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Comparison of Selective Direct Plating Media for Enumeration and Recovery of L. monocytogenes from Cold-process
Rohinee N Paranjpye1, Gretchen A Pelroy1, Mark E Peterson1
1National Marine Fisheries Service, Northwest Fisheries Science Center, U.S. Department of Commerce, NOAA, Utilization Research Division, 2725 Montlake Boulevard East, Seattle, Washington 98112.
Abstract:
Three selective media were evaluated for direct plating recovery and enumeration of Listeria monocytogenes in the presence of high levels of a variety of microorganisms occurring on cold-process (smoked) salmon products. Sliced salmon was brined to contain either no added salt, 3, or 5% water-phase NaCl, or 3 or 5% NaCl plus 140 ppm NaNO2. The slices were packaged in oxygen-permeable film or sealed under vacuum in oxygen-impermeable film, and stored at 10°C or 5°C until total microbial loads reached 106 to 109 CFU/g. Oxford formulation of Listeria selective agar and Lee's modification of Listeria selective agar achieved quantitative recovery of 102 cells per ml of L. monocytogenes strain Scott A in the presence of diluted slurries of these fish containing 104 to 108 CFU/ml of background organisms. A modification of lithium chloride-phenylethanol-moxalactam agar containing an iron-esculin indicator system sometimes failed because of interfering growth by the background microflora.
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