Leibniz Institute for Natural Product Research and Infection Biology - Hans Knoell Institute, Junior Research Group Fundamental Molecular Biology of Pathogenic Fungi, Beutenbergstr. 11a, D-07745 Jena, Germany.
Department of Dermatology, Centre Hospitalier Universitaire Vaudois, Av. de Beaumont 29, 1011 Lausanne, Switzerland.
Microbiology (Reading). 2010 Mar;156(Pt 3):884-895. doi: 10.1099/mic.0.033464-0. Epub 2009 Nov 26.
Although dermatophytes are the most common agents of superficial mycoses in humans and animals, the molecular basis of the pathogenicity of these fungi is largely unknown. In vitro digestion of keratin by dermatophytes is associated with the secretion of multiple proteases, which are assumed to be responsible for their particular specialization to colonize and degrade keratinized host structures during infection. To investigate the role of individual secreted proteases in dermatophytosis, a guinea pig infection model was established for the zoophilic dermatophyte Arthroderma benhamiae, which causes highly inflammatory cutaneous infections in humans and rodents. By use of a cDNA microarray covering approximately 20-25 % of the A. benhamiae genome and containing sequences of at least 23 protease genes, we revealed a distinct in vivo protease gene expression profile in the fungal cells, which was surprisingly different from the pattern elicited during in vitro growth on keratin. Instead of the major in vitro -expressed proteases, others were activated specifically during infection. These enzymes are therefore suggested to fulfil important functions that are not exclusively associated with the degradation of keratin. Most notably, the gene encoding the serine protease subtilisin 6, which is a known major allergen in the related dermatophyte Trichophyton rubrum and putatively linked to host inflammation, was found to be the most strongly upregulated gene during infection. In addition, our approach identified other candidate pathogenicity-related factors in A. benhamiae, such as genes encoding key enzymes of the glyoxylate cycle and an opsin-related protein. Our work provides what we believe to be the first broad-scale gene expression profile in human pathogenic dermatophytes during infection, and points to putative virulence-associated mechanisms that make these micro-organisms the most successful aetiological agents of superficial mycoses.
虽然皮肤真菌是人类和动物中最常见的浅部真菌病病原体,但这些真菌的致病性的分子基础在很大程度上仍是未知的。皮肤真菌对角蛋白的体外消化与多种蛋白酶的分泌有关,这些蛋白酶被认为是它们在感染过程中特异地定殖和降解角蛋白宿主结构的原因。为了研究单个分泌蛋白酶在皮肤真菌病中的作用,我们建立了一种豚鼠感染模型,用于研究亲动物性的皮肤真菌须毛癣菌,该真菌可引起人类和啮齿动物的高度炎症性皮肤感染。通过使用包含大约 20-25%的须毛癣菌基因组序列和至少 23 个蛋白酶基因序列的 cDNA 微阵列,我们揭示了真菌细胞中一种独特的体内蛋白酶基因表达谱,这与在角蛋白上体外生长时所诱导的模式惊人地不同。在感染过程中,替代主要的体外表达蛋白酶,其他蛋白酶被特异性激活。因此,这些酶被认为具有重要的功能,而不仅仅与角蛋白的降解有关。值得注意的是,编码丝氨酸蛋白酶枯草杆菌蛋白酶 6 的基因,它是相关真菌须癣毛癣菌中的一种主要过敏原,并且推测与宿主炎症有关,在感染过程中被发现是上调最明显的基因。此外,我们的方法还鉴定了须毛癣菌中的其他候选致病性相关因素,如编码乙醛酸循环关键酶和视蛋白相关蛋白的基因。我们的工作提供了我们认为是感染过程中人类致病性皮肤真菌的第一个广泛的基因表达谱,并指出了潜在的与毒力相关的机制,这些机制使这些微生物成为最成功的浅部真菌病的病因。