Jersek B, Tcherneva E, Rijpens N, Herman L
Department of Food Science and Technology, University of Ljubijana, Biotechnical Faculty, Slovenia.
Lett Appl Microbiol. 1996 Jul;23(1):55-60. doi: 10.1111/j.1472-765x.1996.tb00028.x.
Repetitive element sequence-based PCR (rep-PCR) was used to generate DNA fingerprints for Listeria spp. Two primer sets (REP 1R-I REP 2-I and ERIC 1R ERIC 2) used in respectively REP- and ERIC-PCR revealed that bacteria of the genus Listeria possess short repetitive extragenic palindromic elements and enterobacterial repetitive intergenic consensus sequences. Specific band profiles obtained by ERIC-PCR enabled the identification of Listeria species. With both REP- and ERIC-PCR the L. monocytogenes serotypes 1/2a, 1/2b, 1/2c, 3b and 4b could be clearly distinguished from each other. Within the serotype 1/2a, REP-PCR showed a higher discriminative potential than ERIC-PCR and a comparable discriminative potential as RAPD combining 3-4 primers.
基于重复元件序列的聚合酶链反应(rep-PCR)被用于生成李斯特菌属的DNA指纹图谱。分别用于REP-PCR和ERIC-PCR的两组引物(REP 1R-I REP 2-I和ERIC 1R ERIC 2)显示,李斯特菌属细菌拥有短的重复基因外回文元件和肠杆菌重复基因间共有序列。通过ERIC-PCR获得的特定条带图谱能够鉴定李斯特菌的种类。使用REP-PCR和ERIC-PCR都能将单核细胞增生李斯特菌血清型1/2a、1/2b、1/2c、3b和4b彼此清晰区分。在血清型1/2a内,REP-PCR显示出比ERIC-PCR更高的鉴别潜力,与组合3-4种引物的随机扩增多态性DNA(RAPD)具有相当的鉴别潜力。