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Exploiting Adaptive Laboratory Evolution of Streptomyces clavuligerus for Antibiotic Discovery and Overproduction

机译:利用链霉菌链霉菌的自适应实验室进化来发现和过量生产抗生素

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摘要

Adaptation is normally viewed as the enemy of the antibiotic discovery and development process because adaptation among pathogens to antibiotic exposure leads to resistance. We present a method here that, in contrast, exploits the power of adaptation among antibiotic producers to accelerate the discovery of antibiotics. A competition-based adaptive laboratory evolution scheme is presented whereby an antibiotic-producing microorganism is competed against a target pathogen and serially passed over time until the producer evolves the ability to synthesize a chemical entity that inhibits growth of the pathogen. When multiple Streptomyces clavuligerus replicates were adaptively evolved against methicillin-resistant Staphylococcus aureus N315 in this manner, a strain emerged that acquired the ability to constitutively produce holomycin. In contrast, no holomycin could be detected from the unevolved wild-type strain. Moreover, genome re-sequencing revealed that the evolved strain had lost pSCL4, a large 1.8 Mbp plasmid, and acquired several single nucleotide polymorphisms in genes that have been shown to affect secondary metabolite biosynthesis. These results demonstrate that competition-based adaptive laboratory evolution can constitute a platform to create mutants that overproduce known antibiotics and possibly to discover new compounds as well.
机译:通常将适应视为抗生素发现和开发过程的敌人,因为病原体之间对抗生素暴露的适应会导致耐药性。相反,我们在这里提出一种方法,利用抗生素生产商之间的适应能力来加速抗生素的发现。提出了一种基于竞争的适应性实验室进化方案,在该方案中,生产抗生素的微生物与目标病原体竞争,并随着时间的流逝依次传播,直到生产者发展出合成抑制病原体生长的化学实体的能力。当以这种方式针对耐甲氧西林的金黄色葡萄球菌N315适应性进化多个棒状链霉菌复制品时,出现了一种菌株,该菌株获得了组成型生产全息霉素的能力。相反,从未进化的野生型菌株中未检测到全霉素。此外,基因组重测序显示进化的菌株丢失了pSCL4(一个1.8 Mbp的大质粒),并在基因中获得了几个单核苷酸多态性,这些基因已显示出会影响次级代谢产物的生物合成。这些结果表明,基于竞争的适应性实验室进化可以构成一个平台,以创建过量生产已知抗生素的突变体,并可能发现新化合物。

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