4.6 Article

The two Pseudomonas aeruginosa DksA stringent response proteins are largely interchangeable at the whole transcriptome level and in the control of virulence-related traits

期刊

ENVIRONMENTAL MICROBIOLOGY
卷 23, 期 9, 页码 5487-5504

出版社

WILEY
DOI: 10.1111/1462-2920.15693

关键词

-

资金

  1. Italian Ministry for Education, University and Research [RBFR10LHD1_002, 20177J5Y3P]
  2. Italian Cystic FibrosisResearch Foundation [FFC 17/2018]
  3. Grant of Excellence Departments, MIUR-Italy [COMMI 314 -337 LEGGE 232/2016]

向作者/读者索取更多资源

DksA1 and DksA2 play critical roles in P. aeruginosa environmental adaptation, largely interchangeable with each other. While most genes' expression levels are restored by either dksA1 or dksA2, a small subset of genes seems to be preferentially complemented by one of them.
The stringent response regulator DksA plays a key role in Gram negative bacteria adaptation to challenging environments. Intriguingly, the plant and human pathogen Pseudomonas aeruginosa is unique as it expresses two functional DksA paralogs: DksA1 and DksA2. However, the role of DksA2 in P. aeruginosa adaptive strategies has been poorly investigated so far. Here, RNA-Seq analysis and phenotypic assays showed that P. aeruginosa DksA1 and DksA2 proteins are largely interchangeable. Relative to wild type P. aeruginosa, transcription of 1779 genes was altered in a dksA1 dksA2 double mutant, and the wild type expression level of >= 90% of these genes was restored by in trans complementation with either dksA1 or dksA2. Interestingly, the expression of a small sub-set of genes seems to be preferentially or exclusively complemented by either dksA1 or dksA2. In addition, evidence has been provided that the DksA-dependent regulation of virulence genes expression is independent and hierarchically dominant over two major P. aeruginosa regulatory circuits, i.e., quorum sensing and cyclic-di-GMP signalling systems. Our findings support the prominent role of both DksA paralogs in P. aeruginosa environmental adaptation.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据