Sierra George, Connor Waldron, Christina Thompson, Zhiming Ouyang
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Surprisingly, significant differences were observed for <i>bb0556</i> expression between <i>B. burgdorferi</i> strains B31-A3 and CE162, likely due to the different <i>cis-</i> and <i>trans</i>-acting factors in these strains. Moreover, <i>bb0556</i> was found to be highly expressed by <i>B. burgdorferi</i> in infected mice tissues, suggesting that this gene plays an important role during animal infection. To test this hypothesis, we generated a <i>bb0556</i> deletion mutant in a virulent bioluminescent <i>B. burgdorferi</i> 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 <i>bb0556</i> in <i>cis</i> 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 <i>B. burgdorferi</i> mammalian infection.","PeriodicalId":19006,"journal":{"name":"Molecular Microbiology","volume":"11 1","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2024-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Analysis of bb0556 Expression and Its Role During Borrelia burgdorferi Mammalian Infection\",\"authors\":\"Sierra George, Connor Waldron, Christina Thompson, Zhiming Ouyang\",\"doi\":\"10.1111/mmi.15319\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In <i>Borrelia burgdorferi</i>, 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 <i>bb0556</i> forms an operon with five other genes. A transcriptional start site and the associated σ<sup>70</sup>-type promoter were identified in the sequences upstream of <i>bb0554</i>, and luciferase reporter assays indicated that this promoter is functional in <i>B. burgdorferi</i>. Furthermore, the sequences upstream of <i>bb0556</i> contain an internal promoter to drive gene expression. <i>bb0556</i> expression was affected by various environmental factors such as changes in temperature, pH, and cell density when <i>B. burgdorferi</i> was grown in vitro. Surprisingly, significant differences were observed for <i>bb0556</i> expression between <i>B. burgdorferi</i> strains B31-A3 and CE162, likely due to the different <i>cis-</i> and <i>trans</i>-acting factors in these strains. Moreover, <i>bb0556</i> was found to be highly expressed by <i>B. burgdorferi</i> in infected mice tissues, suggesting that this gene plays an important role during animal infection. 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引用次数: 0
摘要
在鲍曼不动杆菌中,BB0556 被注释为一种保守的假定性蛋白。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作子。在 bb0554 的上游序列中发现了一个转录起始位点和相关的 σ70 型启动子,荧光素酶报告实验表明该启动子在 B. burgdorferi 中具有功能。此外,bb0556 的上游序列包含一个内部启动子,可驱动基因表达。在 B. burgdorferi 体外生长时,bb0556 的表达受各种环境因素的影响,如温度、pH 值和细胞密度的变化。令人惊讶的是,在 B. burgdorferi 菌株 B31-A3 和 CE162 之间观察到了 bb0556 表达的显著差异,这可能是由于这些菌株中的顺式和反式作用因子不同所致。此外,我们还发现 bb0556 在受感染的小鼠组织中高度表达,这表明该基因在动物感染过程中发挥着重要作用。为了验证这一假设,我们在一株毒性生物发光杆菌中产生了一个 bb0556 缺失突变体。该突变体在培养基中生长正常,对活性氧、活性氮和渗透压等环境胁迫的抵抗力也没有缺陷。然而,当我们使用体内生物发光成像以及螺旋体恢复和动物组织中细菌负荷分析来比较突变体及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。bb0556 的顺式互补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,假说蛋白 BB0556 是一种新型毒力因子,对 B. burgdorferi 感染哺乳动物至关重要。
Analysis of bb0556 Expression and Its Role During Borrelia burgdorferi Mammalian Infection
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 σ70-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.
期刊介绍:
Molecular Microbiology, the leading primary journal in the microbial sciences, publishes molecular studies of Bacteria, Archaea, eukaryotic microorganisms, and their viruses.
Research papers should lead to a deeper understanding of the molecular principles underlying basic physiological processes or mechanisms. Appropriate topics include gene expression and regulation, pathogenicity and virulence, physiology and metabolism, synthesis of macromolecules (proteins, nucleic acids, lipids, polysaccharides, etc), cell biology and subcellular organization, membrane biogenesis and function, traffic and transport, cell-cell communication and signalling pathways, evolution and gene transfer. Articles focused on host responses (cellular or immunological) to pathogens or on microbial ecology should be directed to our sister journals Cellular Microbiology and Environmental Microbiology, respectively.