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Microbiology (Reading). 2023 Jan;169(1). doi: 10.1099/mic.0.001286.
5
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9
Highly accurate protein structure prediction with AlphaFold.利用 AlphaFold 进行高精度蛋白质结构预测。
Nature. 2021 Aug;596(7873):583-589. doi: 10.1038/s41586-021-03819-2. Epub 2021 Jul 15.
10
The Brilliance of Mechanisms of Host Immune Evasion by Lyme Disease-Causing Spirochetes.莱姆病螺旋体宿主免疫逃逸机制的卓越之处
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伯氏疏螺旋体哺乳动物感染期间bb0556的表达及其作用分析

Analysis of bb0556 Expression and Its Role During Borrelia burgdorferi Mammalian Infection.

作者信息

George Sierra, Waldron Connor, Thompson Christina, Ouyang Zhiming

机构信息

Department of Molecular Medicine, University of South Florida, Tampa, Florida, USA.

出版信息

Mol Microbiol. 2024 Dec;122(6):831-846. doi: 10.1111/mmi.15319. Epub 2024 Sep 20.

DOI:10.1111/mmi.15319
PMID:39305042
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11659052/
Abstract

In Borrelia burgdorferi, BB0556 was annotated as a conserved hypothetical protein. We herein investigated gene expression and the importance of this protein during infection. Our data support that bb0556 forms an operon with five other genes. A transcriptional start site and the associated σ-type promoter were identified in the sequences upstream of bb0554, and luciferase reporter assays indicated that this promoter is functional in B. burgdorferi. Furthermore, the sequences upstream of bb0556 contain an internal promoter to drive gene expression. bb0556 expression was affected by various environmental factors such as changes in temperature, pH, and cell density when B. burgdorferi was grown in vitro. Surprisingly, significant differences were observed for bb0556 expression between B. burgdorferi strains B31-A3 and CE162, likely due to the different cis- and trans-acting factors in these strains. Moreover, bb0556 was found to be highly expressed by B. burgdorferi in infected mice tissues, suggesting that this gene plays an important role during animal infection. To test this hypothesis, we generated a bb0556 deletion mutant in a virulent bioluminescent B. burgdorferi strain. The mutant grew normally in the medium and displayed no defect in the resistance to environmental stresses such as reactive oxygen species, reactive nitrogen species, and osmotic stress. However, when the infectivity was compared between the mutant and its parental strain using in vivo bioluminescence imaging as well as analyses of spirochete recovery and bacterial burdens in animal tissues, our data showed that, contrary to the parental strain, the mutant was unable to infect mice. Complementation of bb0556 in cis fully restored the infectious phenotype to wild-type levels. Taken together, our study demonstrates that the hypothetical protein BB0556 is a novel virulence factor essential for B. burgdorferi mammalian infection.

摘要

在伯氏疏螺旋体中,BB0556被注释为一个保守的假定蛋白。我们在此研究了该蛋白在感染过程中的基因表达及其重要性。我们的数据支持bb0556与其他五个基因形成一个操纵子。在bb0554上游序列中鉴定出一个转录起始位点及相关的σ型启动子,荧光素酶报告基因检测表明该启动子在伯氏疏螺旋体中具有功能。此外,bb0556上游序列包含一个内部启动子来驱动基因表达。当伯氏疏螺旋体在体外培养时,bb0556的表达受多种环境因素影响,如温度、pH值和细胞密度的变化。令人惊讶的是,在伯氏疏螺旋体菌株B31 - A3和CE162之间观察到bb0556表达存在显著差异,这可能是由于这些菌株中不同的顺式和反式作用因子所致。此外,发现bb0556在感染小鼠组织中的伯氏疏螺旋体中高度表达,表明该基因在动物感染过程中起重要作用。为了验证这一假设,我们在一株具有毒力的生物发光伯氏疏螺旋体菌株中构建了bb0556缺失突变体。该突变体在培养基中生长正常,在对活性氧、活性氮和渗透胁迫等环境应激的抗性方面没有缺陷。然而,当使用体内生物发光成像以及分析动物组织中的螺旋体恢复情况和细菌载量来比较突变体与其亲本菌株的感染性时,我们的数据显示,与亲本菌株相反,突变体无法感染小鼠。顺式互补bb0556可将感染表型完全恢复到野生型水平。综上所述,我们的研究表明,假定蛋白BB0556是伯氏疏螺旋体哺乳动物感染所必需的一种新型毒力因子。