• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Role of the Hypothetical Protein BB0563 during Borrelia burgdorferi Infection in Animals. hypothetical protein BB0563 在动物感染伯氏疏螺旋体中的作用。
Infect Immun. 2023 Mar 15;91(3):e0053922. doi: 10.1128/iai.00539-22. Epub 2023 Feb 6.
2
Assessment of the hypothetical protein BB0616 in the murine infection of .评估 hypothetical protein BB0616 在. 感染小鼠中的作用。
Infect Immun. 2024 Jun 11;92(6):e0009024. doi: 10.1128/iai.00090-24. Epub 2024 May 3.
3
Artificial regulation of ospC expression in Borrelia burgdorferi.伯氏疏螺旋体中ospC表达的人工调控。
Mol Microbiol. 2007 Feb;63(4):1259-73. doi: 10.1111/j.1365-2958.2007.05593.x.
4
DksA plays an essential role in regulating the virulence of Borrelia burgdorferi.DksA在调节伯氏疏螺旋体的毒力方面发挥着重要作用。
Mol Microbiol. 2020 Jul;114(1):172-183. doi: 10.1111/mmi.14504. Epub 2020 Apr 14.
5
Inactivation of bb0184, which encodes carbon storage regulator A, represses the infectivity of Borrelia burgdorferi.编码碳储存调节剂 A 的 bb0184 的失活抑制了伯氏疏螺旋体的感染力。
Infect Immun. 2011 Mar;79(3):1270-9. doi: 10.1128/IAI.00871-10. Epub 2010 Dec 20.
6
Analysis of the ospC regulatory element controlled by the RpoN-RpoS regulatory pathway in Borrelia burgdorferi.伯氏疏螺旋体中由RpoN-RpoS调控途径控制的ospC调控元件分析
J Bacteriol. 2005 Jul;187(14):4822-9. doi: 10.1128/JB.187.14.4822-4829.2005.
7
Analysis of promoter elements involved in the transcriptional initiation of RpoS-dependent Borrelia burgdorferi genes.参与RpoS依赖性伯氏疏螺旋体基因转录起始的启动子元件分析。
J Bacteriol. 2004 Nov;186(21):7390-402. doi: 10.1128/JB.186.21.7390-7402.2004.
8
Activation of the RpoN-RpoS regulatory pathway during the enzootic life cycle of Borrelia burgdorferi.在伯氏疏螺旋体的动物源生活周期中,RpoN-RpoS 调节途径的激活。
BMC Microbiol. 2012 Mar 23;12:44. doi: 10.1186/1471-2180-12-44.
9
Two Distinct Mechanisms Govern RpoS-Mediated Repression of Tick-Phase Genes during Mammalian Host Adaptation by , the Lyme Disease Spirochete.两种不同的机制控制着伯氏疏螺旋体在适应哺乳动物宿主过程中通过 RpoS 介导的蜱期基因的抑制。
mBio. 2017 Aug 22;8(4):e01204-17. doi: 10.1128/mBio.01204-17.
10
RpoS is not central to the general stress response in Borrelia burgdorferi but does control expression of one or more essential virulence determinants.RpoS对伯氏疏螺旋体的一般应激反应并非至关重要,但它确实控制着一种或多种关键毒力决定因素的表达。
Infect Immun. 2004 Nov;72(11):6433-45. doi: 10.1128/IAI.72.11.6433-6445.2004.

引用本文的文献

1
Analysis of the BadR regulon in Borrelia burgdorferi.伯氏疏螺旋体中BadR调控子的分析。
BMC Microbiol. 2025 Feb 26;25(1):94. doi: 10.1186/s12866-025-03797-9.
2
contributes to the virulence of in a murine model of Lyme disease.在莱姆病的小鼠模型中,对 的毒力有贡献。
Infect Immun. 2025 Jan 31;93(1):e0045924. doi: 10.1128/iai.00459-24. Epub 2024 Dec 16.
3
Analysis of bb0556 Expression and Its Role During Borrelia burgdorferi Mammalian Infection.伯氏疏螺旋体哺乳动物感染期间bb0556的表达及其作用分析
Mol Microbiol. 2024 Dec;122(6):831-846. doi: 10.1111/mmi.15319. Epub 2024 Sep 20.
4
Assessment of the hypothetical protein BB0616 in the murine infection of .评估 hypothetical protein BB0616 在. 感染小鼠中的作用。
Infect Immun. 2024 Jun 11;92(6):e0009024. doi: 10.1128/iai.00090-24. Epub 2024 May 3.

