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首页> 外文期刊>Journal of Clinical Microbiology >Evidence for recombination in the flagellin locus of Campylobacter jejuni: implications for the flagellin gene typing scheme.
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Evidence for recombination in the flagellin locus of Campylobacter jejuni: implications for the flagellin gene typing scheme.

机译:空肠弯曲杆菌鞭毛蛋白基因座中重组的证据:对鞭毛蛋白基因分型方案的影响。

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摘要

The flagellin subunit of the flagellar filament in Campylobacter jejuni is encoded by two highly homologous tandem genes, flaA and flaB. The flaA gene was sequenced in 18 strains of C. jejuni, including isolates from three outbreak groups. Sequences obtained were compared with flaA sequences available in the GenBank database, and all were analyzed for mosaic gene structure by using recently described statistical tests for detecting gene conversion among aligned sets of sequences. Strong evidence was found supporting recombination between flaA genes of different strains (i.e., intergenomic recombination). Intragenomic recombination between the flaA and flaB genes of C. jejuni TGH9011 was also demonstrated. Both mechanisms of recombination may act as a potential means by which pathogenic strains can generate increased antigenic diversity, so allowing them to escape the immunological responses of the host. Furthermore, demonstration of recombination within and between flagellin loci of natural strains suggests that flagellin gene typing (restriction fragment length polymorphism analysis of PCR-amplified flagellin genes) cannot be considered a stable method for long-term monitoring of pathogenic Campylobacter populations.
机译:空肠弯曲菌中鞭毛丝的鞭毛蛋白亚基由两个高度同源的串联基因flaA和flaB编码。 flaA基因在18个空肠弯曲杆菌菌株中测序,包括来自三个暴发组的分离株。将获得的序列与GenBank数据库中可用的flaA序列进行比较,并使用最近描述的统计测试来检测所有序列的序列之间的转化,从而对所有基因进行镶嵌基因结构分析。发现有力的证据支持不同菌株的flaA基因之间的重组(即基因组重组)。还证实了空肠弯曲杆菌TGH9011的flaA和flaB基因之间的整合重组。两种重组机制都可能是致病菌株可以产生增加的抗原多样性的潜在手段,因此使它们能够逃脱宿主的免疫应答。此外,天然菌株鞭毛蛋白基因座内和之间重组的证明表明,鞭毛蛋白基因分型(PCR扩增鞭毛蛋白基因的限制性片段长度多态性分析)不能被视为长期监测病原性弯曲杆菌种群的稳定方法。

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