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新型隐球菌中的缺氧感知:类似生物膜的休眠适应机制?

Hypoxia sensing in cryptococcus neoformans: biofilm-like adaptation for dormancy?

作者信息

Moranova Zuzana, Kawamoto Susumu, Raclavsky Vladislav

机构信息

Department of Microbiology, Palacky University, Olomouc, Czech Republic.

出版信息

Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2009 Sep;153(3):189-93. doi: 10.5507/bp.2009.031.

Abstract

BACKGROUND

Cryptococcus neoformans is an obligate aerobic pathogenic yeast causing lung infection typically followed by spread to the central nervous system. During pathogenesis, it relies on well-established virulence factors. This review focuses on the emerging role of cryptococcal adaptation to hypoxia in pathogenesis.

METHODS AND RESULTS

We examined the MedLine database for information on the cryptococcal hypoxia response. While several recent papers describe components of two presumable hypoxia-sensing pathways including description of their target genes, a link of this system to the hypoxic tuning of proliferation is still missing. In addition, an interpretation of this knowledge in respect to the general picture of microbial pathogenesis is lacking.

CONCLUSIONS

There seems to be a striking parallel between biofilm formation in bacteria, which results in chronic dormant infection with the potential for acute outbreaks, and the dormant state of primary infection followed by secondary outbreaks in C. neoformans. We propose a hypothesis that cryptococcal response to hypoxia might be the driving force for developing a state of dormant infection which is characterized by slowed proliferation and extensive changes in transcriptome and phenotype. This state enables C. neoformans to survive in host and possibly develop life-threatening acute outbreaks later. Hence, conventional well-aerated planktonic culture is not a good in vitro model for studying the pathogenesis of infection and we advocate the development of a more adequate model. Our further conclusion is that the ability of the immune system and antifungal agents to cope with hypoxia-adapted cells is crucial for the successful eradication of cryptococcal infection.

摘要

背景

新型隐球菌是一种专性需氧致病酵母,可引起肺部感染,通常随后扩散至中枢神经系统。在发病过程中,它依赖于已确立的毒力因子。本综述聚焦于新型隐球菌在发病过程中对缺氧适应的新作用。

方法与结果

我们在MedLine数据库中检索了有关新型隐球菌缺氧反应的信息。虽然最近有几篇论文描述了两条可能的缺氧感应途径的组成部分,包括对其靶基因的描述,但该系统与增殖的缺氧调节之间的联系仍然缺失。此外,缺乏关于这一知识在微生物发病机制总体情况方面的解读。

结论

细菌中的生物膜形成导致慢性潜伏感染并有可能引发急性暴发,这与新型隐球菌原发性感染的潜伏状态随后继发暴发之间似乎存在显著的相似之处。我们提出一个假说,即新型隐球菌对缺氧的反应可能是形成潜伏感染状态的驱动力,这种状态的特征是增殖减缓以及转录组和表型发生广泛变化。这种状态使新型隐球菌能够在宿主体内存活,并可能在以后引发危及生命的急性暴发。因此,传统的充分通气的浮游培养不是研究感染发病机制的良好体外模型,我们主张开发更合适的模型。我们的进一步结论是,免疫系统和抗真菌药物应对缺氧适应细胞的能力对于成功根除新型隐球菌感染至关重要。

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