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

机译:无标记的插入诱变在牛病原体支原体mycoptes subsp中。 Mycoides SC:LPPQ突变体的表征

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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 γδ 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.
机译:mycoplasma mycoides亚种Mycoides小殖民地(SC)是传染牛胸膜炎(CBPP)的Aetiologic代理,一种呼吸系统疾病导致牛生产中的重要损失。发布M. mycoides subsp的基因组序列。 Mycoides SC应促进识别推定的毒力因子。然而,致病性分子机制研究的实际进展也需要有效的分子工具进行基因失活。在本研究中,我们开发了一种基于转座子的方法,用于对M. mycoides subsp的随机诱变。 mycoides sc。基于PCR的筛选测定使得几个突变体的表征具有潜在涉及致病性的基因的敲除。通过将其与转座γδTNPR/ res重组系统组合以允许生产未标记的突变来进一步改善初始转座子。使用这种方法,我们分离出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。发现突变体仅表达LPPQ截短的N-末端的残留量。这种方法打开了研究毒力因子和M. mycoides subsp的毒力因子和病原体相互作用的方法。 Mycoides SC并开发新的遗传定义疫苗菌株。

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