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钩端螺旋体属基因替换的首个证据。双曲钩端螺旋体flaB的失活导致缺乏内鞭毛的无运动能力突变体。

First evidence for gene replacement in Leptospira spp. Inactivation of L. biflexa flaB results in non-motile mutants deficient in endoflagella.

作者信息

Picardeau M, Brenot A, Saint Girons I

机构信息

Unité de Bactériologie Moléculaire et Médicale, Institut Pasteur, 28 rue du docteur Roux, 75724 Paris Cedex 15, France.

出版信息

Mol Microbiol. 2001 Apr;40(1):189-99. doi: 10.1046/j.1365-2958.2001.02374.x.

Abstract

Leptospira spp. offer many advantages as model bacteria for the study of spirochaetes. However, homologous recombination between introduced DNA and the corresponding chromosomal loci has never been demonstrated. A unique feature of spirochaetes is the presence of endoflagella between the outer membrane sheath and the cell cylinder. We chose the flaB flagellin gene, constituting the flagellar core, as a target for gene inactivation in the saprophyte Leptospira biflexa. The amino acid sequence of the FlaB protein of L. biflexa was most similar to those of spirochaetes Brachyspira hyodysenteriae (agent of swine dysentery), Leptospira interrogans (agent of leptospirosis) and Treponema pallidum (agent of syphilis). A suicide vector containing the L. biflexa flaB gene disrupted by a kanamycin marker was UV irradiated or alkali denatured before electroporation. This methodology allowed the selection of many kanamycin-resistant colonies resulting from single and double cross-over events at the flaB locus. The double recombinant mutants are non-motile, as visualized in both liquid and semi-solid media. In addition, a flaB mutant selected for further analysis was shown to be deficient in endoflagella by electron microscopy. However, most of the transformants had resulted from a single homologous recombination event, giving rise to the integration of the suicide vector. We evaluated the effect of the sacB and rpsL genes in L. biflexa as potential counterselectable markers for allelic exchange, and then used the rpsL system for the positive selection of flaB double recombinants in a streptomycin-resistant strain. Like the flaB mutant studied above, the Strr double cross-over mutant was non-motile and deficient in endoflagella. Our results demonstrate that FlaB is involved in flagella assembly and motility. They also show the feasibility of performing allelic replacement in Leptospira spp. by homologous recombination.

摘要

钩端螺旋体属作为研究螺旋体的模式细菌具有诸多优势。然而,导入的DNA与相应染色体位点之间的同源重组从未得到证实。螺旋体的一个独特特征是在外膜鞘和细胞圆柱体之间存在内鞭毛。我们选择构成鞭毛核心的flaB鞭毛蛋白基因作为腐生双曲钩端螺旋体基因失活的靶点。双曲钩端螺旋体FlaB蛋白的氨基酸序列与猪痢疾密螺旋体(猪痢疾病原体)、问号钩端螺旋体(钩端螺旋体病病原体)和梅毒螺旋体(梅毒病原体)的最为相似。一个含有被卡那霉素标记破坏的双曲钩端螺旋体flaB基因的自杀载体在电穿孔前进行紫外线照射或碱变性处理。这种方法能够筛选出许多由flaB位点的单交换和双交换事件产生的卡那霉素抗性菌落。双重组突变体在液体和半固体培养基中均无运动能力。此外,通过电子显微镜观察,一个被选用于进一步分析的flaB突变体显示缺乏内鞭毛。然而,大多数转化体是由单个同源重组事件产生的,导致自杀载体的整合。我们评估了双曲钩端螺旋体中sacB和rpsL基因作为等位基因交换潜在反选择标记的作用,然后使用rpsL系统在链霉素抗性菌株中对flaB双重组体进行阳性筛选。与上述研究的flaB突变体一样,Strr双交换突变体无运动能力且缺乏内鞭毛。我们的结果表明FlaB参与鞭毛组装和运动。它们还显示了通过同源重组在钩端螺旋体属中进行等位基因置换的可行性。

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