Efficient Separation and Sensitive Detection of Listeria monocytogenes Using an Impedance Immunosensor Based on Magnetic Nanoparticles, a Microfluidic Chip, and an Interdigitated Microelectrode
Listeria monocytogenes continues to be a major foodborne pathogen that causes food poisoning, and sometimes death, among immunosuppressed people and abortion among pregnant women. In this study, magnetic nanoparticles with a diameter of 30 nm were functionalized with anti-L. monocytogenes antibodies...
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Veröffentlicht in: | Journal of food protection 2012-11, Vol.75 (11), p.1951-1959 |
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creator | KANAYEVA, Damira A RONGHUI W RHOADS, Douglas ERF, Gisela F SLAVIK, Michael F TUNG, Steve YANBIN LI |
description | Listeria monocytogenes continues to be a major foodborne pathogen that causes food poisoning, and sometimes death, among immunosuppressed people and abortion among pregnant women. In this study, magnetic nanoparticles with a diameter of 30 nm were functionalized with anti-L. monocytogenes antibodies via biotin-streptavidin bonds to become immunomagnetic nanoparticles (IMNPs) to capture L. monocytogenes in a sample during a 2-h immunoreaction. A magnetic separator was used to collect and hold the IMNPs-L. monocytogenes complex while the supernatants were removed. After the washing step, the nanoparticle-L. monocytogenes complex was separated from the sample and injected into a microfluidic chip. The impedance change caused by L. monocytogenes was measured by an impedance analyzer through the interdigitated microelectrode in the microfluidic chip. For L. monocytogenes in phosphate-buffered saline solution, up to 75% of the cells in the sample could be separated, and as few as three to five cells in the microfluidic chip could be detected, which is equivalent to 10(3) CFU/ml of cells in the original sample. The detection of L. monocytogenes was not interfered with by other major foodborne bacteria, including E. coli O157:H7, E. coli K-12, L. innocua, Salmonella Typhimurium, and Staphylococcus aureus. A linear correlation (R(2) = 0.86) was found between the impedance change and the number of L. monocytogenes in a range of 10(3) to 10(7) CFU/ml. Equivalent circuit analysis indicated that the impedance change was mainly due to the decrease in medium resistance when the IMNPs-L. monocytogenes complexes existed in mannitol solution. Finally, the immunosensor was evaluated with food sample tests; the results showed that, without preenrichment and labeling, 10(4) and 10(5) CFU/ml L. monocytogenes in lettuce, milk, and ground beef samples could be detected in 3 h. |
doi_str_mv | 10.4315/0362-028X.JFP-11-516 |
format | Article |
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In this study, magnetic nanoparticles with a diameter of 30 nm were functionalized with anti-L. monocytogenes antibodies via biotin-streptavidin bonds to become immunomagnetic nanoparticles (IMNPs) to capture L. monocytogenes in a sample during a 2-h immunoreaction. A magnetic separator was used to collect and hold the IMNPs-L. monocytogenes complex while the supernatants were removed. After the washing step, the nanoparticle-L. monocytogenes complex was separated from the sample and injected into a microfluidic chip. The impedance change caused by L. monocytogenes was measured by an impedance analyzer through the interdigitated microelectrode in the microfluidic chip. For L. monocytogenes in phosphate-buffered saline solution, up to 75% of the cells in the sample could be separated, and as few as three to five cells in the microfluidic chip could be detected, which is equivalent to 10(3) CFU/ml of cells in the original sample. The detection of L. monocytogenes was not interfered with by other major foodborne bacteria, including E. coli O157:H7, E. coli K-12, L. innocua, Salmonella Typhimurium, and Staphylococcus aureus. A linear correlation (R(2) = 0.86) was found between the impedance change and the number of L. monocytogenes in a range of 10(3) to 10(7) CFU/ml. Equivalent circuit analysis indicated that the impedance change was mainly due to the decrease in medium resistance when the IMNPs-L. monocytogenes complexes existed in mannitol solution. Finally, the immunosensor was evaluated with food sample tests; the results showed that, without preenrichment and labeling, 10(4) and 10(5) CFU/ml L. monocytogenes in lettuce, milk, and ground beef samples could be detected in 3 h.