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Unintentional Genomic Changes Endow Cupriavidus metallidurans with an Augmented Heavy-Metal Resistance

机译:无意的基因组改变赋予Cupriavidus Metallannans,具有增强重金属抗性

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摘要

For the past three decades, Cupriavidus metallidurans has been one of the major model organisms for bacterial tolerance to heavy metals. Its type strain CH34 contains at least 24 gene clusters distributed over four replicons, allowing for intricate and multilayered metal responses. To gain organic mercury resistance in CH34, broad-spectrum mer genes were introduced in a previous work via conjugation of the IncP-1β plasmid pTP6. However, we recently noted that this CH34-derived strain, MSR33, unexpectedly showed an increased resistance to other metals (i.e., Co2+, Ni2+, and Cd2+). To thoroughly investigate this phenomenon, we resequenced the entire genome of MSR33 and compared its DNA sequence and basal gene expression profile to those of its parental strain CH34. Genome comparison identified 11 insertions or deletions (INDELs) and nine single nucleotide polymorphisms (SNPs), whereas transcriptomic analysis displayed 107 differentially expressed genes. Sequence data implicated the transposition of IS1088 in higher Co2+ and Ni2+ resistances and altered gene expression, although the precise mechanisms of the augmented Cd2+ resistance in MSR33 remains elusive. Our work indicates that conjugation procedures involving large complex genomes and extensive mobilomes may pose a considerable risk toward the introduction of unwanted, undocumented genetic changes. Special efforts are needed for the applied use and further development of small nonconjugative broad-host plasmid vectors, ideally involving CRISPR-related and advanced biosynthetic technologies.
机译:在过去的三十年中,Cupriavidus Metallidurans是对重金属的细菌耐受性的主要模型生物之一。其型菌株CH34含有分布在四个复制子上的至少24个基因簇,允许复杂和多层金属反应。为了在CH34中获得有机汞抗性,通过Concp-1β质粒PTP6共轭在先前的工作中引入广谱MEL基因。然而,我们最近注意到该CH34衍生的菌株MSR33意外地显示出对其他金属的抗性增加(即CO 2 +,Ni2 +和CD2 +)。为了彻底研究这种现象,我们重新开始了MSR33的整个基因组,并将其DNA序列和基础基因表达谱与其亲本菌株CH34的全部基因组进行了比较。基因组比较鉴定了11个插入或缺失(吲哚)和九个单核苷酸多态性(SNP),而转录组分析显示107个差异表达基因。序列数据涉及较高CO2 +和Ni2 +电阻中的IS1088的转子和改变的基因表达,尽管MSR33中的增强CD2 +电阻的精确机制仍然难以捉摸。我们的作品表明,涉及大型复杂基因组和广泛移动的共轭程序可能对引入不希望的无证遗传变化来构成相当大的风险。应用的使用和进一步发展小型非协调性宽宿主质粒载体需要特殊努力,理想情况下涉及CRISPR相关和先进的生物合成技术。

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