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本文引用的文献

1
The bicarbonate transporter is essential for Bacillus anthracis lethality.碳酸氢盐转运蛋白对炭疽杆菌的致死性至关重要。
PLoS Pathog. 2008 Nov;4(11):e1000210. doi: 10.1371/journal.ppat.1000210. Epub 2008 Nov 21.
2
Cell physiology and protein secretion of Bacillus licheniformis compared to Bacillus subtilis.地衣芽孢杆菌与枯草芽孢杆菌的细胞生理学和蛋白质分泌比较。
J Mol Microbiol Biotechnol. 2009;16(1-2):53-68. doi: 10.1159/000142894. Epub 2008 Oct 29.
3
Identification of a surrogate marker for infection in the African green monkey model of inhalation anthrax.在吸入性炭疽的非洲绿猴模型中鉴定感染的替代标志物。
Infect Immun. 2008 Dec;76(12):5790-801. doi: 10.1128/IAI.00520-08. Epub 2008 Oct 13.
4
Characterization of Bacillus anthracis iron-regulated surface determinant (Isd) proteins containing NEAT domains.含有NEAT结构域的炭疽芽孢杆菌铁调节表面决定簇(Isd)蛋白的特性分析
Mol Microbiol. 2008 Nov;70(4):983-99. doi: 10.1111/j.1365-2958.2008.06460.x. Epub 2008 Sep 30.
5
The PlcR virulence regulon of Bacillus cereus.蜡样芽孢杆菌的PlcR毒力调节子。
PLoS One. 2008 Jul 30;3(7):e2793. doi: 10.1371/journal.pone.0002793.
6
Efficacy of oritavancin in a murine model of Bacillus anthracis spore inhalation anthrax.奥利万星在小鼠吸入炭疽芽孢杆菌孢子炭疽模型中的疗效。
Antimicrob Agents Chemother. 2008 Sep;52(9):3350-7. doi: 10.1128/AAC.00360-08. Epub 2008 Jul 7.
7
The ProteoMiner in the proteomic arena: a non-depleting tool for discovering low-abundance species.蛋白质组学领域中的ProteoMiner:一种用于发现低丰度物种的非消耗性工具。
J Proteomics. 2008 Aug 21;71(3):255-64. doi: 10.1016/j.jprot.2008.05.002. Epub 2008 Jun 20.
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Genotyping of Bacillus cereus strains by microarray-based resequencing.基于微阵列重测序的蜡样芽孢杆菌菌株基因分型
PLoS One. 2008 Jul 2;3(7):e2513. doi: 10.1371/journal.pone.0002513.
9
Conference report on public health and clinical guidelines for anthrax.关于炭疽的公共卫生与临床指南会议报告
Emerg Infect Dis. 2008 Apr;14(4):e1. doi: 10.3201/eid1404.070969.
10
Discovery of virulence factors of pathogenic bacteria.病原菌毒力因子的发现。
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用于炭疽芽孢杆菌感染的新型独特诊断生物标志物。

Novel and unique diagnostic biomarkers for Bacillus anthracis infection.

作者信息

Sela-Abramovich Sagit, Chitlaru Theodor, Gat Orit, Grosfeld Haim, Cohen Ofer, Shafferman Avigdor

机构信息

Department of Biochemistry and Molecular Genetics, Life Science Research Israel Ltd, 2 Ness-Ziona 74100, Israel.

出版信息

Appl Environ Microbiol. 2009 Oct;75(19):6157-67. doi: 10.1128/AEM.00766-09. Epub 2009 Jul 31.

DOI:10.1128/AEM.00766-09
PMID:19648366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2753070/
Abstract

A search for bacterium-specific biomarkers in peripheral blood following infection with Bacillus anthracis was carried out with rabbits, using a battery of specific antibodies generated by DNA vaccination against 10 preselected highly immunogenic bacterial antigens which were identified previously by a genomic/proteomic/serologic screen of the B. anthracis secretome. Detection of infection biomarkers in the circulation of infected rabbits could be achieved only after removal of highly abundant serum proteins by chromatography using a random-ligand affinity column. Besides the toxin component protective antigen, the following three secreted proteins were detected in the circulation of infected animals: the chaperone and protease HtrA (BA3660), an NlpC/P60 endopeptidase (BA1952), and a protein of unknown function harboring two SH3 (Src homology 3) domains (BA0796). The three proteins could be detected in plasma samples from infected animals exhibiting 10(3) to 10(5) CFU/ml blood and also in standard blood cultures at 3 to 6 h post-bacterial inoculation at a bacteremic level as low as 10(3) CFU/ml. Furthermore, the three biomarkers appear to be present only in the secretome of B. anthracis, not in those of the related pathogens B. thuringiensis and B. cereus. To the best of our knowledge, this is the first report of direct detection of B. anthracis-specific proteins, other than the toxin components, in the circulation of infected animals.

摘要

利用针对10种预先选定的高免疫原性细菌抗原通过DNA疫苗接种产生的一组特异性抗体,对感染炭疽芽孢杆菌的兔子外周血中的细菌特异性生物标志物进行了研究。这些抗原先前通过炭疽芽孢杆菌分泌蛋白组的基因组/蛋白质组/血清学筛选得以鉴定。只有在使用随机配体亲和柱通过色谱法去除高度丰富的血清蛋白后,才能在受感染兔子的循环系统中检测到感染生物标志物。除了毒素成分保护性抗原外,在受感染动物的循环系统中还检测到以下三种分泌蛋白:伴侣蛋白和蛋白酶HtrA(BA3660)、一种NlpC/P60内肽酶(BA1952)以及一种具有两个SH3(Src同源结构域3)结构域的功能未知蛋白(BA0796)。这三种蛋白可以在血液中细菌浓度为10³至10⁵CFU/ml的受感染动物的血浆样本中检测到,也可以在细菌接种后3至6小时、菌血症水平低至10³CFU/ml的标准血液培养物中检测到。此外,这三种生物标志物似乎仅存在于炭疽芽孢杆菌的分泌蛋白组中,而不存在于相关病原体苏云金芽孢杆菌和蜡样芽孢杆菌的分泌蛋白组中。据我们所知,这是首次在受感染动物的循环系统中直接检测到除毒素成分外的炭疽芽孢杆菌特异性蛋白的报告。