Bereswill S, Hinkelmann S, Kist M, Sander A
Department of Microbiology and Hygiene, Institute of Medical Microbiology and Hygiene, University of Freiburg, D-79104 Freiburg, Germany.
J Clin Microbiol. 1999 Oct;37(10):3159-66. doi: 10.1128/JCM.37.10.3159-3166.1999.
The biosynthesis pathway for riboflavin (vitamin B(2)), 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.
核黄素(维生素B2)是必需辅因子黄素单核苷酸和黄素腺嘌呤二核苷酸的前体,其生物合成途径存在于细菌和植物中,但在脊椎动物中不存在。由于它们在细菌物种中保守而在人类中不存在,核黄素合成基因应该非常适合用于检测人类标本中的细菌DNA或通过分子技术区分病原菌。通过互补大肠杆菌中的ribC突变,从人类病原体汉赛巴尔通体基于质粒的DNA文库中分离出一个携带ribD、ribC和ribE基因的DNA片段,这些基因分别编码核黄素脱氨酶(RibD)的同源物和核黄素合成酶的亚基(RibC和RibE)。对先前显示在遗传上不同的汉赛巴尔通体菌株的ribC基因区域进行序列分析,结果表明ribC基因在物种水平上高度保守。使用源自汉赛巴尔通体ribC基因座的引物进行PCR扩增,以分离杆状巴尔通体、克拉氏巴尔通体和五日热巴尔通体中的相应DNA区域。序列分析表明,核黄素合成基因在所有四种巴尔通体物种中都是保守的,并且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成功用于开发物种特异性PCR检测方法,以区分汉赛巴尔通体、克拉氏巴尔通体、五日热巴尔通体和杆状巴尔通体。所得结果表明,核黄素合成基因是这些新出现病原体PCR定向分化的极佳靶标。所开发的PCR检测方法应能提高我们区分巴尔通体物种的诊断潜力,特别是汉赛巴尔通体和新确认的克拉氏巴尔通体。