An article (PATHIRAJAH et al. 2022, Influence of Different Stainless Steel Finishes on Biofilm Formation by Listeria monocytogenes, J Food Prot (2022) 85 (11): 1584–1593) investigates the effect of Stainless steel (SS) roughness on the attachment of Listeria monocytogenes. The goal was to see whether there were finishes with significantly lower bacterial attachment. The number of adhered cells increased with time on all stainless steel finishes. Eight-hour results showed a significant difference (P< 0.05) in biofilm cell counts in biofilms between the roughest and finest surfaces. Data gained after 4-h, 24-h, and 24-h plus an additional 24-h continuous flow cultivation showed no significant difference in attachment among surfaces. No correlation between roughness data and attachment was found after all four incubation times, suggesting that roughness values at these ranges are insufficient in determining the surfaces' affinity to bacteria. Overall, this study suggests that roughness values cannot be used to predict the degree of L. monocytogenes attachment to a specific stainless steel surface. @ https://meridian.allenpress.com/jfp/article-abstract/85/11/1584/485622/Influence-of-Different-Stainless-Steel-Finishes-on?redirectedFrom=fulltext
Influence of stainless steel roughness on biofilm formation by Listeria monocytogenes
ABSTRACT. Biofilm formation of Listeria monocytogenes on stainless steel, a widely used abiotic surface in the food processing industry, was investigated by focusing on the attachment tendency and behavior of L. monocytogenes 08-5578 on eight different stainless steel surfaces: glass bead blasted (rough and fine), deburred (Timesaver), drum deburred, pickled, pickled and drum polished, electrolytic polished, and cold rolled (untreated control). The aim was to see whether there are finishes with significantly lower bacterial attachment. Surface roughness data (measured via four roughness parameters), determined by interferometry, was also compared with the number of adhering cells to detect possible correlations. Cultivation of L. monocytogenes biofilms was carried out using a CDC biofilm reactor with 1% tryptic soy broth set at 20°C for 4, 8, and 24 h. In addition, a cultivation trial was run with continuous nutrient flow (1% tryptic soy broth, 6.2 mL/min) for 24 h. Eight-hour results showed a significant difference (P < 0.05) in biofilm cell counts in biofilms between the glass bead–blasted surfaces (3.23 and 3.26 log CFU/cm2 for the fine and rough, respectively) and deburred (Timesaver) surface (2.57 log CFU/cm2), between drum deburred and deburred (Timesaver) surface (3.41 versus 2.57 log CFU/cm2), and between drum deburred and pickled surface (3.41 versus 2.77 log CFU/cm2). Data gained after 4-h, 24-h, and 24-h plus an additional 24-h continuous flow cultivation showed no significant difference in attachment among surfaces. No correlation between roughness data and attachment was found after all four incubation times, suggesting that roughness values, at these ranges, are insufficient in determining the surfaces' affinity to bacteria. Overall, this study suggests that roughness values cannot be used to predict the degree of L. monocytogenes attachment to a specific stainless steel surface.HIGHLIGHTSThe number of adhered cells increased with time on all stainless steel finishes.There were significant differences in adhered cell counts between surfaces after 8 h of cultivation.No correlation between roughness data and attachment was observed.Range of roughness studied cannot be used to predict degree of Listeria attachment.