首页> 外文期刊>The ISME journal emultidisciplinary journal of microbial ecology >Horizontal gene transfer between Ralstonia solanacearum strains detected by comparative genomic hybridization on microarrays
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Horizontal gene transfer between Ralstonia solanacearum strains detected by comparative genomic hybridization on microarrays

机译:基因芯片上比较基因组杂交检测青枯雷尔氏菌菌株之间的水平基因转移

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摘要

The plant pathogenic Betaproteobacterium Ralstonia solanacearum is a complex species in that most of the strains share the common characteristic of being naturally transformable. In this study, we used a new approach based on comparative genomic hybridization (CGH) on microarrays to investigate the extent of horizontal gene transfers (HGTs) between different strains of R. solanacearum. Recipient strains from phylotypes I, Il and Ill were naturally transformed in vitro by genomic DNA from the GMI1000 reference strain (phylotype I) and the resulting DNAs were hybridized on a microarray representative of the 5120 predicted genes from the GMI1000 strain. In addition to transfer of the antibiotic resistance marker, in 8 of the 16 tested transformants, CGH on microarrays detected other transferred GMI1000 genes and revealed their number, category, function and localization along the genome. We showed that DNA blocks up to 30 kb and 33 genes could be integrated during a single event. Most of these blocks flanked the marker gene DNA but, interestingly, multiple DNA acquisitions along the genome also occurred in a single recombinant clone in one transformation experiment. The results were confirmed by PCR amplification, cloning and sequencing and Southern blot hybridization. This represents the first comprehensive identification of gene acquisitions and losses along the genome of the recipient bacterial strain during natural transformation experiments. In future studies, this strategy should help to answer many questions related to HGT mechanisms.
机译:植物致病性β-变形杆菌Ralstonia solanacearum是一个复杂的物种,因为大多数菌株都具有可自然转化的共同特征。在这项研究中,我们在微阵列上使用了基于比较基因组杂交(CGH)的新方法来研究青枯菌不同菌株之间水平基因转移(HGT)的程度。通过来自GMI1000参考菌株(基因型I)的基因组DNA在体外天然转化了来自系统型I,II和III的受体菌株,并将得到的DNA在代表来自GMI1000菌株的5120个预测基因的微阵列上杂交。除了转移抗生素抗性标记外,在16个测试的转化子中的8个中,微阵列上的CGH还检测到其他转移的GMI1000基因,并揭示了它们的数量,类别,功能和在基因组中的定位。我们证明了单个事件中最多可以整合30 kb的DNA块和33个基因。这些块中的大多数位于标记基因DNA的两侧,但有趣的是,在一个转化实验中,单个重组克隆中也发生了沿基因组的多个DNA采集。 PCR扩增,克隆和测序以及Southern印迹杂交证实了结果。这代表在自然转化实验过程中,首次全面鉴定了受体细菌菌株基因组中的基因获取和损失。在以后的研究中,该策略应有助于回答许多与HGT机制有关的问题。

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