Specific detection and differentiation of two subspecies of Fusobacterium necrophorum by PCR

Abstract The phylogenic relationships of two subspecies of Fusobacterium necrophorum were investigated by randomly amplified polymorphism DNA–polymerase chain reaction (RAPD–PCR). With each of the 12 random primers, the DNA fingerprints generated were subjected to cluster analysis for dendrograms. The analysis indicated that twelve strains were organized into two major clusters, and that all strains of each subspecies were confined to one cluster. Furthermore, two of the random primers examined each generated a unique band in F. n. necrophorum strains. We cloned these specific bands and determined the nucleotide sequences. A search for amino acid sequence homologies revealed that the two specific fragments had significant homology to the rpo B gene of Lactococcus lactis subsp. lactis and the hemagglutinin-related protein gene of Ralstonia solanacearum , respectively. New specific primers designed for the rpo B gene were able to amplify 900 bp fragments from both subspecies. However, the specific primers designed for the hemagglutinin-related protein gene amplified only a 250 bp fragment of the genome of the F. n. necrophorum strains, suggesting that this gene is unique to F. n. necrophorum . These results were further confirmed by dot blot hybridization. Finally, a one-step duplex PCR technique in a single tube for the rapid detection and differentiation of the F. necrophorum subspecies was developed.