• 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

……的差异生长改变了毒力因子、主要抗原和表面碳水化合物合酶的表达,决定了SchuS4对免疫动物的表观毒力。 (注:原文中“Differential Growth of ”后面缺少具体内容)

Differential Growth of , Which Alters Expression of Virulence Factors, Dominant Antigens, and Surface-Carbohydrate Synthases, Governs the Apparent Virulence of SchuS4 to Immunized Animals.

作者信息

Holland Kristen M, Rosa Sarah J, Kristjansdottir Kolbrun, Wolfgeher Donald, Franz Brian J, Zarrella Tiffany M, Kumar Sudeep, Sunagar Raju, Singh Anju, Bakshi Chandra S, Namjoshi Prachi, Barry Eileen M, Sellati Timothy J, Kron Stephen J, Gosselin Edmund J, Reed Douglas S, Hazlett Karsten R O

机构信息

Department of Immunology and Microbial Disease, Albany Medical CollegeAlbany, NY, United States.

Department of Biomedical Sciences, Midwestern UniversityDowners Grove, IL, United States.

出版信息

Front Microbiol. 2017 Jun 22;8:1158. doi: 10.3389/fmicb.2017.01158. eCollection 2017.

DOI:10.3389/fmicb.2017.01158
PMID:28690600
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5479911/
Abstract

The gram-negative bacterium () is both a potential biological weapon and a naturally occurring microbe that survives in arthropods, fresh water amoeba, and mammals with distinct phenotypes in various environments. Previously, we used a number of measurements to characterize grown in Brain-Heart Infusion (BHI) broth as (1) more similar to infection-derived bacteria, and (2) slightly more virulent in naïve animals, compared to grown in Mueller Hinton Broth (MHB). In these studies we observed that the free amino acids in MHB repress expression of select virulence factors by an unknown mechanism. Here, we tested the hypotheses that grown in BHI (BHI-) accurately displays a full protein composition more similar to that reported for infection-derived and that this similarity would make BHI- more susceptible to pre-existing, vaccine-induced immunity than MHB-. We performed comprehensive proteomic analysis of grown in MHB, BHI, and BHI supplemented with casamino acids (BCA) and compared our findings to published "omics" data derived from grown . Based on the abundance of ~1,000 proteins, the fingerprint of BHI- is one of nutrient-deprived bacteria that-through induction of a stringent-starvation-like response-have induced the FevR regulon for expression of the bacterium's virulence factors, immuno-dominant antigens, and surface-carbohydrate synthases. To test the notion that increased abundance of dominant antigens expressed by BHI- would render these bacteria more susceptible to pre-existing, vaccine-induced immunity, we employed a battery of LVS-vaccination and S4-challenge protocols using MHB- and BHI-grown S4. Contrary to our hypothesis, these experiments reveal that LVS-immunization provides a barrier to infection that is significantly more effective against an MHB-S4 challenge than a BHI-S4 challenge. The differences in apparent virulence to immunized mice are profoundly greater than those observed with primary infection of naïve mice. Our findings suggest that tularemia vaccination studies should be critically evaluated in regard to the growth conditions of the challenge agent.

