,1 Timo Jansen,1 Jan-Willem Jorritsma,1 Eric Smit,2 Paula Leeflang,2 Karel Wernars,2 Linda S. Thomashow,3 Eric Laureijs,4 Jane E. Thomas-Oates,4,Dagger Peter A. H. M. Bakker,1,* and Leendert C. van Loon1

Section of Phytopathology, Institute of Biology,1 and Department of Mass Spectrometry, Faculty of Chemistry,4 Utrecht University, Utrecht, and National Institute of Public Health and the Environment, Bilthoven,2 The Netherlands, and USDA-ARS, Washington State University, Pullman, Washington3

Received 9 January 2001/Accepted 15 May 2001

We released genetically modified Pseudomonas putida WCS358r into the rhizospheres of wheat plants. The two genetically modified derivatives, genetically modified microorganism (GMM) 2 and GMM 8, carried the phz biosynthetic gene locus of strain P. fluorescens 2-79 and constitutively produced the antifungal compound phenazine-1-carboxylic acid (PCA). In the springs of 1997 and 1998 we sowed wheat seeds treated with either GMM 2, GMM 8, or WCS358r (approximately 107 CFU per seed), and measured the numbers, composition, and activities of the rhizosphere microbial populations. During both growing seasons, all three bacterial strains decreased from 107 CFU per g of rhizosphere sample to below the limit of detection (102 CFU per g) 1 month after harvest of the wheat plants. The phz genes were stably maintained, and PCA was detected in rhizosphere extracts of GMM-treated plants. In 1997, but not in 1998, fungal numbers in the rhizosphere, quantified on 2% malt extract agar (total filamentous fungi) and on Komada's medium (mainly Fusarium spp.), were transiently suppressed in GMM 8-treated plants. We also analyzed the effects of the GMMs on the rhizosphere fungi by using amplified ribosomal DNA restriction analysis. Introduction of any of the three bacterial strains transiently changed the composition of the rhizosphere fungal microflora. However, in both 1997 and 1998, GMM-induced effects were distinct from those of WCS358r and lasted for 40 days in 1997 and for 89 days after sowing in 1998, whereas effects induced by WCS358r were detectable for 12 (1997) or 40 (1998) days. None of the strains affected the metabolic activity of the soil microbial population (substrate-induced respiration), soil nitrification potential, cellulose decomposition, plant height, or plant yield. The results indicate that application of GMMs engineered to have improved antifungal activity can exert nontarget effects on the natural fungal microflora.


* Corresponding author. Mailing address: Utrecht University, Institute of Biology, Section of Phytopathology, P.O. Box 80084, 3508 TB Utrecht, The Netherlands. Phone: 31 30 2536861. Fax: 31 30 2518366. E-mail: P.A.H.M.Bakker{at}bio.uu.nl.

dagger Present address: National Institute of Health and the Environment, Bilthoven, The Netherlands.

Dagger Present address: Michael Barber Center for Mass Spectrometry, UMIST, Manchester, United Kingdom.


Applied and Environmental Microbiology, August 2001, p. 3371-3378, Vol. 67, No. 8
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.8.3371-3378.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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