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测试多拷贝质粒在抗生素耐药性进化中的作用。

Testing the Role of Multicopy Plasmids in the Evolution of Antibiotic Resistance.

作者信息

Escudero Jose Antonio, MacLean R Craig, San Millan Alvaro

机构信息

Department of Animal Health, Universidad Complutense de Madrid.

Visavet Health Surveillance Centre, Universidad Complutense de Madrid.

出版信息

J Vis Exp. 2018 May 2(135):57386. doi: 10.3791/57386.

Abstract

Multicopy plasmids are extremely abundant in prokaryotes but their role in bacterial evolution remains poorly understood. We recently showed that the increase in gene copy number per cell provided by multicopy plasmids could accelerate the evolution of plasmid-encoded genes. In this work, we present an experimental system to test the ability of multicopy plasmids to promote gene evolution. Using simple molecular biology methods, we constructed a model system where an antibiotic resistance gene can be inserted into Escherichia coli MG1655, either in the chromosome or on a multicopy plasmid. We use an experimental evolution approach to propagate the different strains under increasing concentrations of antibiotics and we measure survival of bacterial populations over time. The choice of the antibiotic molecule and the resistance gene is so that the gene can only confer resistance through the acquisition of mutations. This "evolutionary rescue" approach provides a simple method to test the potential of multicopy plasmids to promote the acquisition of antibiotic resistance. In the next step of the experimental system, the molecular bases of antibiotic resistance are characterized. To identify mutations responsible for the acquisition of antibiotic resistance we use deep DNA sequencing of samples obtained from whole populations and clones. Finally, to confirm the role of the mutations in the gene under study, we reconstruct them in the parental background and test the resistance phenotype of the resulting strains.

摘要

多拷贝质粒在原核生物中极为丰富,但其在细菌进化中的作用仍知之甚少。我们最近表明,多拷贝质粒提供的每个细胞基因拷贝数增加可加速质粒编码基因的进化。在这项工作中,我们提出了一个实验系统来测试多拷贝质粒促进基因进化的能力。使用简单的分子生物学方法,我们构建了一个模型系统,其中抗生素抗性基因可以插入大肠杆菌MG1655的染色体或多拷贝质粒上。我们使用实验进化方法在不断增加的抗生素浓度下繁殖不同的菌株,并测量细菌群体随时间的存活率。抗生素分子和抗性基因的选择使得该基因只能通过获得突变来赋予抗性。这种“进化拯救”方法提供了一种简单的方法来测试多拷贝质粒促进获得抗生素抗性的潜力。在实验系统的下一步中,对抗生素抗性的分子基础进行表征。为了鉴定导致获得抗生素抗性的突变,我们对从整个群体和克隆中获得的样本进行深度DNA测序。最后,为了确认所研究基因中突变的作用,我们在亲本背景中重建它们并测试所得菌株的抗性表型。

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