Assous M V, Postic D, Paul G, Névot P, Baranton G
Laboratoire de Bactériologie, Faculté de Médecine Cochin-Port Royal, Paris, France.
FEMS Microbiol Lett. 1994 Aug 1;121(1):93-8. doi: 10.1111/j.1574-6968.1994.tb07081.x.
We developed a quick typing method for Borrelia burgdorferi sensu lato strains using a fla gene-based PCR assay, followed by dot blot hybridization with non-radioactive species-specific probes. Thirty-six out of 46 strains belonged to one of the four described species (B. burgdorferi sensu stricto n = 11, B. garinii n = 11, B. afzelii n = 9 and B. japonica n = 5) and hybridized with its own species-specific probe. Among the 10 remaining American strains, two new additional genomic groups were identified. This finding was confirmed by direct sequencing of the fla gene-derived amplicons and whole DNA hybridization.
我们开发了一种针对伯氏疏螺旋体狭义菌株的快速分型方法,该方法采用基于fla基因的聚合酶链反应(PCR)分析,随后用非放射性物种特异性探针进行斑点印迹杂交。46株菌株中有36株属于已描述的四个物种之一(狭义伯氏疏螺旋体n = 11、伽氏疏螺旋体n = 11、阿氏疏螺旋体n = 9和日本疏螺旋体n = 5),并与其自身的物种特异性探针杂交。在其余10株美国菌株中,鉴定出两个新的基因组群。通过对fla基因衍生扩增子的直接测序和全DNA杂交证实了这一发现。