Affiliation:
1. Department of Animal Sciences and Department of Food Science and Human Nutrition, Colorado State University, Fort Collins, Colorado 80523
Abstract
Separate inocula of four strains of Listeria monocytogenes were prepared at 4°C and inoculated (3.58 to 4.67 log10 colony forming units [CFU]/g) in top round ground beef (< 4.0% fat) patties (78.8 ± 6.7 g) of normal (5.47 ± 0.03) or high (6.14 ± 0.08) pH, which were stored (4°C) vacuum-packaged for 56 days and analyzed for L. monocytogenes, total aerobic plate counts (APC) and pH. In normal-pH ground beef, strain N-7143 (serotype 3a), multiplied from 4.25 ± 0.71 log10 CFU/g at day of inoculation to 6.53 ± 0.34 log10 CFU/g at 35 days of storage (P < 0.05); a 2.3 log10 CFU/g increase. Populations of strain Na-19 (serotype 3b) increased 1.8 log10 CFU/g in 35 days of storage, while numbers of strain Na-16 (serotype 1/2a) did not change (P > 0.05) during the 56 days of storage. Strain Scott A (serotype 4b) decreased in numbers from 4.00 ± 1.21 log10 CFU/g at day-0 to 2.72 ± 0.98 log10 CFU/g at 56 days. Populations of strain Scott A were lower (P < 0.05) than other strains after 21 days of storage. In high-pH ground beef, populations of strains Na-19, N-7143 and Na-16 increased (P < 0.05) by 2.87, 2.64 and 2.24 log10 CFU/g, respectively, in 28 days. Populations of strain Scott A did not change significantly (P > 0.05), and they were lower (P< 0.05) than populations of other strains at 28 days. The results indicated that although growth of L. monocytogenes in vacuum-packaged, refrigerated ground beef was slow, it proceeded more rapidly in product of pH values above 6.0, and depended on strain of the pathogen tested.
Publisher
International Association for Food Protection
Subject
Microbiology,Food Science
Cited by
16 articles.
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