Ramsey Kathryn M, Dove Simon L
Division of Infectious Diseases, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Mol Microbiol. 2016 Aug;101(4):688-700. doi: 10.1111/mmi.13418. Epub 2016 Jun 10.
The orphan response regulator PmrA is essential for the intramacrophage growth and survival of Francisella tularensis. PmrA was thought to promote intramacrophage growth by binding directly to promoters on the Francisella Pathogenicity Island (FPI) and positively regulating the expression of FPI genes, which encode a Type VI secretion system required for intramacrophage growth. Using both ChIP-Seq and RNA-Seq we identify those regions of the F. tularensis chromosome occupied by PmrA and those genes that are regulated by PmrA. We find that PmrA associates with 252 distinct regions of the F. tularensis chromosome, but exerts regulatory effects at only a few of these locations. Rather than by functioning directly as an activator of FPI gene expression we present evidence that PmrA promotes intramacrophage growth by repressing the expression of a single target gene we refer to as priM (PmrA-repressed inhibitor of intramacrophage growth). Our findings thus indicate that the role of PmrA in facilitating intracellular growth is to repress a previously unknown anti-virulence factor. PriM is the first bacterially encoded factor to be described that can interfere with the intramacrophage growth and survival of F. tularensis.
孤儿应答调节因子PmrA对于土拉弗朗西斯菌在巨噬细胞内的生长和存活至关重要。PmrA被认为通过直接结合土拉弗朗西斯菌致病岛(FPI)上的启动子并正向调节FPI基因的表达来促进巨噬细胞内生长,这些基因编码巨噬细胞内生长所需的VI型分泌系统。我们使用染色质免疫沉淀测序(ChIP-Seq)和RNA测序(RNA-Seq)技术来确定被PmrA占据的土拉弗朗西斯菌染色体区域以及受PmrA调控的基因。我们发现PmrA与土拉弗朗西斯菌染色体的252个不同区域相关联,但仅在其中少数位置发挥调控作用。我们提供的证据表明,PmrA并非直接作为FPI基因表达的激活因子发挥作用,而是通过抑制一个我们称为priM(PmrA抑制的巨噬细胞内生长抑制剂)的单一靶基因的表达来促进巨噬细胞内生长。因此,我们的研究结果表明,PmrA在促进细胞内生长中的作用是抑制一种先前未知的抗毒力因子。PriM是首个被描述的可干扰土拉弗朗西斯菌在巨噬细胞内生长和存活的细菌编码因子。