Faculty of Biology, Institute of Microbiology, University of Tübingen, Tübingen, Germany.
Appl Microbiol Biotechnol. 2009 Nov;85(2):347-58. doi: 10.1007/s00253-009-2254-7. Epub 2009 Oct 2.
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 microM 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.
共生菌 Helper bacterium Streptomyces sp. AcH 505 抑制挪威云杉根感染和腐烂菌 Heterobasidion annosum 005 的定殖,但不能抑制同属菌株 Heterobasidion abietinum 331,因为 H. annosum 005 对 AcH 505 衍生的萘醌抗生素 WS-5995 B 更敏感。通过比较基因表达分析,使用 macroarrays 和定量 RT-PCR 研究了属于两个物种的两个分离物(H. annosum 005 和 H. abietinum 331)之间的抗生素敏感性差异,在 WS-5995 B、结构相关的 mollisin 和不相关的环己酰亚胺应用后进行。用 25 μM WS-5995 B 处理 2 小时导致肌苷-5'-单磷酸脱氢酶、磷酸葡萄糖变位酶和 GTPase 基因的表达显著上调,而编码硫氧还蛋白和谷胱甘肽依赖的甲醛脱氢酶的基因表达下调在敏感真菌菌株中。在耐受菌株中未检测到差异表达。在时间过程实验中用较高浓度的 WS-5995 B 进行应用表明,H. annosum 005 和 H. abietinum 331 对 WS-5995 B 的反应不同。真菌基因表达水平取决于 WS-5995 B 的浓度和应用时间。WS-5995 B 不相关的环己酰亚胺引起基因表达模式的高度特异性变化。我们的研究结果表明,对细菌代谢物的反应在针叶树病原体的分离物中有很大的变化。