The diversity of DNA sequences can be analyzed by comparing randomly a
mplified polymorphic DNA, or restriction fragment length polymorphism
fragments of DNA. Such analyses are dependent on the selection of appr
opriate restriction enzyme(s) and/or primers. We have investigated a s
impler approach to providing sensitive and specific genotyping. Cyclic
extension of target sequences with dideoxythymidine generates PCR pro
ducts with variable lengths. We analyzed these variable PCR products b
y scoring the number of variable bands and comparing the scores (numer
ical profiles) to establish similarities. We found that the polymorphi
c lengths of the PCR products were comparable among serologically defi
ned strains. It suggests that this single PCR reaction followed by a o
ne-step electrophoresis yields easily analyzable data that can be comp
ared with data from other gels.