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全基因组搜索铁限制条件下双歧杆菌生长所需基因

Genome-Wide Search for Genes Required for Bifidobacterial Growth under Iron-Limitation.

作者信息

Lanigan Noreen, Bottacini Francesca, Casey Pat G, O'Connell Motherway Mary, van Sinderen Douwe

机构信息

APC Microbiome Institute and School of Microbiology, University College CorkCork, Ireland.

出版信息

Front Microbiol. 2017 May 31;8:964. doi: 10.3389/fmicb.2017.00964. eCollection 2017.

Abstract

Bacteria evolved over millennia in the presence of the vital micronutrient iron. Iron is involved in numerous processes within the cell and is essential for nearly all living organisms. The importance of iron to the survival of bacteria is obvious from the large variety of mechanisms by which iron may be acquired from the environment. Random mutagenesis and global gene expression profiling led to the identification of a number of genes, which are essential for UCC2003 survival under iron-restrictive conditions. These genes encode, among others, Fe-S cluster-associated proteins, a possible ferric iron reductase, a number of cell wall-associated proteins, and various DNA replication and repair proteins. In addition, our study identified several presumed iron uptake systems which were shown to be essential for UCC2003 growth under conditions of either ferric and/or ferrous iron chelation. Of these, two gene clusters encoding putative iron-uptake systems, and , were further characterised, indicating that is involved in ferrous iron transport, while the -encoded transport system imports both ferrous and ferric iron. Transcription studies showed that and constitute two separate transcriptional units that are induced upon dipyridyl-mediated iron limitation. In the anaerobic gastrointestinal environment ferrous iron is presumed to be of most relevance, though a mutation in the cluster does not affect UCC2003's ability to colonise the gut of a murine model.

摘要

细菌在重要的微量营养素铁的存在下历经数千年进化而来。铁参与细胞内的众多过程,对几乎所有生物都至关重要。从可从环境中获取铁的多种机制可以明显看出铁对细菌生存的重要性。随机诱变和全基因组表达谱分析导致鉴定出许多基因,这些基因对于UCC2003在铁限制条件下的生存至关重要。这些基因除其他外还编码铁硫簇相关蛋白、一种可能的三价铁还原酶、一些细胞壁相关蛋白以及各种DNA复制和修复蛋白。此外,我们的研究确定了几种推测的铁摄取系统,这些系统在三价铁和/或二价铁螯合条件下对UCC2003的生长至关重要。其中,对编码假定铁摄取系统的两个基因簇 和 进行了进一步表征,表明 参与二价铁运输,而 编码的运输系统可导入二价铁和三价铁。转录研究表明, 和 构成两个独立的转录单元,在联吡啶介导的铁限制下被诱导。在厌氧的胃肠道环境中,推测二价铁最为相关,尽管 簇中的突变并不影响UCC2003定殖于小鼠模型肠道的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b543/5449479/938965de6781/fmicb-08-00964-g0001.jpg

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