Experimental evolution reveals the genetic basis and systems biology of superoxide stress tolerance

Author:

Tan Justin,Olson Connor A.,Park Joon Ho,Sastry Anand V.,Phaneuf Patrick V.,Yang Laurence,Szubin Richard,Hefner Ying,Feist Adam M.,Palsson Bernhard O.

Abstract

AbstractBacterial response to oxidative stress is of fundamental importance. Oxidative stresses are endogenous, such as reactive oxidative species (ROS) production during respiration, or exogenous in industrial biotechnology, due to culture conditions or product toxicity. The immune system inflicts strong ROS stress on invading pathogens. In this study we make use of Adaptive Laboratory Evolution (ALE) to generate two independent lineages ofEscherichia coliwith increased tolerance to superoxide stress by up to 500% compared to wild type. We found: 1) that the use of ALE reveals the genetic basis for and systems biology of ROS tolerance, 2) that there are only 6 and 7 mutations, respectively, in each lineage, five of which reproducibly occurred in the same genes (iron-sulfur cluster regulatoriscR, putative iron-sulfur repair proteinygfZ, pyruvate dehydrogenase subunit EaceE, succinate dehydrogenasesucA, and glutamine tRNAglnX), and 3) that the transcriptome of the strain lineages exhibits two different routes of tolerance: the direct mitigation and repair of ROS damage and the up-regulation of cell motility and swarming genes mediated through phosphate starvation, which has been linked to biofilm formation and aggregation. These two transcriptomic responses can be interpreted as ‘flight’ and ‘fight’ phenotypes.ImportanceBacteria encounter oxidative stress from multiple sources. During pathogenic infections, our body’s immune system releases ROS as a form of antimicrobial defense whilst bacteria used in industrial biotechnology are frequently exposed to genetic modifications and culture conditions which induce oxidative stress. In order to get around the body’s defences, pathogens have developed various adaptations to tolerate high levels of ROS, and these adaptive mechanisms are not always well understood. At the same time, there is a need to improve oxidative stress tolerance for industrially relevant strains in order to increase robustness and productivity. In this study we generate two strains of superoxide tolerantEscherichia coliand identify several adaptive mechanisms. These findings can be directly applied to improve production strain fitness in an industrial setting. They also provide insight into potential virulence factors in other pathogens, highlighting potential targets for antimicrobial compounds.

Publisher

Cold Spring Harbor Laboratory

Reference66 articles.

1. Anders, Simon , P. T. Pyl , and W. Huber . 2010. “HTSeq: Analysing High-Throughput Sequencing Data with Python.”

2. Making DNA without Iron--Induction of a Manganese-Dependent Ribonucleotide Reductase in Response to Iron Starvation;Molecular Microbiology,2011

3. Fe-S Cluster Assembly Pathways in Bacteria;Microbiology and Molecular Biology Reviews: MMBR,2008

4. Construction of Escherichia coli K‐12 in‐frame, single‐gene knockout mutants: the Keio collection

5. Escherichia Coli Avoids High Dissolved Oxygen Stress by Activation of SoxRS and Manganese-Superoxide Dismutase;Microbial Cell Factories,2013

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3