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WS-5995 B,an antifungal agent inducing differential gene expression in the conifer pathogen <Emphasis Type="Italic">Heterobasidion annosum</Emphasis> but not in <Emphasis Type="Italic">Heterobasidion abietinum</Emphasis>
Authors:Nina A Lehr  Aleksandra Adomas  Frederick O Asiegbu  Rüdiger Hampp  Mika T Tarkka
Institution:1.Faculty of Biology, Institute of Microbiology,University of Tübingen,Tübingen,Germany;2.Department of Forest Mycology and Pathology,Swedish University of Agricultural Sciences,Uppsala,Sweden;3.Department of Forest Ecology, Faculty of Agriculture and Forestry,University of Helsinki,Helsinki,Finland;4.Department of Soil Ecology,UFZ, Helmholtz-Centre for Environmental Research,Halle,Germany;5.School of Biosciences,University of Exeter,Exeter,UK
Abstract:The mycorrhization helper bacterium Streptomyces sp. AcH 505 inhibits Norway spruce root infection and colonisation by the root and butt rot fungus Heterobasidion annosum 005 but not by the congeneric strain Heterobasidion abietinum 331 because of higher sensitivity of H. annosum 005 towards the AcH 505-derived naphthoquinone antibiotic WS-5995 B. Differences in antibiotic sensitivity between two isolates belonging to two species, H. annosum 005 and H. abietinum 331, were investigated by comparative gene expression analysis using macroarrays and quantitative RT-PCR after WS-5995 B, structurally related mollisin and unrelated cycloheximide application. Treatment with 25 μM WS-5995 B for 2 h resulted in a significant up-regulation of expression of inosine-5′-monophosphate dehydrogenase, phosphoglucomutase and GTPase genes, while the expression of genes encoding for thioredoxin and glutathione dependent formaldehyde dehydrogenase was down-regulated in the sensitive fungal strain. No differential expression in the tolerant strain was detected. Application of WS-5995 B at higher concentrations over a time course experiment revealed that H. annosum 005 and H. abietinum 331 responded differently to WS-5995 B. The fungal gene expression levels depended on both the concentration of WS-5995 B and the duration of its application. The WS-5995 B-unrelated cycloheximide caused highly specific changes in patterns of gene expression. Our findings indicate considerable variations in response to bacterial metabolites by the isolates of the conifer pathogen.
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