Co-migration of RAPD-PCR amplicons from Aeromonas hydrophila

• Published in: FEMS microbiology letters 1998-07, Vol.164 (1), p.35-38
• Main Authors: Oakey, Helen J., Gibson, Lewis F., George, Anthony M.
• Format: Article
• Language: English
• Subjects: Aeromonas hydrophila; Aeromonas hydrophila - classification; Aeromonas hydrophila - genetics; Amplification; Bacteriological methods and techniques used in bacteriology; Bacteriology; Base Sequence; Biological and medical sciences; Blotting, Southern; Co‐migration; Deoxyribonucleic acid; DNA; DNA Fingerprinting; DNA polymerase; DNA, Bacterial - genetics; DNA-directed DNA polymerase; Fingerprints; Fragments; Fundamental and applied biological sciences. Psychology; Gels; Genetic relationship; Genomes; Microbiology; Microorganisms; Molecular Sequence Data; Nucleotides; Polymerase chain reaction; Random amplified polymorphic DNA; Random amplified polymorphic DNA polymerase chain reaction; Random Amplified Polymorphic DNA Technique; Species Specificity
• ISSN: 0378-1097; 1574-6968
• DOI: 10.1111/j.1574-6968.1998.tb13064.x

Abstract Random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) uses arbitrary primers and low stringency annealing conditions to amplify anonymous DNA fragments which are then depicted in agarose gels. RAPD-PCR fingerprints have been used for typing and differentiation of bacteria and, increasingly, for the study of genetic relationships between strains and species of microorganisms, plants and animals. The analysis of such fingerprints is based upon the assumption that co-migration of amplicons does not occur and that any given band contains a single amplicon. This report shows that co-migration of fragments of nearly identical size, but different nucleotide sequences, occurs between different isolates and within single RAPD-PCR bands from Aeromonas hydrophila. The possibility of the same phenomenon occurring for other prokaryotic or eukaryotic genomes argues for caution in the interpretation of RAPD-PCR fingerprints.