Using Bio-inline reactor to evaluate sanitizer efficacy in removing dual-species biofilms formed by Escherichia coli O157:H7 and Listeria monocytogenes
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Date
2024-06-13
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Citation of Original Publication
Prabhukhot, Grishma S., Charles D. Eggleton, Bryan Vinyard, and Jitendra Patel. “Using Bio-Inline Reactor to Evaluate Sanitizer Efficacy in Removing Dual-Species Biofilms Formed by Escherichia Coli O157:H7 and Listeria Monocytogenes.” Journal of Food Protection 87, no. 8 (August 1, 2024): 100314. https://doi.org/10.1016/j.jfp.2024.100314.
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This work was written as part of one of the author's official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law.
Abstract
The efficacy of a sanitizer in biofilm removal may be influenced by a combination of factors such as sanitizer exposure time and concentration, bacterial species, surface topography and shear stresses. We employed an inline biofilm reactor to investigate the interactions of these variables on biofilm removal with chlorine. The CDC bioreactor was used to grow E. coli O157:H7 and L. monocytogenes biofilms as a single species or with R. insidiosa as a dual-species biofilm on stainless steel, PTFE, and EPDM coupons at shear stresses 0.368 and 2.462 N/m² for 48-hours. Coupons were retrieved from a CDC bioreactor and placed in an inline biofilm reactor and 100, 200 or 500 ppm of chlorine was supplied for 1-and-4 min. Bacterial populations in the biofilms were quantified pre- and post-treatment by plating on selective media. After chlorine treatment, reduction (Log CFU/cm²) in pathogen populations obtained from three replicates were analyzed for statistical significance. A 1-min chlorine treatment (500 ppm), on dual-species E. coli O157:H7 biofilms grown at high shear stress of 2.462 N/m² resulted in significant E. coli O157:H7 reductions on SS 316L (2.79 log CFU/cm²) and PTFE (1.76 log CFU/cm²). Similar trend was also observed for biofilm removal after a 4-min chlorine treatment. Single species E. coli O157:H7 biofilms exhibited higher resistance to chlorine when biofilms were developed at high shear stress. The effect of chlorine in L. monocytogenes removal from dual-species biofilms was dependent primarily on the shear stress at which they were formed rather than the surface topography of materials. Besides surface topography, shear stresses at which biofilms were formed also influenced the effect of sanitizer. The removal of E. coli O157:H7 biofilms from EPDM material may require critical interventions due to difficulty in removing this pathogen. The inline biofilm reactor is novel tool to evaluate the efficacy of a sanitizer in bacterial biofilm removal.