Host-Parasite Interactions Section, Laboratory of Bacteriology, Rocky Mountain Laboratories, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, USA.
J Bacteriol. 2024 Oct 24;206(10):e0036724. doi: 10.1128/jb.00367-24. Epub 2024 Sep 30.
is an obligate intracellular, tick-borne bacterium that causes Rocky Mountain spotted fever. The demanding nature of cultivating these bacteria within host cells and the labor involved in obtaining clonal isolates have severely limited progress regarding the development of compatible genetic tools to study this pathogen. Conditional expression of genes that might be toxic or have an otherwise undesirable effect is the next logical goal to expand upon the constitutive expression plasmids generated thus far. We describe the construction of an inducible promoter system based on the tet-On system, leveraging design elements from the anhydrotetracycline-inducible promoter system used for and one of the few characterized rickettsial promoters for the outer membrane gene, (). The functionality of this promoter is demonstrated via fluorescence of induced mScarlet production and was then used to construct a generalized inducible expression vector for . The development of a functional inducible promoter was then applied to the construction of a CRISPR interference plasmid as a means to reduce or essentially silence the transcription of targeted genes. We demonstrate the viability of a simplified, single vector CRISPRi system to disrupt gene expression in targeting the type IV secreted effector and autotransporter peptidase as examples.
This work expands upon the genetic toolbox available for . We describe both an inducible promoter and CRISPRi system compatible with , which may provide key instruments for the development of further tools. The development of an inducible promoter system allows for the overexpression of genes, which might be toxic when expressed constitutively. The CRISPRi system enables the ability to knock down genes with specificity, and critically, genes that may be essential and could not otherwise be knocked out. These developments may provide the foundation for unlocking genetic tools for other pathogens of the order Rickettsiales, such as the , , and for which there are currently no inducible promoters or CRISPRi platforms.
是一种专性细胞内、蜱传的细菌,可引起落矶山斑点热。由于在宿主细胞内培养这些细菌的苛刻性质以及获得克隆分离株所涉及的劳动,严重限制了开发用于研究这种病原体的相容遗传工具的进展。条件表达可能有毒或具有其他不良影响的基因是扩展迄今为止生成的组成型表达质粒的下一个合乎逻辑的目标。我们描述了基于 tet-On 系统的诱导型启动子系统的构建,该系统利用了用于 和少数几种已鉴定的立克次体外膜基因 ()的anhydrotetracycline 诱导型启动子系统的设计元素。通过诱导 mScarlet 产生的荧光证明了该启动子的功能,然后将其用于构建用于 的通用诱导表达载体。诱导型启动子的开发随后应用于构建 CRISPR 干扰质粒,作为减少或基本上沉默靶向基因转录的一种手段。我们证明了简化的单载体 CRISPRi 系统在破坏靶向 IV 型分泌效应物 和自转运蛋白酶 等基因表达方面的可行性。
这项工作扩展了可用于 的遗传工具包。我们描述了与 兼容的诱导型启动子和 CRISPRi 系统,这可能为进一步工具的开发提供关键工具。诱导型启动子系统的开发允许过表达基因,当组成型表达时,这些基因可能有毒。CRISPRi 系统使具有特异性敲低基因的能力成为可能,并且至关重要的是,敲低那些可能是必需的并且不能被敲除的基因。这些发展可能为开发其他立克次体目病原体的遗传工具奠定基础,例如 、 和 ,目前它们没有诱导型启动子或 CRISPRi 平台。