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转录因子 Liv4 是新型隐球菌生长和发病所必需的。

Transcription factor Liv4 is required for growth and pathogenesis of Cryptococcus neoformans.

机构信息

Department of Dermatology, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai, 200003, China.

Shanghai Key Laboratory of Molecular Medical Mycology, Shanghai Institute of Medical Mycology, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai, 200003, China.

出版信息

FEMS Yeast Res. 2020 May 1;20(3). doi: 10.1093/femsyr/foaa015.

Abstract

Cryptococcus neoformans is an important invasive fungal pathogen that causes life-threatening meningoencephalitis in humans. Its biological and pathogenic regulatory mechanisms remain largely unknown, particularly due to the presence of those core transcription factors (TFs). Here, we conducted a detailed characterization of the TF Liv4 in the biology and virulence of C. neoformans. Deletion of TF Liv4 protein resulted in growth defect under both normal and stress conditions (such as high temperature and cell wall/membrane damaging agents), drastic morphological damage and also attenuated virulence in C. neoformans. These phenotypic changes might be contributed to transcriptional abnormality in the liv4Δ mutant, in which several cryptococcal genes involved in energy metabolism and cell wall integrity were downregulated. Furthermore, ChIP-seq and ChIP-qPCR assays suggested TF Liv4 might exert its regulatory function in transcription by its activation of RBP1 in C. neoformans. Taken together, our work highlights the importance of TF Liv4 in the growth and virulence of C. neoformans, and it facilitates a better understanding of cryptococcal pathogenesis mechanisms.

摘要

新生隐球菌是一种重要的侵袭性真菌病原体,可导致人类致命性脑膜脑炎。其生物学和发病机制的调节机制在很大程度上尚不清楚,特别是由于存在那些核心转录因子(TFs)。在这里,我们对新生隐球菌生物学和毒力中的 TF Liv4 进行了详细的表征。TF Liv4 蛋白缺失导致正常和应激条件(如高温和细胞壁/膜损伤剂)下的生长缺陷、形态严重损伤,并降低了新生隐球菌的毒力。这些表型变化可能归因于 liv4Δ 突变体中的转录异常,其中涉及能量代谢和细胞壁完整性的几个隐球菌基因下调。此外,ChIP-seq 和 ChIP-qPCR 分析表明,TF Liv4 可能通过激活新生隐球菌中的 RBP1 发挥其转录调控功能。总之,我们的工作强调了 TF Liv4 在新生隐球菌生长和毒力中的重要性,并有助于更好地理解隐球菌发病机制。

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