...
首页> 外文期刊>Journal of Clinical Microbiology >Molecular Analysis of Riboflavin Synthesis Genes in Bartonella henselae and Use of the ribCGene for Differentiation of Bartonella Species by PCR
【24h】

Molecular Analysis of Riboflavin Synthesis Genes in Bartonella henselae and Use of the ribCGene for Differentiation of Bartonella Species by PCR

机译:半夏巴尔通体核黄素合成基因的分子分析及ribC基因在PCR中鉴别巴尔通体的研究

获取原文

摘要

The biosynthesis pathway for riboflavin (vitamin B2), the precursor of the essential cofactors flavin mononucleotide and flavin adenine dinucleotide, is present in bacteria and plants but is absent in vertebrates. Due to their conservation in bacterial species and their absence in humans, the riboflavin synthesis genes should be well suited either for detection of bacterial DNA in human specimens or for the differentiation of pathogenic bacteria by molecular techniques. A DNA fragment carrying the genes ribD, ribC, and ribE, which encode homologues of riboflavin deaminase (RibD) and subunits of riboflavin synthetase (RibC and RibE), respectively, was isolated from a plasmid-based DNA library of the human pathogen Bartonella henselae by complementation of aribC mutation in Escherichia coli. Sequence analysis of the ribC gene region in strains of B. henselae, which were previously shown to be genetically different, revealed that the ribC gene is highly conserved at the species level. PCR amplification with primers derived from theribC locus of B. henselae was used to isolate the corresponding DNA regions in B. bacilliformis, B. clarridgeiae, and B. quintana. Sequence analysis indicated that the riboflavin synthesis genes are conserved and show the same operon-like genetic organization in all fourBartonella species. Primer oligonucleotides designed on the basis of localized differences within the ribC DNA region were successfully used to develop species-specific PCR assays for the differentiation of B. henselae, B. clarridgeiae, B. quintana, and B. bacilliformis. The results obtained indicate that the riboflavin synthesis genes are excellent targets for PCR-directed differentiation of these emerging pathogens. The PCR assays developed should increase our diagnostic potential to differentiate Bartonellaspecies, especially B. henselae and the newly recognized species B. clarridgeiae.
机译:细菌和植物中存在核黄素(维生素B 2 )(必需辅因子黄素单核苷酸和黄素腺嘌呤二核苷酸的前体)的生物合成途径,但在脊椎动物中却不存在。由于它们在细菌物种中的保守性以及在人类中的缺失,因此核黄素合成基因应该非常适合检测人类标本中的细菌DNA或通过分子技术区分病原细菌。带有基因 ribD ribC ribE 的DNA片段,其编码核黄素脱氨酶(RibD)和核黄素合成酶(RibC)的亚基和RibE)分别通过互补大肠杆菌中的 ribC 突变从人类病原体 Bartonella henselae 的基于质粒的DNA文库中分离>。 B菌株中 ribC 基因区域的序列分析。以前被证明在遗传上有所不同的henselae 揭示了 ribC 基因在物种水平上是高度保守的。用来源于 B的 ribC 基因座的引物进行PCR扩增。 henselae 用于分离 B中相应的DNA区域。芽孢杆菌 B。 clarridgeiae B。金塔纳州。序列分析表明核黄素合成基因是保守的,并且在所有四个 Bartonella 物种中显示出相同的操纵子样遗传组织。根据 ribC DNA区域内的局部差异设计的引物寡核苷酸已成功用于开发针对 B的物种特异性PCR分析。 henselae B。 clarridgeiae B。金塔纳(Quintana) B。芽孢杆菌。获得的结果表明,核黄素合成基因是这些新兴病原体的PCR定向分化的极佳靶标。所开发的PCR检测方法应增加我们的诊断潜力,以区分 Bartonella 种,尤其是 B。 henselae 和新识别的物种 B。克拉里奇菌。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号