Purpose: This study aimed to genetically characterize L. monocytogenes isolates obtained from bovine carcasses and beef processing facilities and to evaluate their adhesion capabilities.
Methods: DNA from twenty-nine L. monocytogenes isolates was subjected to enzymatic restriction digestion using AscI and ApaI. All isolates were evaluated for the adhesion capability in microtitre plates considering the following variables: inoculum concentration, culture media, carbohydrate source, NaCl concentration, incubation temperature, and pH. Results were compared by ANOVA and Tukey (P < 0.05).
Results: Two clusters were identified for serotypes 4b and 1/2a, with similarities of 48% and 68%, respectively. The isolates presented best adhesion performance when tested at 8 log CFU/ml, being classified according to its capability as weak (8 isolates), moderate (17) or strong (4). The isolates showed higher adhesion capability in non-diluted culture media, medium at pH 7.0, incubation at 25 °C and 37 °C, and medium with NaCl concentrations of 5% and 7%. No relevant differences were observed for adhesion capability with respect to the carbohydrate source (P > 0.05).
Significance: The results indicated that despite a wide variation of characterized PFGE profiles, L. monocytognes adhesion might be related to optimal growing conditions.