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首页> 外文期刊>Medical mycology: official publication of the International Society for Human and Animal Mycology >Afyap1, encoding a bZip transcriptional factor of Aspergillus fumigatus, contributes to oxidative stress response but is not essential to the virulence of this pathogen in mice immunosuppressed by cyclophosphamide and triamcinolone.
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Afyap1, encoding a bZip transcriptional factor of Aspergillus fumigatus, contributes to oxidative stress response but is not essential to the virulence of this pathogen in mice immunosuppressed by cyclophosphamide and triamcinolone.

机译:编码烟曲霉的bZip转录因子的Afyap1有助于氧化应激反应,但对于被环磷酰胺和曲安西龙免疫抑制的小鼠中这种病原体的毒力并不是必需的。

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摘要

Aspergillus fumigatus, an important human fungal pathogen, encounters high levels of reactive oxygen species following its ingestion by phagocytes. Reactive oxygen species are important mediators of the fungicidal activities of phagocytes. In yeasts, YAP1 encodes for transcriptional factors that contribute to their oxidative stress response and given the importance of the stress response, we hypothesized that the YAP1 homologue in A. fumigatus plays a similar role in this fungus. In this study, we found that Afyap1, the Yap1 homologue of A. fumigatus, confers protection against oxidative stress. Replacement of Afyap1 with the marker gene pyrG (DeltaAfyap1) resulted in hypersensitivity of A. fumigatus to oxidants such as H(2)O(2) and menadione. In contrast, an A. fumigatus strain harboring multiple-copy Afyap1 was resistant to these two oxidants as well as the oxidant diamide. However, DeltaAfyap1 and strain harboring multiple-copy Afyap1 were comparable in their virulence to a wild-type A. fumigatus strain in a murine model of invasive pulmonary aspergillosis. Taken together, these results demonstrate that Afyap1 is involved in oxidative stress response but is not an essential virulence factor for A. fumigatus.
机译:烟曲霉是一种重要的人类真菌病原体,在被吞噬细胞摄入后会遇到高水平的活性氧。活性氧是吞噬细胞杀真菌活性的重要介质。在酵母中,YAP1编码有助于其氧化应激反应的转录因子,并且鉴于应激反应的重要性,我们假设烟曲霉中的YAP1同源物在这种真菌中起着相似的作用。在这项研究中,我们发现烟曲霉的Yap1同源物Afyap1赋予了抵抗氧化应激的保护作用。用标记基因pyrG(DeltaAfyap1)替换Afyap1导致了烟曲霉对H(2)O(2)和甲萘醌等氧化剂的超敏性。相反,具有多拷贝Afyap1的烟曲霉菌株对这两种氧化剂以及二酰胺氧化剂均具有抗性。但是,在侵袭性肺曲霉病的小鼠模型中,DeltaAfyap1和带有多拷贝Afyap1的菌株在毒力方面与野生型烟曲霉菌株相当。综上所述,这些结果表明Afyap1参与了氧化应激反应,但不是烟曲霉的必需毒力因子。

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