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Identification of a Genomic Island of Actinobacillus actinomycetemcomitans.

机译:放线放线杆菌基因组岛的鉴定。

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Background: Horizontal gene transfer (HGT) is a process by which bacteria acquire genes from organisms of distant taxa. HGT is now recognized as a major driving force in the evolution of bacterial pathogens. Through this process, bacteria may accumulate blocks of DNA such as genomic islands (GEIs) that encode fitness or virulence factors. The periodontal pathogen A. actinomycetemcomitans has been known to exhibit variable virulence potential. It is postulated that GEIs may play a role in modifying the virulence potential of A. actinomycetemcomitans. This study was initiated to identify and determine the distribution of GEIs in A. actinomycetemcomitans. Methods: Forty-seven A. actinomycetemcomitans strains of serotypes a through f were examined. Strain-specific variant DNA in the genomes of A. actinomycetemcomitans was identified by polymerase chain reaction (PCR) genomic mapping and sequenced to identify GEIs. The distribution of the GEIs among test strains of A. actinomycetemcomitans was determined byPCR analysis and Southern hybridization assays. Results: An approximately 22 kb GEI of A. actinomycetemcomitans, designated AAI-1, was identified in five serotype b strains. The AAI-1 exhibits low %G+C and encodes proteins of phage, restriction modification systems, mobile elements, and other hypothetical proteins of unknown functions. The insertion of AAI-1 was found to cause truncation of A. actinomycetemcomitans genes at the insertion site. Conclusions: Some A. actinomycetemcomitans strains may harbor GEIs, which were acquired via HGT by the bacteria. The GEIs may increase the gene repertoire of A. actinomycetemcomitans. However, the insertion of the GEIs in A. actinomycetemcomitans may also cause truncation and inactivation of resident genes at the insertion sites. The virulence significance of such gain and loss of genes in A. actinomycetemcomitans remains to be determined.
机译:背景:水平基因转移(HGT)是细菌从远处的生物分类中获取基因的过程。 HGT现在被认为是细菌病原体进化的主要驱动力。通过此过程,细菌可能会积聚DNA块,例如编码适应性或毒力因子的基因岛(GEI)。已知牙周病原体放线菌A.放线菌具有可变的毒力潜能。推测GEI可能在修饰放线放线杆菌的毒性潜能中起作用。开始这项研究以鉴定和确定GEI在放线放线杆菌中的分布。方法:检查了47个血清型a至f的放线放线杆菌。通过聚合酶链反应(PCR)基因组图谱鉴定放线放线杆菌基因组中的菌株特异性变异DNA,并进行测序以鉴定GEI。通过PCR分析和Southern杂交测定来确定GEIs在放线放线杆菌的测试菌株之间的分布。结果:在五种血清型b菌株中鉴定出大约22 kb的AEI放线放线杆菌的GEI。 AAI-1的%G + C含量低,并且可以编码噬菌体,限制性修饰系统,移动元件和其他功能未知的假设蛋白质。发现AAI-1的插入在插入位点引起放线放线杆菌基因的截短。结论:一些放线菌的菌株可能带有GEI,这些菌株是通过细菌通过HGT获得的。 GEIs可能会增加放线放线杆菌的基因库。但是,GEIs在放线放线菌中的插入也可能导致插入位点处的驻留基因被截断和失活。在放线放线杆菌中这种基因的获得和丢失的毒力意义仍有待确定。

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