Random amplification of polymorphic DNA (RAPD) is proving to be a usef
ul technique in stud!ling the epidemiology of microorganisms. The tech
nique can be troublesome and time consuming to establish due to the es
sentially empirical approach to optimization. By standardization of ce
rtain parameters and use of a commercially available PCR buffer optimi
zation kit, a particularly promising primer was identified and RAPD co
nditions for a highly discriminatory and reproducible characterization
of Salmonella isolates was achieved. In addition, a technique to obta
in reproducible RAPD fingerprints of Salmonella isolates without the n
eed to purify genomic DNA is described.