Guidot Alice, Coupat Bénédicte, Fall Saliou, Prior Philippe, Bertolla Franck
CIRAD, UMR Peuplements Végétaux et Bioagresseurs en Milieu Tropical, Saint Pierre, La Réunion, France.
ISME J. 2009 May;3(5):549-62. doi: 10.1038/ismej.2009.14. Epub 2009 Feb 26.
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, II and III 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.
植物病原性β-变形菌茄科雷尔氏菌是一个复杂的物种,因为大多数菌株都具有自然可转化的共同特征。在本研究中,我们采用了一种基于微阵列比较基因组杂交(CGH)的新方法,来研究茄科雷尔氏菌不同菌株之间水平基因转移(HGTs)的程度。来自I、II和III型的受体菌株在体外被GMI1000参考菌株(I型)的基因组DNA自然转化,所得DNA与代表GMI1000菌株5120个预测基因的微阵列杂交。除了抗生素抗性标记的转移外,在16个测试转化体中的8个中,微阵列CGH检测到了其他转移的GMI1000基因,并揭示了它们的数量、类别、功能以及在基因组上的定位。我们发现,在单个事件中,长达30 kb的DNA片段和33个基因可以被整合。这些片段大多位于标记基因DNA的两侧,但有趣的是,在一次转化实验中,单个重组克隆中也沿着基因组发生了多次DNA获取。结果通过PCR扩增、克隆、测序和Southern印迹杂交得到了证实。这代表了在自然转化实验中首次对受体细菌菌株基因组上基因的获取和丢失进行全面鉴定。在未来的研究中,这种策略应有助于回答许多与HGT机制相关的问题。