“…The identification of L. monocytogenes isolates was confirmed by PCR reaction. Two pairs of primers L1 (5′-CAG CAG CCG CGG TAA TAC-3′), L2 (5′-CTC CAT AAA GGT GAC CCT-3′), LM1 (5′-CCT AAG ACG CCA ATC GAA-3′) and LM2 (5′-AAG CAC TTG CAA CTG CTC-3′; Oligo.pl) were applied [ 22 ]. The PCR reaction mixture (25 μL) included 1× PCR buffer (Promega, Madison, WI, USA), 2 mM MgCl 2 (ABO, Gdańsk, Poland), 1.25 mmol dNTPs (Promega, Madison, WI, USA), 0.5 μM of each primer (Oligo.pl), 1 unit of Taq DNA polymerase (Promega, Madison, WI, USA), ultrapure water and DNA isolated from L. monocytogenes .…”