摘要

革兰氏阴性细菌()既是一种潜在的生物武器,也是一种天然存在的微生物,它能在节肢动物、淡水变形虫和哺乳动物中生存,并在各种环境中呈现出不同的表型。此前,我们通过一系列测量来表征在脑心浸液(BHI)肉汤中培养的,结果表明:(1)与感染来源的细菌更相似;(2)与在米勒-欣顿肉汤(MHB)中培养的相比,在未接触过病原体的动物中,其毒性略强。在这些研究中,我们观察到MHB中的游离氨基酸通过未知机制抑制了某些毒力因子的表达。在此,我们检验了以下假设:在BHI(BHI-)中培养的能准确呈现出更类似于感染来源的完整蛋白质组成,并且这种相似性会使BHI-比MHB-更容易受到预先存在的疫苗诱导免疫的影响。我们对在MHB、BHI和添加了酪蛋白氨基酸的BHI(BCA)中培养的进行了全面的蛋白质组学分析,并将我们的研究结果与从培养的中获得的已发表的“组学”数据进行了比较。基于约1000种蛋白质的丰度,BHI-的指纹图谱显示其为营养缺乏型细菌,通过诱导一种类似严格饥饿的反应,诱导了FevR调控子来表达细菌的毒力因子、免疫显性抗原和表面碳水化合物合成酶。为了验证BHI-表达的显性抗原丰度增加会使这些细菌更容易受到预先存在的疫苗诱导免疫影响这一观点,我们采用了一系列使用MHB-和BHI-培养的S4进行的兔热病疫苗接种和S4攻击方案。与我们的假设相反,这些实验表明,兔热病疫苗接种提供了一道感染屏障,对MHB-S4攻击的防护效果明显比对BHI-S4攻击更有效。对免疫小鼠的明显毒力差异远大于对未接触过病原体的小鼠进行初次感染时观察到的差异。我们的研究结果表明,关于兔热病疫苗接种的研究应根据攻击病原体的生长条件进行严格评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/47f3f2cd9e89/fmicb-08-01158-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/ecf0a270ae40/fmicb-08-01158-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/782e3f1f686b/fmicb-08-01158-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/5ff8b9f30afa/fmicb-08-01158-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/757d6d380b17/fmicb-08-01158-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/73ab7d913aa0/fmicb-08-01158-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/47f3f2cd9e89/fmicb-08-01158-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/ecf0a270ae40/fmicb-08-01158-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/782e3f1f686b/fmicb-08-01158-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/5ff8b9f30afa/fmicb-08-01158-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/757d6d380b17/fmicb-08-01158-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/73ab7d913aa0/fmicb-08-01158-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/5479911/47f3f2cd9e89/fmicb-08-01158-g0006.jpg

相似文献

1
Differential Growth of , Which Alters Expression of Virulence Factors, Dominant Antigens, and Surface-Carbohydrate Synthases, Governs the Apparent Virulence of SchuS4 to Immunized Animals.……的差异生长改变了毒力因子、主要抗原和表面碳水化合物合酶的表达,决定了SchuS4对免疫动物的表观毒力。 (注:原文中“Differential Growth of ”后面缺少具体内容)
Front Microbiol. 2017 Jun 22;8:1158. doi: 10.3389/fmicb.2017.01158. eCollection 2017.
2
Adaptation of Francisella tularensis to the mammalian environment is governed by cues which can be mimicked in vitro.土拉弗朗西斯菌对哺乳动物环境的适应受可在体外模拟的信号所调控。
Infect Immun. 2008 Oct;76(10):4479-88. doi: 10.1128/IAI.00610-08. Epub 2008 Jul 21.
3
Growth conditions and environmental factors impact aerosolization but not virulence of Francisella tularensis infection in mice.生长条件和环境因素会影响土拉弗朗西斯菌感染的气溶胶化,但不会影响其毒力。
Front Cell Infect Microbiol. 2012 Oct 11;2:126. doi: 10.3389/fcimb.2012.00126. eCollection 2012.
4
Differential Cultivation of Induces Changes in the Immune Response to and Protective Efficacy of Whole Cell-Based Inactivated Vaccines.差异培养诱导对全细胞灭活疫苗的免疫反应和保护效力的变化。
Front Immunol. 2017 Jan 10;7:677. doi: 10.3389/fimmu.2016.00677. eCollection 2016.
5
Host-adaptation of Francisella tularensis alters the bacterium's surface-carbohydrates to hinder effectors of innate and adaptive immunity.土拉弗朗西斯菌的宿主适应性改变了细菌的表面碳水化合物,以阻碍先天和适应性免疫的效应物。
PLoS One. 2011;6(7):e22335. doi: 10.1371/journal.pone.0022335. Epub 2011 Jul 22.
6
Development, Characterization, and Standardization of a Nose-Only Inhalation Exposure System for Exposure of Rabbits to Small-Particle Aerosols Containing Francisella tularensis.开发、表征和标准化一种仅用于鼻腔吸入暴露系统,用于使兔子暴露于含有土拉弗朗西斯菌的小颗粒气溶胶中。
Infect Immun. 2019 Jul 23;87(8). doi: 10.1128/IAI.00198-19. Print 2019 Aug.
7
Preclinical testing of a vaccine candidate against tularemia.一种抗土拉菌病候选疫苗的临床前测试。
PLoS One. 2015 Apr 21;10(4):e0124326. doi: 10.1371/journal.pone.0124326. eCollection 2015.
8
Differential Cultivation of Influences Live Vaccine Protective Efficacy by Altering the Immune Response.差异培养通过改变免疫反应影响活疫苗的保护效力。
Front Immunol. 2018 Jul 10;9:1594. doi: 10.3389/fimmu.2018.01594. eCollection 2018.
9
Francisella tularensis Live Vaccine Strain deficient in capB and overexpressing the fusion protein of IglA, IglB, and IglC from the bfr promoter induces improved protection against F. tularensis respiratory challenge.缺失capB基因且从bfr启动子过表达IglA、IglB和IglC融合蛋白的土拉弗朗西斯菌活疫苗株可诱导对土拉弗朗西斯菌呼吸道攻击的更好保护。
Vaccine. 2016 Sep 22;34(41):4969-4978. doi: 10.1016/j.vaccine.2016.08.041. Epub 2016 Aug 28.
10
Vaccination evokes gender-dependent protection against tularemia infection in C57BL/6Tac mice.接种疫苗可在C57BL/6Tac小鼠中引发针对土拉菌病感染的性别依赖性保护作用。
Vaccine. 2016 Jun 17;34(29):3396-404. doi: 10.1016/j.vaccine.2016.04.054. Epub 2016 May 13.

