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李斯特菌复杂感染策略的生物技术应用。

Biotechnological applications of Listeria's sophisticated infection strategies.

机构信息

Institute for Medical Microbiology, Justus-Liebig University, Frankfurter strasse 107, D-35392 Giessen, Germany.

出版信息

Microb Biotechnol. 2008 Sep;1(5):361-72. doi: 10.1111/j.1751-7915.2008.00037.x. Epub 2008 Jun 9.

DOI:10.1111/j.1751-7915.2008.00037.x
PMID:21261856
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3815243/
Abstract

Listeria monocytogenes is a Gram-positive bacterium that is able to survive both in the environment and to invade and multiply within eukaryotic cells. Currently L. monocytogenes represents one of the most well-studied and characterized microorganisms in bacterial pathogenesis. A hallmark of L. monocytogenes virulence is its ability to breach bodily barriers such as the intestinal epithelium, the blood-brain barrier as well as the placental barrier to cause severe systemic disease. Curiously, this theme is repeated at the level of the interaction between the individual cell and the bacterium where its virulence factors contribute to the ability of the bacteria to breach cellular barriers. L. monocytogenes is a model to study metabolic requirements of bacteria growing in an intracellular environment, modulation of signalling pathways in the infected cell and interactions with cellular defences involving innate and adaptive immunity. Technical advances such as the creation of LISTERIA-susceptible mouse strains, had added interest in the study of the natural pathogenesis of the disease via oral infection. The use of attenuated strains of L. monocytogenes as vaccines has gained considerable interest because they can be used to express heterologous antigens as well as to somatically deliver recombinant DNA to eukaryotic cells. A novel vaccine concept, the use of non-viable but metabolically active bacteria to induced immunoprotective responses, has been developed with L. monocytogenes. In this mini-review, we review the strategies used by L. monocytogenes to subvert the cellular functions at different stages of the infection cycle in the host and examine how these properties are being exploited in biotechnological and clinical applications.

摘要

李斯特菌是一种革兰氏阳性细菌,能够在环境中生存,并侵入和在真核细胞内繁殖。目前,李斯特菌是细菌发病机制中研究和描述最充分的微生物之一。李斯特菌的毒力标志之一是其能够突破身体屏障,如肠道上皮、血脑屏障和胎盘屏障,导致严重的全身疾病。奇怪的是,这一主题在个体细胞与细菌之间的相互作用中得到了重复,其毒力因子有助于细菌突破细胞屏障的能力。李斯特菌是研究在细胞内环境中生长的细菌代谢需求、感染细胞中信号通路的调节以及涉及固有和适应性免疫的细胞防御相互作用的模型。技术进步,如创建易受李斯特菌感染的小鼠品系,增加了通过口服感染研究疾病自然发病机制的兴趣。使用李斯特菌减毒株作为疫苗引起了相当大的兴趣,因为它们可以用来表达异源抗原,以及将重组 DNA体细胞传递给真核细胞。利用非存活但代谢活跃的细菌来诱导免疫保护反应的新型疫苗概念已经在李斯特菌中得到了发展。在这篇迷你综述中,我们回顾了李斯特菌在宿主感染周期的不同阶段颠覆细胞功能的策略,并探讨了这些特性如何在生物技术和临床应用中得到利用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5482/3815243/917db7871783/mbt0001-0361-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5482/3815243/6916b0d82c95/mbt0001-0361-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5482/3815243/917db7871783/mbt0001-0361-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5482/3815243/6916b0d82c95/mbt0001-0361-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5482/3815243/917db7871783/mbt0001-0361-f2.jpg

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本文引用的文献

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Novel bacterial artificial chromosome vector pUvBBAC for use in studies of the functional genomics of Listeria spp.用于李斯特菌属功能基因组学研究的新型细菌人工染色体载体pUvBBAC
Appl Environ Microbiol. 2008 Mar;74(6):1892-901. doi: 10.1128/AEM.00415-07. Epub 2008 Jan 25.
2
Listeriolysin O allows Listeria monocytogenes replication in macrophage vacuoles.溶血素O可使单核细胞增生李斯特菌在巨噬细胞液泡中复制。
Nature. 2008 Jan 17;451(7176):350-4. doi: 10.1038/nature06479.
3
Induction of suicidal erythrocyte death by listeriolysin from Listeria monocytogenes.
Microb Biotechnol. 2008 Nov;1(6):443-5. doi: 10.1111/j.1751-7915.2008.00068.x.
单核细胞增生李斯特菌的李斯特菌溶素诱导红细胞自杀性死亡。
Cell Physiol Biochem. 2007;20(6):1051-60. doi: 10.1159/000110715. Epub 2007 Oct 30.
4
Cdc42 and phosphoinositide 3-kinase drive Rac-mediated actin polymerization downstream of c-Met in distinct and common pathways.Cdc42和磷酸肌醇3激酶在不同且共同的途径中驱动c-Met下游的Rac介导的肌动蛋白聚合。
Mol Cell Biol. 2007 Oct;27(19):6615-28. doi: 10.1128/MCB.00367-07. Epub 2007 Aug 6.
5
Extending the host range of Listeria monocytogenes by rational protein design.通过合理的蛋白质设计扩展单核细胞增生李斯特菌的宿主范围。
Cell. 2007 Jun 1;129(5):891-902. doi: 10.1016/j.cell.2007.03.049.
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Sci Prog. 2007;90(Pt 1):1-14. doi: 10.3184/003685007780440530.
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Differential function of Listeria monocytogenes listeriolysin O and phospholipases C in vacuolar dissolution following cell-to-cell spread.单核细胞增生李斯特菌溶血素O和磷脂酶C在细胞间传播后液泡溶解中的差异功能。
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Autophagy limits Listeria monocytogenes intracellular growth in the early phase of primary infection.自噬在原发性感染的早期阶段限制了单核细胞增生李斯特菌的细胞内生长。
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