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

机译:意外的基因组变化赋予金属利尿铜核糖耐性增强,重金属抵抗力增强

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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., Co 2+ , Ni 2+ , and Cd 2+ ). 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 IS 1088 in higher Co 2+ and Ni 2+ resistances and altered gene expression, although the precise mechanisms of the augmented Cd 2+ 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,Cupidavid metallidurans一直是细菌对重金属的耐受性的主要模式生物之一。其类型菌株CH34包含分布在四个复制子上的至少24个基因簇,从而实现了复杂的多层金属响应。为了在CH34中获得对有机汞的抗性,在先前的工作中通过结合IncP-1β质粒pTP6引入了广谱mer基因。但是,我们最近注意到,这种源自CH34的菌株MSR33出乎意料地显示出对其他金属(即Co 2+,Ni 2+和Cd 2+)的抗性增强。为了彻底研究这种现象,我们对MSR33的整个基因组进行了重新测序,并将其DNA序列和基础基因表达谱与其亲本菌株CH34进行了比较。基因组比较确定了11个插入或缺失(INDEL)和9个单核苷酸多态性(SNP),而转录组分析显示了107个差异表达的基因。序列数据暗示IS 1088在较高的Co 2+和Ni 2+抗性中易位,并且基因表达发生了变化,尽管MSR33中增强的Cd 2+抗性的确切机制仍不清楚。我们的工作表明,涉及复杂的大型基因组和大量的运动信息组的偶联程序可能会对引入不需要的,无证的遗传变化带来巨大的风险。小型非缀合的宽宿主质粒载体的应用使用和进一步开发需要作出特殊的努力,理想地涉及CRISPR相关和先进的生物合成技术。

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