DGGE AS A SENSITIVE METHOD TO DETECT SHIFTS IN MICROBIAL POPULATIONS DURING A LONG-TERM FIELD STUDY

Authors: VIEBAHN, M - UTRECHT UNIV; OUWENS, T.W.M. - UTRECHT UNIV; GLANDORF, D.C.M. - NAT.INST.HEALTH & ENVIRO.; SMIT, E - NAT.INST.HEALTH & ENVIRO.; LEEFLANG, P - NAT.INST.HEALTH & ENVIRO.; WERNARS, K - NAT.INST.HEALTH & ENVIRO.; Thomashow, Linda; VAN LOON, L - UTRECHT UNIV; BAKKER, P.A.H.M - UTRECHT UNIV

Submitted to: International Congress of Plant Pathology Abstracts and Proceedings
Publication Type: Other
Publication Acceptance Date: 1/20/2003
Publication Date: 2/20/2003
Citation: Viebahn, M., Ouwens, T., Glandorf, D., Smit, E., Leeflang, P., Wernars, K., Thomashow, L.S., Van Loon, L.C., Bakker, P. Dgge as a sensitive method to detect shifts in microbial populations during a long-term field study. International Congress of Plant Pathology Abstracts and Proceedings.2003. Vol. 2.,pg 172.

Interpretive Summary:

Technical Abstract: Pseudomonas putida WCS358r, genetically modified to have improved activity against soil-borne pathogens, was released into the rhizosphere of wheat. Two genetically modified derivatives carried the phz or the phl biosynthetic gene loci and constitutively produced either the antifungal compound phenazine-1-carboxylic acid (PCA) or the antifungal and antibacterial compound 2,4-diacetylphloroglucinol (DAPG). In 1997 and 1998, effects of single introductions of PCA producing derivatives on the indigenous microflora were studied. A transient shift in the composition of the total fungal microflora, determined by amplified ribosomal DNA restiction analysis (ARDRA), was detected. Starting in 1999, effects of repeated introduction of genetically modified microorganisms (GMMs) were studied. Wheat seeds coated with the PCA producer, the DAPG producer, a mixture of the PCA and DAPG producers, or WCS358r, were sown and the densities, composition and activities of the rhizosphere microbial populations were measured. All introduced strains decreased from 10(7)CFU per gram of rhizosphere sample to below the detection limit after harvest of the wheat plants. The phz genes were stably maintained in the PCA producers, and PCA was detected in rhizosphere extracts of plants treated with this strain or with the mixture of the PCA and DAPG producers. The phl genes were also stably maintained in the DAPG producing derivative of WCS358r. Effects of the genetically modified bacteria on the rhizosphere fungi and bacteria were analyzed by using amplified ribosomal DNA restriction analysis. Introduction of the genetically modified bacterial strains caused a transient change in the composition of the rhizosphere microflora. However, introduction of the GMMs did not affect the several soil microbial activities that were investigated in this study.