Department of Molecular Medicine, University of South Florida, Tampa, Florida, USA.
Infect Immun. 2023 Mar 15;91(3):e0053922. doi: 10.1128/iai.00539-22. Epub 2023 Feb 6.
The alternative sigma factor RpoS in Borrelia burgdorferi, the etiological agent of Lyme disease, has long been postulated to regulate virulence-associated genes other than and . Here, we demonstrate that , a gene encoding a hypothetical protein, is regulated by RpoS and contributes to the optimal infectivity of B. burgdorferi. When B. burgdorferi was exposed to environmental stimuli, showed similar expression patterns as , , and . Expression of was significantly downregulated when was inactivated and was restored in the complemented strain. By using rapid amplification of cDNA ends (RACE) and luciferase reporter assays, a functional promoter was identified in the regulatory region upstream of . Gene expression from this promoter was drastically decreased in the mutant. We next investigated the role of during animal infection. By using quantitative reverse transcription-PCR (RT-PCR), we found that was highly expressed in mouse tissues during infection. We further created a -deficient mutant in a bioluminescent B. burgdorferi strain and examined infection dynamics using imaging. Relative to the parental and complemented strains, the mutant showed a delayed infection pattern and bacterial load was reduced. Another deletion mutant was also created in the strain 297 background, and quantitative PCR (qPCR) analysis revealed a significantly lower spirochetal burden in tissue samples collected from animals infected with the mutant. In addition, localization studies indicate that BB0563 is not exposed on the cell surface but is associated with outer membrane. Taken together, these results suggest that is required for optimal infectivity of B. burgdorferi during experimental infection.
伯氏疏螺旋体(Borrelia burgdorferi)是莱姆病的病原体,其替代 sigma 因子 RpoS 长期以来被认为可以调节除 和 以外的与毒力相关的基因。在这里,我们证明编码一个假定蛋白的基因 受 RpoS 调控,并有助于伯氏疏螺旋体的最佳感染性。当伯氏疏螺旋体暴露于环境刺激时, 表现出与 、 、相似的表达模式。当 失活时, 的表达显著下调,并在互补菌株中得到恢复。通过使用快速扩增 cDNA 末端 (RACE) 和荧光素酶报告基因分析,在 的调控区上游鉴定出一个功能启动子。该启动子的基因表达在 突变体中明显降低。我们接下来研究了 在动物感染中的作用。通过使用定量逆转录-PCR (RT-PCR),我们发现 在感染过程中在小鼠组织中高度表达。我们进一步在发光伯氏疏螺旋体菌株中创建了一个 -缺陷突变体,并使用 成像检查感染动力学。与亲本和互补菌株相比,突变体显示出延迟的感染模式和细菌负荷降低。还在 297 背景的菌株中创建了另一个 缺失突变体,定量 PCR (qPCR)分析显示感染突变体的动物组织样本中的螺旋体负担明显降低。此外,定位研究表明 BB0563 不暴露在细胞表面,而是与外膜相关。总之,这些结果表明 在实验感染期间伯氏疏螺旋体的最佳感染性是必需的。