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构建用于无乳支原体基因克隆和同源重组的首个穿梭载体。

Construction of the first shuttle vectors for gene cloning and homologous recombination in Mycoplasma agalactiae.

作者信息

Chopra-Dewasthaly Rohini, Marenda Marc, Rosengarten Renate, Jechlinger Wolfgang, Citti Christine

机构信息

Institute of Bacteriology, Mycology and Hygiene, Department of Pathobiology, University of Veterinary Medicine Vienna, Veterinärplatz 1, A-1210 Vienna, Austria.

出版信息

FEMS Microbiol Lett. 2005 Dec 1;253(1):89-94. doi: 10.1016/j.femsle.2005.09.021. Epub 2005 Sep 28.

Abstract

Mycoplasma agalactiae is a worldwide ruminant pathogen that causes significant economic losses by inflicting contagious agalactia in sheep and goats. The development of efficient control strategies requires a better understanding of the mycoplasma factors that promote successful infection. However, lack of genetic tools has been a major impediment in studying the pathogenic mechanisms of M. agalactiae. This study describes the identification and cloning of the M. agalactiae origin of replication (oriC) in order to construct the first shuttle vectors for targeted gene disruption, gene complementation and expression studies. Additionally, this report provides the first evidence of the occurrence of homologous recombination and the functionality of heterologous tetM determinant in this pathogen.

摘要

无乳支原体是一种全球范围内的反刍动物病原体,通过在绵羊和山羊中引发传染性无乳症而造成重大经济损失。制定有效的控制策略需要更好地了解促进成功感染的支原体因子。然而,缺乏遗传工具一直是研究无乳支原体致病机制的主要障碍。本研究描述了无乳支原体复制起点(oriC)的鉴定和克隆,以便构建首个用于靶向基因破坏、基因互补和表达研究的穿梭载体。此外,本报告首次提供了该病原体中发生同源重组以及异源tetM决定簇功能的证据。

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