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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 |
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container_title | Journal of applied microbiology |
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creator | Gião, M.S. Blanc, S. Porta, S. 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. |
doi_str_mv | 10.1111/jam.12837 |
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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.</description><identifier>ISSN: 1364-5072</identifier><identifier>EISSN: 1365-2672</identifier><identifier>DOI: 10.1111/jam.12837</identifier><identifier>PMID: 25943582</identifier><identifier>CODEN: JAMIFK</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>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</subject><ispartof>Journal of applied microbiology, 2015-07, Vol.119 (1), p.253-262</ispartof><rights>2015 The Society for Applied Microbiology</rights><rights>2015 The Society for Applied Microbiology.</rights><rights>Copyright © 2015 The Society for Applied Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4917-badff72390635921f2947290832943b28f3f55553427799f676c4915d8ddcd623</citedby><cites>FETCH-LOGICAL-c4917-badff72390635921f2947290832943b28f3f55553427799f676c4915d8ddcd623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25943582$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gião, M.S.</creatorcontrib><creatorcontrib>Blanc, S.</creatorcontrib><creatorcontrib>Porta, S.</creatorcontrib><creatorcontrib>Belenguer, J.</creatorcontrib><creatorcontrib>Keevil, C.W.</creatorcontrib><title>Improved recovery of Listeria monocytogenes from stainless steel and polytetrafluoroethylene surfaces using air/water ablation</title><title>Journal of applied microbiology</title><addtitle>J Appl Microbiol</addtitle><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.</description><subject>air/water ablation</subject><subject>Bacteriological Techniques - methods</subject><subject>Biofilms</subject><subject>biofilms recovery</subject><subject>Food contamination & poisoning</subject><subject>Food Contamination - analysis</subject><subject>Food safety</subject><subject>Food-Processing Industry - instrumentation</subject><subject>Listeria</subject><subject>Listeria monocytogenes</subject><subject>Listeria monocytogenes - growth & development</subject><subject>Listeria monocytogenes - isolation & purification</subject><subject>Listeria monocytogenes - physiology</subject><subject>Microbiology</subject><subject>Polytetrafluoroethylene - analysis</subject><subject>polytetrafluoroethylene surfaces</subject><subject>Stainless steel</subject><subject>Stainless Steel - analysis</subject><subject>stainless steel surfaces</subject><issn>1364-5072</issn><issn>1365-2672</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkUtvFDEQhC0EIiFw4A8gS1zgMFk_xq9jFPEIWsQFziPvTDt45Rkv9kyiufDb6WQDByREX7oOX5W6VYS85Oyc42z2fjznwkrziJxyqVUjtBGP73XbKGbECXlW654xLpnST8mJUK6VyopT8vNqPJR8AwMt0OMuK82BbmOdoURPxzzlfp3zNUxQaSh5pHX2cUpQKyqARP000ENO6wxz8SEtuWSYv68JHbQuJfgenUuN0zX1sWxuPSZTv0t-jnl6Tp4Enyq8eNhn5Nv7d18vPzbbLx-uLi-2Td86bpqdH0IwQjqmpXKCB-FaIxyzEoXcCRtkUDiyFcY4F7TRd0Y12GHoBy3kGXlzzMVnfyxQ526MtYeU_AR5qR031jjLBVP_RzVeoXjbakRf_4Xu81ImfAQp66zTrWJIvT1Sfcm1FgjdocTRl7XjrLvrr8P-uvv-kH31kLjsRhj-kL8LQ2BzBG5jgvXfSd2ni8_HyF91p6Uu</recordid><startdate>201507</startdate><enddate>201507</enddate><creator>Gião, M.S.</creator><creator>Blanc, S.</creator><creator>Porta, S.</creator><creator>Belenguer, J.</creator><creator>Keevil, C.W.</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TM</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7ST</scope><scope>SOI</scope></search><sort><creationdate>201507</creationdate><title>Improved recovery of Listeria monocytogenes from stainless steel and polytetrafluoroethylene surfaces using air/water ablation</title><author>Gião, M.S. ; Blanc, S. ; Porta, S. ; Belenguer, J. ; Keevil, C.W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4917-badff72390635921f2947290832943b28f3f55553427799f676c4915d8ddcd623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>air/water ablation</topic><topic>Bacteriological Techniques - methods</topic><topic>Biofilms</topic><topic>biofilms recovery</topic><topic>Food contamination & poisoning</topic><topic>Food Contamination - analysis</topic><topic>Food safety</topic><topic>Food-Processing Industry - instrumentation</topic><topic>Listeria</topic><topic>Listeria monocytogenes</topic><topic>Listeria monocytogenes - growth & development</topic><topic>Listeria monocytogenes - isolation & purification</topic><topic>Listeria monocytogenes - physiology</topic><topic>Microbiology</topic><topic>Polytetrafluoroethylene - analysis</topic><topic>polytetrafluoroethylene surfaces</topic><topic>Stainless steel</topic><topic>Stainless Steel - analysis</topic><topic>stainless steel surfaces</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gião, M.S.</creatorcontrib><creatorcontrib>Blanc, S.</creatorcontrib><creatorcontrib>Porta, S.</creatorcontrib><creatorcontrib>Belenguer, J.</creatorcontrib><creatorcontrib>Keevil, C.W.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Environment Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Journal of applied microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gião, M.S.</au><au>Blanc, S.</au><au>Porta, S.</au><au>Belenguer, J.</au><au>Keevil, C.W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improved recovery of Listeria monocytogenes from stainless steel and polytetrafluoroethylene surfaces using air/water ablation</atitle><jtitle>Journal of applied microbiology</jtitle><addtitle>J Appl Microbiol</addtitle><date>2015-07</date><risdate>2015</risdate><volume>119</volume><issue>1</issue><spage>253</spage><epage>262</epage><pages>253-262</pages><issn>1364-5072</issn><eissn>1365-2672</eissn><coden>JAMIFK</coden><abstract>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.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>25943582</pmid><doi>10.1111/jam.12837</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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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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