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Improved recovery of Listeria monocytogenes from stainless steel and polytetrafluoroethylene surfaces using air/water ablation

Aims To develop a gentle ablation technique to recover Listeria monocytogenes biofilms from stainless steel (SS) and polytetrafluoroethylene (PTFE) surfaces by using compressed air and water injection. Methods and Results Biofilms were grown for 4, 24 and 48 h or 7 days and a compressed air and wate...

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Published in:Journal of applied microbiology 2015-07, Vol.119 (1), p.253-262
Main Authors: Gião, M.S., Blanc, S., Porta, S., Belenguer, J., Keevil, C.W.
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Language:English
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creator Gião, M.S.
Blanc, S.
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Belenguer, J.
Keevil, C.W.
description Aims To develop a gentle ablation technique to recover Listeria monocytogenes biofilms from stainless steel (SS) and polytetrafluoroethylene (PTFE) surfaces by using compressed air and water injection. Methods and Results Biofilms were grown for 4, 24 and 48 h or 7 days and a compressed air and water flow at 2, 3 and 4 bars was applied for cell removal. Collected cells were quantified for total/dead by staining with SYTO 9/PI double staining and cultivable populations were determined by plating onto brain heart infusion (BHI) agar, while coupon surfaces also were stained with DAPI to quantify in situ the remaining cells. The recovery efficiency was compared to that of conventional swabbing. Results showed that the air/water ablation is able to collect up to 98·6% of cells from SS surfaces while swabbing only recovered 11·2% of biofilm. Moreover, air/water ablation recovered 99·9% of cells from PTFE surfaces. Conclusions The high recovery rate achieved by this technique, along with the fact that cells were able to retain membrane integrity and cultivability, indicate that this device is suitable for the gentle recovery of viable L. monocytogenes biofilm cells. Significance and Impact of the Study This work presents a highly efficient technique to remove, collect and quantify L. monocytogenes from surfaces commonly used in the food industry, which can thus serve as an important aid in verifying cleaning and sanitation as well as in reducing the likelihood of cross‐contamination events.
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Methods and Results Biofilms were grown for 4, 24 and 48 h or 7 days and a compressed air and water flow at 2, 3 and 4 bars was applied for cell removal. Collected cells were quantified for total/dead by staining with SYTO 9/PI double staining and cultivable populations were determined by plating onto brain heart infusion (BHI) agar, while coupon surfaces also were stained with DAPI to quantify in situ the remaining cells. The recovery efficiency was compared to that of conventional swabbing. Results showed that the air/water ablation is able to collect up to 98·6% of cells from SS surfaces while swabbing only recovered 11·2% of biofilm. Moreover, air/water ablation recovered 99·9% of cells from PTFE surfaces. Conclusions The high recovery rate achieved by this technique, along with the fact that cells were able to retain membrane integrity and cultivability, indicate that this device is suitable for the gentle recovery of viable L. monocytogenes biofilm cells. 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subjects air/water ablation
Bacteriological Techniques - methods
Biofilms
biofilms recovery
Food contamination & poisoning
Food Contamination - analysis
Food safety
Food-Processing Industry - instrumentation
Listeria
Listeria monocytogenes
Listeria monocytogenes - growth & development
Listeria monocytogenes - isolation & purification
Listeria monocytogenes - physiology
Microbiology
Polytetrafluoroethylene - analysis
polytetrafluoroethylene surfaces
Stainless steel
Stainless Steel - analysis
stainless steel surfaces
title Improved recovery of Listeria monocytogenes from stainless steel and polytetrafluoroethylene surfaces using air/water ablation
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