本文引用的文献

1
BB0761, a MepM homolog, contributes to Borrelia burgdorferi cell division and mammalian infectivity.BB0761,一种 MepM 同源物,有助于伯氏疏螺旋体的细胞分裂和哺乳动物的感染性。
Mol Microbiol. 2022 Jun;117(6):1405-1418. doi: 10.1111/mmi.14916. Epub 2022 May 16.
2
AlphaFold Protein Structure Database: massively expanding the structural coverage of protein-sequence space with high-accuracy models.AlphaFold 蛋白质结构数据库:用高精度模型极大地扩展蛋白质序列空间的结构覆盖范围。
Nucleic Acids Res. 2022 Jan 7;50(D1):D439-D444. doi: 10.1093/nar/gkab1061.
3
BB0562 is a nutritional virulence determinant with lipase activity important for Borrelia burgdorferi infection and survival in fatty acid deficient environments.BB0562 是一种具有脂肪酶活性的营养毒力决定因子,对于伯氏疏螺旋体感染和在脂肪酸缺乏环境中的生存至关重要。
PLoS Pathog. 2021 Aug 20;17(8):e1009869. doi: 10.1371/journal.ppat.1009869. eCollection 2021 Aug.
4
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.
5
Estimating the Frequency of Lyme Disease Diagnoses, United States, 2010-2018.估计 2010-2018 年美国莱姆病诊断的频率。
Emerg Infect Dis. 2021 Feb;27(2):616-619. doi: 10.3201/eid2702.202731.
6
Gene Regulation and Transcriptomics.基因调控与转录组学。
Curr Issues Mol Biol. 2021;42:223-266. doi: 10.21775/cimb.042.223. Epub 2020 Dec 10.
7
Interactions Between Ticks and Lyme Disease Spirochetes.蜱虫与莱姆病螺旋体的相互作用。
Curr Issues Mol Biol. 2021;42:113-144. doi: 10.21775/cimb.042.113. Epub 2020 Dec 8.
8
DksA plays an essential role in regulating the virulence of Borrelia burgdorferi.DksA在调节伯氏疏螺旋体的毒力方面发挥着重要作用。
Mol Microbiol. 2020 Jul;114(1):172-183. doi: 10.1111/mmi.14504. Epub 2020 Apr 14.
9
The Lon-1 Protease Is Required by Borrelia burgdorferi To Infect the Mammalian Host.博氏疏螺旋体(Borrelia burgdorferi)的 Lon-1 蛋白酶对于感染哺乳动物宿主是必需的。
Infect Immun. 2020 May 20;88(6). doi: 10.1128/IAI.00951-19.
10
The Lon-2 protease of Borrelia burgdorferi is critical for infection in the mammalian host.伯氏疏螺旋体的 Lon-2 蛋白酶对哺乳动物宿主的感染至关重要。
Mol Microbiol. 2020 May;113(5):938-950. doi: 10.1111/mmi.14460. Epub 2020 Jan 23.

hypothetical protein BB0563 在动物感染伯氏疏螺旋体中的作用。

Role of the Hypothetical Protein BB0563 during Borrelia burgdorferi Infection in Animals.

机构信息

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

出版信息

Infect Immun. 2023 Mar 15;91(3):e0053922. doi: 10.1128/iai.00539-22. Epub 2023 Feb 6.

DOI:10.1128/iai.00539-22
PMID:36744894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10016080/
Abstract

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.

摘要

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。