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本文引用的文献

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Substituted diphenyl ethers as a broad-spectrum platform for the development of chemotherapeutics for the treatment of tularaemia.取代二苯醚作为治疗土拉菌病化疗药物的广谱平台。
J Antimicrob Chemother. 2009 Nov;64(5):1052-61. doi: 10.1093/jac/dkp307. Epub 2009 Sep 4.
2
Francisella tularensis induces ubiquitin-dependent major histocompatibility complex class II degradation in activated macrophages.土拉弗朗西斯菌在活化巨噬细胞中诱导泛素依赖性主要组织相容性复合体II类降解。
Infect Immun. 2009 Nov;77(11):4953-65. doi: 10.1128/IAI.00844-09. Epub 2009 Aug 24.
3
Contribution of citrulline ureidase to Francisella tularensis strain Schu S4 pathogenesis.瓜氨酸脲酶对土拉热弗朗西斯菌Schu S4菌株致病机制的作用。
J Bacteriol. 2009 Aug;191(15):4798-806. doi: 10.1128/JB.00212-09. Epub 2009 Jun 5.
4
Mucosal immunotherapy for protection from pneumonic infection with Francisella tularensis.用于预防土拉弗朗西斯菌肺炎感染的黏膜免疫疗法。
Vaccine. 2009 Jul 16;27(33):4424-33. doi: 10.1016/j.vaccine.2009.05.041. Epub 2009 May 31.
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Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources.利用DAVID生物信息学资源对大型基因列表进行系统和综合分析。
Nat Protoc. 2009;4(1):44-57. doi: 10.1038/nprot.2008.211.
6
Recombinant attenuated Listeria monocytogenes vaccine expressing Francisella tularensis IglC induces protection in mice against aerosolized Type A F. tularensis.表达土拉弗朗西斯菌IglC的重组减毒单核细胞增生李斯特菌疫苗可诱导小鼠对雾化A型土拉弗朗西斯菌产生保护作用。
Vaccine. 2009 Feb 18;27(8):1216-29. doi: 10.1016/j.vaccine.2008.12.014. Epub 2009 Jan 4.
7
Francisella tularensis regulates autophagy-related host cell signaling pathways.土拉弗朗西斯菌调节自噬相关的宿主细胞信号通路。
Autophagy. 2009 Jan;5(1):125-8. doi: 10.4161/auto.5.1.7305. Epub 2009 Jan 31.
8
Direct and indirect impairment of human dendritic cell function by virulent Francisella tularensis Schu S4.强毒土拉弗朗西斯菌Schu S4对人树突状细胞功能的直接和间接损害
Infect Immun. 2009 Jan;77(1):180-95. doi: 10.1128/IAI.00879-08. Epub 2008 Nov 3.
9
Immune response to Mycobacterium tuberculosis and identification of molecular markers of disease.对结核分枝杆菌的免疫反应及疾病分子标志物的鉴定。
Am J Respir Cell Mol Biol. 2009 Apr;40(4):398-409. doi: 10.1165/rcmb.2008-0248OC. Epub 2008 Sep 11.
10
Transcriptional profiling of a mice plague model: insights into interaction between Yersinia pestis and its host.小鼠鼠疫模型的转录谱分析:对鼠疫耶尔森菌与其宿主间相互作用的见解
J Basic Microbiol. 2009 Feb;49(1):92-9. doi: 10.1002/jobm.200800027.

鉴定感染强毒和弱毒兔热病弗朗西斯菌后小鼠体内独特免疫应答的遗传学特征。

Genetic identification of unique immunological responses in mice infected with virulent and attenuated Francisella tularensis.

机构信息

Rocky Mountain Regional Center of Excellence, Colorado State University, Fort Collins, CO 80523, USA.

出版信息

Microbes Infect. 2011 Mar;13(3):261-75. doi: 10.1016/j.micinf.2010.10.022. Epub 2010 Nov 9.

DOI:10.1016/j.micinf.2010.10.022
PMID:21070859
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3031720/
Abstract

Francisella tularensis is a category A select agent based on its infectivity and virulence but disease mechanisms in infection remain poorly understood. Murine pulmonary models of infection were therefore employed to assess and compare dissemination and pathology and to elucidate the host immune response to infection with the highly virulent Type A F. tularensis strain Schu4 versus the less virulent Type B live vaccine strain (LVS). We found that dissemination and pathology in the spleen was significantly greater in mice infected with F. tularensis Schu4 compared to mice infected with F. tularensis LVS. Using gene expression profiling to compare the response to infection with the two F. tularensis strains, we found that there were significant differences in the expression of genes involved in the apoptosis pathway, antigen processing and presentation pathways, and inflammatory response pathways in mice infected with Schu4 when compared to LVS. These transcriptional differences coincided with marked differences in dissemination and severity of organ lesions in mice infected with the Schu4 and LVS strains. Therefore, these findings indicate that altered apoptosis, antigen presentation and production of inflammatory mediators explain the differences in pathogenicity of F. tularensis Schu4 and LVS.

摘要

弗朗西斯菌是一种 A 类选择剂,这是基于其传染性和毒力,但感染的发病机制仍知之甚少。因此,采用了鼠类肺部感染模型来评估和比较传播和病理学,并阐明对高毒力 A 型弗朗西斯菌菌株 Schu4 与低毒力活疫苗菌株(LVS)感染的宿主免疫反应。我们发现,与感染 LVS 的小鼠相比,感染 F. tularensis Schu4 的小鼠脾脏中的传播和病理学显著增加。通过基因表达谱比较两种 F. tularensis 菌株的感染反应,我们发现感染 Schu4 的小鼠中,涉及凋亡途径、抗原加工和呈递途径以及炎症反应途径的基因表达存在显著差异,与 LVS 相比。这些转录差异与感染 Schu4 和 LVS 菌株的小鼠的传播和器官损伤严重程度的明显差异一致。因此,这些发现表明,凋亡、抗原呈递和炎症介质产生的改变解释了 F. tularensis Schu4 和 LVS 致病性的差异。