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An Ssd1 Homolog Impacts Trehalose and Chitin Biosynthesis and Contributes to Virulence in Aspergillus fumigatus

机译:Ssd1同源物影响海藻糖和几丁质的生物合成,并有助于烟曲霉的毒力。

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Regulation of fungal cell wall biosynthesis is critical to maintain cell wall integrity in dynamic fungal infection microenvironments. Genes involved in this response that impact fungal fitness and host immune responses remain to be fully defined. In this study, we observed that a yeast ssd1 homolog, ssdA , in the filamentous fungus Aspergillus fumigatus is involved in trehalose and cell wall homeostasis. An ssdA null mutant strain exhibited an increase in trehalose levels and a reduction in fungal colony growth rate. In contrast, overexpression of ssdA perturbed trehalose biosynthesis and reduced germination of conidia. The ssdA null mutant strain was more resistant to cell wall-perturbing agents, while overexpression of ssdA increased sensitivity. Overexpression of ssdA significantly increased chitin levels, and both loss and overexpression of ssdA altered subcellular localization of the class V chitin synthase CsmA. Strikingly, overexpression of ssdA abolished adherence to abiotic surfaces and severely attenuated the virulence of A. fumigatus in a murine model of invasive pulmonary aspergillosis. Despite the severe in vitro fitness defects observed upon loss of ssdA , neither surface adherence nor murine survival was impacted. In conclusion, A. fumigatus SsdA plays a critical role in cell wall homeostasis impacting A. fumigatus -host interactions. IMPORTANCE The incidence of life-threatening infections caused by the filamentous fungus Aspergillus fumigatus is increasing along with an increase in the number of fungal strains resistant to contemporary antifungal therapies. The fungal cell wall and the associated carbohydrates required for its synthesis and maintenance are attractive drug targets given that many genes encoding proteins involved in cell wall biosynthesis and integrity are absent in humans. Importantly, genes and associated cell wall biosynthesis and homeostasis regulatory pathways remain to be fully defined in A. fumigatus . In this report, we identify SsdA as an important component of trehalose and fungal cell wall biosynthesis in A. fumigatus that consequently impacts the host immune response and fungal virulence in animal models of infection.
机译:真菌细胞壁生物合成的调控对于在动态真菌感染微环境中维持细胞壁完整性至关重要。影响真菌适应性和宿主免疫反应的基因尚待充分定义。在这项研究中,我们观察到丝状真菌烟曲霉中的酵母ssd1同源物ssdA与海藻糖和细胞壁稳态有关。 ssdA null突变菌株显示出海藻糖水平升高和真菌菌落生长速率降低。相反,ssdA的过表达干扰了海藻糖的生物合成,降低了分生孢子的萌发。 ssdA无效突变株对细胞壁扰动剂更具抗性,而ssdA的过表达则增加了敏感性。 ssdA的过表达显着增加了几丁质水平,并且ssdA的丢失和过表达都改变了V类几丁质合酶CsmA的亚细胞定位。令人惊讶的是,在侵袭性肺曲霉病的小鼠模型中,ssdA的过表达消除了对非生物表面的粘附并严重减弱了烟曲霉的毒力。尽管丢失ssdA时观察到严重的体外适应性缺陷,但表面附着力和鼠的存活率均未受影响。总之,烟曲霉SsdA在影响烟曲霉-宿主相互作用的细胞壁稳态中起关键作用。重要性由丝状真菌烟曲霉(Aspergillus fumigatus)引起的威胁生命的感染的发生率随着对现代抗真菌疗法产生耐药性的真菌菌株数量的增加而增加。鉴于人类中缺少许多编码涉及细胞壁生物合成和完整性的蛋白质的基因,真菌细胞壁及其合成和维持所需的相关碳水化合物是有吸引力的药物靶标。重要的是,在烟曲霉中,基因和相关的细胞壁生物合成及稳态调节途径仍有待完全定义。在此报告中,我们确定SsdA是烟曲霉中海藻糖和真菌细胞壁生物合成的重要组成部分,从而影响感染动物模型中的宿主免疫反应和真菌毒力。

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