C. Soumet et al., EVALUATION OF DIFFERENT DNA EXTRACTION PROCEDURES FOR THE DETECTION OF SALMONELLA FROM CHICKEN PRODUCTS BY POLYMERASE CHAIN-REACTION, Letters in applied microbiology, 19(5), 1994, pp. 294-298
Polymerase chain reaction (PCR) was used after a short pre-enrichment
culture to detect Salmonella subspecies in chicken fillets. A direct P
CR assay performed with chicken meat inoculated with Salmonella Typhim
urium produced no PCR products. Six different DNA extraction protocols
were tested to recover efficiently Salmonella DNA after a short incub
ation period. Three of them gave results that were reliable, rapid and
sensitive. Successful protocols used Proteinase K and/or a centrifuga
tion step to concentrate the samples. For reliable detection of Salmon
ella subspecies, a few thousand bacterial cells per mi must be present
. To obtain this number of bacterial cells with an inoculation of abou
t one cell in 25 g of ionized food products, it was necessary to incub
ate samples for at least 10 h before PCR. A larger inoculum of approxi
mately 10 cells in 25 g of ionized food products, required 8 h in cult
ure broth to give positive results by PCR-based assay.