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攻克衣原体:难治性细胞内病原体基因操作的进展

Emancipating Chlamydia: Advances in the Genetic Manipulation of a Recalcitrant Intracellular Pathogen.

作者信息

Bastidas Robert J, Valdivia Raphael H

机构信息

Department of Molecular Genetics and Microbiology and Center for the Genomics of Microbial Systems, Duke University Medical Center, Durham, North Carolina, USA.

Department of Molecular Genetics and Microbiology and Center for the Genomics of Microbial Systems, Duke University Medical Center, Durham, North Carolina, USA

出版信息

Microbiol Mol Biol Rev. 2016 Mar 30;80(2):411-27. doi: 10.1128/MMBR.00071-15. Print 2016 Jun.

DOI:10.1128/MMBR.00071-15
PMID:27030552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4867370/
Abstract

Chlamydia species infect millions of individuals worldwide and are important etiological agents of sexually transmitted disease, infertility, and blinding trachoma. Historically, the genetic intractability of this intracellular pathogen has hindered the molecular dissection of virulence factors contributing to its pathogenesis. The obligate intracellular life cycle of Chlamydia and restrictions on the use of antibiotics as selectable markers have impeded the development of molecular tools to genetically manipulate these pathogens. However, recent developments in the field have resulted in significant gains in our ability to alter the genome of Chlamydia, which will expedite the elucidation of virulence mechanisms. In this review, we discuss the challenges affecting the development of molecular genetic tools for Chlamydia and the work that laid the foundation for recent advancements in the genetic analysis of this recalcitrant pathogen.

摘要

衣原体在全球感染了数百万人,是性传播疾病、不孕症和致盲性沙眼的重要病原体。从历史上看,这种细胞内病原体的基因难操作性阻碍了对其致病机制中致病因子的分子剖析。衣原体专性细胞内生命周期以及抗生素作为选择标记使用的限制,阻碍了对这些病原体进行基因操作的分子工具的开发。然而,该领域最近的进展使我们改变衣原体基因组的能力有了显著提高,这将加速对致病机制的阐明。在这篇综述中,我们讨论了影响衣原体分子遗传工具开发的挑战,以及为这种顽固病原体的遗传分析最近取得的进展奠定基础的工作。

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本文引用的文献

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Use of aminoglycoside 3' adenyltransferase as a selection marker for Chlamydia trachomatis intron-mutagenesis and in vivo intron stability.使用氨基糖苷3'腺苷转移酶作为沙眼衣原体内含子诱变和体内内含子稳定性的选择标记。
BMC Res Notes. 2015 Oct 15;8:570. doi: 10.1186/s13104-015-1542-9.
2
Expression and localization of predicted inclusion membrane proteins in Chlamydia trachomatis.沙眼衣原体中预测的包涵体膜蛋白的表达与定位
Infect Immun. 2015 Dec;83(12):4710-8. doi: 10.1128/IAI.01075-15. Epub 2015 Sep 28.
3
The Rsb Phosphoregulatory Network Controls Availability of the Primary Sigma Factor in Chlamydia trachomatis and Influences the Kinetics of Growth and Development.Rsb磷酸化调控网络控制沙眼衣原体主要σ因子的可用性,并影响其生长和发育动力学。
PLoS Pathog. 2015 Aug 27;11(8):e1005125. doi: 10.1371/journal.ppat.1005125. eCollection 2015 Aug.
4
Application of β-lactamase reporter fusions as an indicator of effector protein secretion during infections with the obligate intracellular pathogen Chlamydia trachomatis.β-内酰胺酶报告基因融合体作为专性胞内病原体沙眼衣原体感染期间效应蛋白分泌指标的应用。
PLoS One. 2015 Aug 10;10(8):e0135295. doi: 10.1371/journal.pone.0135295. eCollection 2015.
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Global Mapping of the Inc-Human Interactome Reveals that Retromer Restricts Chlamydia Infection.Inc-人类相互作用组的全球图谱揭示了回收体限制衣原体感染。
Cell Host Microbe. 2015 Jul 8;18(1):109-21. doi: 10.1016/j.chom.2015.06.004. Epub 2015 Jun 25.
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Cell Host Microbe. 2015 May 13;17(5):716-25. doi: 10.1016/j.chom.2015.03.014. Epub 2015 Apr 23.
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Novel Chlamydia trachomatis strains in heterosexual sex partners, Indianapolis, Indiana, USA.美国印第安纳州印第安纳波利斯市异性恋伴侣中的新型沙眼衣原体菌株。
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