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Applied and Environmental Microbiology, April 1999, p. 1428-1434, Vol. 65, No. 4
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Suppression of the Biocontrol Agent Trichoderma harzianum by Mycelium of the Arbuscular Mycorrhizal Fungus Glomus intraradices in Root-Free Soil

Helge Green,1,* John Larsen,2,dagger Pål Axel Olsson,3 Dan Funck Jensen,1 and Iver Jakobsen2

Plant Pathology Section, Department of Plant Biology, The Royal Veterinary and Agricultural University, DK-1871 Frederiksberg C,1 and Plant Biology and Biogeochemistry Department, Risø National Laboratory, DK-4000 Roskilde,2 Denmark; and Department of Microbial Ecology, Lund University, S-223 62 Lund, Sweden3

Received 27 July 1998/Accepted 7 January 1999

Trichoderma harzianum is an effective biocontrol agent against several fungal soilborne plant pathogens. However, possible adverse effects of this fungus on arbuscular mycorrhizal fungi might be a drawback in its use in plant protection. The objective of the present work was to examine the interaction between Glomus intraradices and T. harzianum in soil. The use of a compartmented growth system with root-free soil compartments enabled us to study fungal interactions without the interfering effects of roots. Growth of the fungi was monitored by measuring hyphal length and population densities, while specific fatty acid signatures were used as indicators of living fungal biomass. Hyphal 33P transport and beta -glucuronidase (GUS) activity were used to monitor activity of G. intraradices and a GUS-transformed strain of T. harzianum, respectively. As growth and metabolism of T. harzianum are requirements for antagonism, the impact of wheat bran, added as an organic nutrient source for T. harzianum, was investigated. The presence of T. harzianum in root-free soil reduced root colonization by G. intraradices. The external hyphal length density of G. intraradices was reduced by the presence of T. harzianum in combination with wheat bran, but the living hyphal biomass, measured as the content of a membrane fatty acid, was not reduced. Hyphal 33P transport by G. intraradices also was not affected by T. harzianum. This suggests that T. harzianum exploited the dead mycelium but not the living biomass of G. intraradices. The presence of external mycelium of G. intraradices suppressed T. harzianum population development and GUS activity. Stimulation of the hyphal biomass of G. intraradices by organic amendment suggests that nutrient competition is a likely means of interaction. In conclusion, it seemed that growth of and phosphorus uptake by the external mycelium of G. intraradices were not affected by the antagonistic fungus T. harzianum; in contrast, T. harzianum was adversely affected by G. intraradices.


* Corresponding author. Mailing address: Plant Pathology Section, Department of Plant Biology, The Royal Veterinary and Agricultural University, Thorvaldsensvej 40, entrance 8, 3rd floor, DK-1871 Frederiksberg C, Copenhagen, Denmark. Phone: 45 35 28 33 06. Fax: 45 35 28 33 10. E-mail: hg{at}kvl.dk.

dagger Present address: Department of Plant Protection, Danish Institute of Agricultural Sciences, Flakkebjerg, DK-4200 Slagelse, Denmark.


Applied and Environmental Microbiology, April 1999, p. 1428-1434, Vol. 65, No. 4
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



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