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牛病原体丝状支原体丝状亚种SC中的无标记插入诱变:lppQ突变体的特征分析

Unmarked insertional mutagenesis in the bovine pathogen Mycoplasma mycoides subsp. mycoides SC: characterization of a lppQ mutant.

作者信息

Janis Carole, Bischof Daniela, Gourgues Géraldine, Frey Joachim, Blanchard Alain, Sirand-Pugnet Pascal

机构信息

Université Victor Segalen Bordeaux 2, UMR 1090, 71 avenue Edouard Bourlaux, F-33140 Villenave d'Ornon, France.

INRA, UMR 1090, 71 avenue Edouard Bourlaux, F-33140 Villenave d'Ornon, France.

出版信息

Microbiology (Reading). 2008 Aug;154(Pt 8):2427-2436. doi: 10.1099/mic.0.2008/017640-0.

Abstract

Mycoplasma mycoides subspecies mycoides small colony (SC) is the aetiologic agent of contagious bovine pleuropneumonia (CBPP), a respiratory disease causing important losses in cattle production. The publication of the genome sequence of M. mycoides subsp. mycoides SC should facilitate the identification of putative virulence factors. However, real progress in the study of molecular mechanisms of pathogenicity also requires efficient molecular tools for gene inactivation. In the present study, we have developed a transposon-based approach for the random mutagenesis of M. mycoides subsp. mycoides SC. A PCR-based screening assay enabled the characterization of several mutants with knockouts of genes potentially involved in pathogenicity. The initial transposon was further improved by combining it with the transposon gammadelta TnpR/res recombination system to allow the production of unmarked mutations. Using this approach, we isolated a mutant free of antibiotic-resistance genes, in which the gene encoding the main lipoprotein LppQ was disrupted. The mutant was found to express only residual amounts of the truncated N-terminal end of LppQ. This approach opens the way to study virulence factors and pathogen-host interactions of M. mycoides subsp. mycoides SC and to develop new, genetically defined vaccine strains.

摘要

丝状支原体丝状亚种小菌落型(SC)是牛传染性胸膜肺炎(CBPP)的病原体,这是一种给养牛业造成重大损失的呼吸道疾病。丝状支原体丝状亚种小菌落型基因组序列的公布应有助于鉴定潜在的毒力因子。然而,致病性分子机制研究的真正进展还需要有效的基因失活分子工具。在本研究中,我们开发了一种基于转座子的方法用于丝状支原体丝状亚种小菌落型的随机诱变。一种基于PCR的筛选测定法能够对几个可能参与致病性的基因敲除突变体进行表征。通过将初始转座子与转座子γδTnpR/res重组系统相结合,对其进行了进一步改进,以产生无标记突变。使用这种方法,我们分离出了一个不含抗生素抗性基因的突变体,其中编码主要脂蛋白LppQ的基因被破坏。发现该突变体仅表达截短的LppQ N末端的残留量。这种方法为研究丝状支原体丝状亚种小菌落型的毒力因子和病原体-宿主相互作用以及开发新的、基因定义明确的疫苗株开辟了道路。

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