引用本文的文献

1
Treatment of bacterial biothreat agents with a novel purified bioactive lactoferrin affects both growth and biofilm formation.用一种新型纯化生物活性乳铁蛋白治疗细菌生物威胁因子会影响其生长和生物膜形成。
Front Cell Infect Microbiol. 2025 Jun 17;15:1603689. doi: 10.3389/fcimb.2025.1603689. eCollection 2025.
2
Mutation of , a -formyltransferase involved in O-antigen synthesis, results in biofilm formation, phase variation and attenuation in .突变, 一种参与 O-抗原合成的甲酰基转移酶,导致生物膜形成、相变异和减弱 。
Microbiology (Reading). 2024 Feb;170(2). doi: 10.1099/mic.0.001437.
3
Diverse roles of low-molecular weight thiol GSH in 's virulence, location sensing and GSH-stealing from host.

本文引用的文献

1
Differential Cultivation of Induces Changes in the Immune Response to and Protective Efficacy of Whole Cell-Based Inactivated Vaccines.差异培养诱导对全细胞灭活疫苗的免疫反应和保护效力的变化。
Front Immunol. 2017 Jan 10;7:677. doi: 10.3389/fimmu.2016.00677. eCollection 2016.
2
Inclusion of Epitopes That Expand High-Avidity CD4+ T Cells Transforms Subprotective Vaccines to Efficacious Immunogens against Virulent Francisella tularensis.包含可扩增高亲和力CD4+T细胞的表位可将亚保护性疫苗转化为针对强毒土拉弗朗西斯菌的有效免疫原。
J Immunol. 2016 Oct 1;197(7):2738-47. doi: 10.4049/jimmunol.1600879. Epub 2016 Aug 19.
3
低分子量硫醇谷胱甘肽(GSH)在[具体生物名称未给出]的毒力、位置感知及从宿主窃取GSH过程中的多种作用
Curr Res Microb Sci. 2023 Dec 20;6:100218. doi: 10.1016/j.crmicr.2023.100218. eCollection 2024.
4
Why vary what's working? Phase variation and biofilm formation in .为何要改变有效的方法?……中的相变和生物膜形成
Front Microbiol. 2022 Dec 6;13:1076694. doi: 10.3389/fmicb.2022.1076694. eCollection 2022.
5
Arginine Catabolism and Polyamine Biosynthesis Pathway Disparities Within Subpopulations.亚群内精氨酸分解代谢和多胺生物合成途径的差异
Front Microbiol. 2022 Jun 20;13:890856. doi: 10.3389/fmicb.2022.890856. eCollection 2022.
6
Phase Variation of LPS and Capsule Is Responsible for Stochastic Biofilm Formation in .脂多糖和荚膜的相变异导致 生物膜形成的随机性。
Front Cell Infect Microbiol. 2022 Jan 14;11:808550. doi: 10.3389/fcimb.2021.808550. eCollection 2021.
7
Development and Properties of Subsp. 15 NIIEG Vaccine Strain without the Gene.不含该基因的15 NIIEG亚种疫苗株的开发与特性
Vaccines (Basel). 2022 Jan 11;10(1):108. doi: 10.3390/vaccines10010108.
8
Development, Phenotypic Characterization and Genomic Analysis of a Panel for Tularemia Vaccine Testing.兔热病疫苗测试组的开发、表型特征分析及基因组分析
Front Microbiol. 2021 Aug 11;12:725776. doi: 10.3389/fmicb.2021.725776. eCollection 2021.
