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Applied and Environmental Microbiology, February 2008, p. 931-941, Vol. 74, No. 4
0099-2240/08/$08.00+0     doi:10.1128/AEM.01158-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Detection and Identification of Fungi Intimately Associated with the Brown Seaweed Fucus serratus{triangledown} ,{dagger}

Alga Zuccaro,1* Conrad L. Schoch,2 Joseph W. Spatafora,2 Jan Kohlmeyer,3 Siegfried Draeger,1 and Julian I. Mitchell4

Institute of Phytopathology and Applied Zoology, University of Giessen, D-35392 Giessen, Germany,1 Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon 97331,2 Institute of Marine Sciences, University of North Carolina, Morehead City, North Carolina 28557,3 School of Biological Sciences, University of Portsmouth, Portsmouth PO1 2DY, United Kingdom4

Received 23 May 2007/ Accepted 1 December 2007

The filamentous fungi associated with healthy and decaying Fucus serratus thalli were studied over a 1-year period using isolation methods and molecular techniques such as 28S rRNA gene PCR-denaturing gradient gel electrophoresis (DGGE) and phylogenetic and real-time PCR analyses. The predominant DGGE bands obtained from healthy algal thalli belonged to the Lindra, Lulworthia, Engyodontium, Sigmoidea/Corollospora complex, and Emericellopsis/Acremonium-like ribotypes. In the culture-based analysis the incidence of recovery was highest for Sigmoidea marina isolates. In general, the environmental sequences retrieved could be matched unambiguously to isolates recovered from the seaweed except for the Emericellopsis/Acremonium-like ribotype, which showed 99% homology with the sequences of four different isolates, including that of Acremonium fuci. To estimate the extent of colonization of A. fuci, we used a TaqMan real-time quantitative PCR assay for intron 3 of the beta-tubulin gene, the probe for which proved to be species specific even when it was used in amplifications with high background concentrations of other eukaryotic DNAs. The A. fuci sequence was detected with both healthy and decaying thalli, but the signal was stronger for the latter. Additional sequence types, representing members from the Dothideomycetes, were recovered from the decaying thallus DNA, which suggested that a change in fungal community structure had occurred. Phylogenetic analysis of these environmental sequences and the sequences of isolates and type species indicated that the environmental sequences were novel in the Dothideomycetes.


* Corresponding author. Mailing address: Justus-Liebig Universität Giessen, Institute of Phytopathology and Applied Zoology, Heinrich-Buff-Ring 26-32, D-35392 Giessen, Germany. Phone: 49 641 99-37497. Fax: 49 641 99-37499. E-mail: Alga.Zuccaro{at}agrar.uni-giessen.de

{triangledown} Published ahead of print on 14 December 2007.

{dagger} Supplemental material for this article may be found at http://aem.asm.org/.


Applied and Environmental Microbiology, February 2008, p. 931-941, Vol. 74, No. 4
0099-2240/08/$08.00+0     doi:10.1128/AEM.01158-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







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