Rossi Franca, Dellaglio Franco, Torriani Sandra
Dipartimento Scientifico e Tecnologico, Università degli Studi di Verona, Strada Le Grazie 15, 37134, Verona, Italy.
Syst Appl Microbiol. 2006 Sep;29(6):463-9. doi: 10.1016/j.syapm.2006.01.001. Epub 2006 Feb 3.
The aim of this study was to investigate the validity of recA gene as a molecular marker for the reliable discrimination and classification of dairy propionibacteria and the closely related species. Regions of the recA gene, varying in size between 613 and 677 nucleotides, were sequenced for Propionibacterium acidipropionici, P. cyclohexanicum, P. freudenreichii, P. jensenii, P. microaerophilum and P. thoenii using degenerate consensus primers constructed by aligning recA sequences of some actinobacteria. The 16S rRNA encoding genes for the type and reference strains of the species P. acidipropionici, P. jensenii and P. thoenii were also sequenced to remove ambiguous positions present in the current database reports, such to improve the classification scheme of reference. As found for other bacterial species, recA sequences permitted a better distinction among the dairy propionibacteria considered than 16S rRNA gene. However, the topology of phylogenetic trees constructed on the recA gene regions sequenced and their putative translations appeared rather different and less statistically valid than the 16S rRNA gene tree. In addition, the possibility of designing PCR-based identification and detection tests on the new recA sequences was demonstrated by assessing specific amplification protocols for P. cyclohexanicum and P. microaerophilum.
本研究的目的是调查recA基因作为分子标记物对乳制品丙酸杆菌及密切相关菌种进行可靠鉴别和分类的有效性。使用通过比对一些放线菌的recA序列构建的简并共有引物,对产酸丙酸杆菌、环己烷丙酸杆菌、费氏丙酸杆菌、詹氏丙酸杆菌、微需氧丙酸杆菌和索氏丙酸杆菌的recA基因区域(大小在613至677个核苷酸之间)进行测序。还对产酸丙酸杆菌、詹氏丙酸杆菌和索氏丙酸杆菌的模式菌株及参考菌株的16S rRNA编码基因进行了测序,以消除当前数据库报告中存在的模糊位置,从而改进参考分类方案。正如在其他细菌物种中所发现的那样,与16S rRNA基因相比,recA序列能更好地区分所研究的乳制品丙酸杆菌。然而,基于测序的recA基因区域及其推定翻译构建的系统发育树的拓扑结构,与16S rRNA基因树相比,显得相当不同且统计学有效性较低。此外,通过评估环己烷丙酸杆菌和微需氧丙酸杆菌的特异性扩增方案,证明了基于新的recA序列设计基于PCR的鉴定和检测试验的可能性。