9
Early infection-induced natural antibody response.早期感染诱导的天然抗体反应。
Sci Rep. 2021 Jan 15;11(1):1541. doi: 10.1038/s41598-021-81083-0.
10
Virulence of Subspecies Biovar and Phenotypic Change during Serial Passages on Artificial Media.人工培养基连续传代过程中生物变种亚种的毒力及表型变化
Microorganisms. 2020 Nov 27;8(12):1881. doi: 10.3390/microorganisms8121881.
Evidence Suggesting That Francisella tularensis O-Antigen Capsule Contains a Lipid A-Like Molecule That Is Structurally Distinct from the More Abundant Free Lipid A.
有证据表明,土拉弗朗西斯菌O抗原荚膜含有一种类脂A分子,其结构与更丰富的游离脂A不同。
PLoS One. 2016 Jun 21;11(6):e0157842. doi: 10.1371/journal.pone.0157842. eCollection 2016.
4
Metabolic Reprogramming of Host Cells by Virulent Francisella tularensis for Optimal Replication and Modulation of Inflammation.强毒土拉弗朗西斯菌对宿主细胞的代谢重编程以实现最佳复制和炎症调节
J Immunol. 2016 May 15;196(10):4227-36. doi: 10.4049/jimmunol.1502456. Epub 2016 Mar 30.
5
The Divergent Intracellular Lifestyle of Francisella tularensis in Evolutionarily Distinct Host Cells.土拉弗朗西斯菌在进化上不同宿主细胞中的不同细胞内生活方式
PLoS Pathog. 2015 Dec 3;11(12):e1005208. doi: 10.1371/journal.ppat.1005208. eCollection 2015 Dec.
6
Characterization of Francisella tularensis Schu S4 mutants identified from a transposon library screened for O-antigen and capsule deficiencies.从经筛选的转座子文库中鉴定出的土拉弗朗西斯菌Schu S4突变体的特征,该文库筛选的是O抗原和荚膜缺陷。
Front Microbiol. 2015 May 5;6:338. doi: 10.3389/fmicb.2015.00338. eCollection 2015.
7
Ubiquitous promoter-localization of essential virulence regulators in Francisella tularensis.土拉弗朗西斯菌中必需毒力调节因子的普遍启动子定位
PLoS Pathog. 2015 Apr 1;11(4):e1004793. doi: 10.1371/journal.ppat.1004793. eCollection 2015 Apr.
8
Atomic structure of T6SS reveals interlaced array essential to function.VI型分泌系统的原子结构揭示了对功能至关重要的交错阵列。
Cell. 2015 Feb 26;160(5):940-951. doi: 10.1016/j.cell.2015.02.005.
9
Successful protection against tularemia in C57BL/6 mice is correlated with expansion of Francisella tularensis-specific effector T cells.在C57BL/6小鼠中成功预防土拉菌病与土拉热弗朗西斯菌特异性效应T细胞的扩增相关。
Clin Vaccine Immunol. 2015 Jan;22(1):119-28. doi: 10.1128/CVI.00648-14. Epub 2014 Nov 19.
10
Live attenuated Francisella novicida vaccine protects against Francisella tularensis pulmonary challenge in rats and non-human primates.减毒活新凶手弗朗西斯菌疫苗可保护大鼠和非人灵长类动物免受土拉弗朗西斯菌肺部攻击。
PLoS Pathog. 2014 Oct 23;10(10):e1004439. doi: 10.1371/journal.ppat.1004439. eCollection 2014 Oct.