This research was carried out to assess the ability of L. monocytogenes for adhesion and growth in bio lm on stainless steel coupons under different stressing conditions (NaCl, curing salts and quaternary ammonium compounds -QAC), besides determining the expression of different genes involved in bio lm formation and stress response. Results from crystal violet assay revealed that one isolate carrying a premature stop codon (PMSC) in agrC gene formed high-density bio lms in the presence of QAC or cure salts (7.5% and 10%). Reverse Transcriptase-qPCR results revealed that isolates of L. monocytogenes lineages I and II presented differences in transcriptional pro le of genes related to bio lm formation and adaptation to environmental conditions. In conclusion, our results demonstrated how L. monocytogenes can survive, multiply and form bio lm under adverse conditions related to food processing environments. Differences in transcriptional expression were observed, highlighting the role of regulatory gene networks for particular serotypes under different stress responses.