The Probelia(TM) Salmonella sp. PCR amplification and detection kits (Sanof
i Diagnostics Pasteur, Marnes La Coquette, France) were evaluated for the r
apid and specific detection of Salmonella agona artificially inoculated int
o skim milk powder and ricotta cheese. The Probelia(TM) results were compar
ed with those obtained using the Australian Standard Method. Using a pure c
ulture of Salm. agona, the detection limit of Probelia(TM) was between 8 an
d 79 cfu ml(-1), equivalent to 0.2-2 cfu per PCR reaction. Detection of Sal
m. agona inoculated in skim milk powder (at 5-10 cfu g(-1), stored at 5, 15
or 25 degrees C) and ricotta cheese (at 1-2, 10-20 and 100-200 cfu per 25
g) was effected by using non-selective enrichment prior to the PCR determin
ations. For all of the 40 milk powder samples and 12 ricotta cheese samples
, the Probelia(TM) results were consistent with those using the Australian
Standard Method. Using Probelia(TM), Salmonella was detected to genus level
in the dairy products within 24-28 h, whereas the cultural technique requi
red 3-4 d for presumptive positive isolates and further time for confirmati
on.