首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Molecular Analysis of Riboflavin Synthesis Genes in Bartonella henselae and Use of the ribC Gene for Differentiation of Bartonella Species by PCR
【2h】

Molecular Analysis of Riboflavin Synthesis Genes in Bartonella henselae and Use of the ribC Gene 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

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

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 a ribC 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 the ribC 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 four Bartonella 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 Bartonella species, especially B. henselae and the newly recognized species B. clarridgeiae.
机译:核黄素(维生素B2)(必需辅因子黄素单核苷酸和黄素腺嘌呤二核苷酸的前体)的生物合成途径存在于细菌和植物中,而在脊椎动物中则不存在。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。从人类病原体汉塞巴尔通体的基于质粒的DNA文库中分离出一个带有ribD,ribC和ribE基因的DNA片段,分别编码核黄素脱氨酶(RibD)和核黄素合成酶亚基(RibC和RibE)的同源物。通过互补大肠杆菌中的ribC突变。以前显示出遗传差异的亨氏梭菌菌株ribC基因区域的序列分析表明,ribC基因在物种水平上高度保守。用来源于亨氏芽孢杆菌ribC基因座的引物进行PCR扩增,以分离出芽孢杆菌,克拉氏芽孢杆菌和昆塔纳菌中的相应DNA区域。序列分析表明核黄素合成基因是保守的,并且在所有四个巴尔通体物种中显示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检测方法。 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分析方法应增加我们的诊断潜力,以区分 Bartonella 物种,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
代理获取

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