</description><identifier>ISSN: 0362-028X</identifier><identifier>EISSN: 1944-9097</identifier><identifier>DOI: 10.4315/0362-028X.JFP-11-516</identifier><identifier>PMID: 23127703</identifier><identifier>CODEN: JFPRDR</identifier><language>eng</language><publisher>Des Moines, IA: International Association for Food Protection</publisher><subject>Antibodies ; Antibodies, Bacterial - analysis ; Bacteria ; Biological and medical sciences ; Biosensors ; Biotin ; Colony Count, Microbial ; Consumer Product Safety ; E coli ; Food contamination ; Food contamination & poisoning ; Food Contamination - analysis ; Food industries ; Food Microbiology ; Food safety ; Fundamental and applied biological sciences. Psychology ; General aspects ; Humans ; Immunomagnetic Separation - methods ; Impedance ; Listeria ; Listeria monocytogenes - immunology ; Listeria monocytogenes - isolation & purification ; Medical research ; Methods of analysis, processing and quality control, regulation, standards ; Molecular biology ; Nanoparticles ; Pathogens ; Salmonella ; Sensitivity and Specificity</subject><ispartof>Journal of food protection, 2012-11, Vol.75 (11), p.1951-1959</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright Allen Press Publishing Services Nov 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-c51e8bff80ca333fe529cbf06fbee7274787e3bdc89c1b01d0eb2ac5c53a1cba3</citedby><cites>FETCH-LOGICAL-c411t-c51e8bff80ca333fe529cbf06fbee7274787e3bdc89c1b01d0eb2ac5c53a1cba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26584660$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23127703$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KANAYEVA, Damira A</creatorcontrib><creatorcontrib>RONGHUI W</creatorcontrib><creatorcontrib>RHOADS, Douglas</creatorcontrib><creatorcontrib>ERF, Gisela F</creatorcontrib><creatorcontrib>SLAVIK, Michael F</creatorcontrib><creatorcontrib>TUNG, Steve</creatorcontrib><creatorcontrib>YANBIN LI</creatorcontrib><title>Efficient Separation and Sensitive Detection of Listeria monocytogenes Using an Impedance Immunosensor Based on Magnetic Nanoparticles, a Microfluidic Chip, and an Interdigitated Microelectrode</title><title>Journal of food protection</title><addtitle>J Food Prot</addtitle><description>Listeria monocytogenes continues to be a major foodborne pathogen that causes food poisoning, and sometimes death, among immunosuppressed people and abortion among pregnant women. In this study, magnetic nanoparticles with a diameter of 30 nm were functionalized with anti-L. monocytogenes antibodies via biotin-streptavidin bonds to become immunomagnetic nanoparticles (IMNPs) to capture L. monocytogenes in a sample during a 2-h immunoreaction. A magnetic separator was used to collect and hold the IMNPs-L. monocytogenes complex while the supernatants were removed. After the washing step, the nanoparticle-L. monocytogenes complex was separated from the sample and injected into a microfluidic chip. The impedance change caused by L. monocytogenes was measured by an impedance analyzer through the interdigitated microelectrode in the microfluidic chip. For L. monocytogenes in phosphate-buffered saline solution, up to 75% of the cells in the sample could be separated, and as few as three to five cells in the microfluidic chip could be detected, which is equivalent to 10(3) CFU/ml of cells in the original sample. The detection of L. monocytogenes was not interfered with by other major foodborne bacteria, including E. coli O157:H7, E. coli K-12, L. innocua, Salmonella Typhimurium, and Staphylococcus aureus. A linear correlation (R(2) = 0.86) was found between the impedance change and the number of L. monocytogenes in a range of 10(3) to 10(7) CFU/ml. Equivalent circuit analysis indicated that the impedance change was mainly due to the decrease in medium resistance when the IMNPs-L. monocytogenes complexes existed in mannitol solution. Finally, the immunosensor was evaluated with food sample tests; the results showed that, without preenrichment and labeling, 10(4) and 10(5) CFU/ml L. monocytogenes in lettuce, milk, and ground beef samples could be detected in 3 h.</description><subject>Antibodies</subject><subject>Antibodies, Bacterial - analysis</subject><subject>Bacteria</subject><subject>Biological and medical sciences</subject><subject>Biosensors</subject><subject>Biotin</subject><subject>Colony Count, Microbial</subject><subject>Consumer Product Safety</subject><subject>E coli</subject><subject>Food contamination</subject><subject>Food contamination & poisoning</subject><subject>Food Contamination - analysis</subject><subject>Food industries</subject><subject>Food Microbiology</subject><subject>Food safety</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects</subject><subject>Humans</subject><subject>Immunomagnetic Separation - methods</subject><subject>Impedance</subject><subject>Listeria</subject><subject>Listeria monocytogenes - immunology</subject><subject>Listeria monocytogenes - isolation & purification</subject><subject>Medical research</subject><subject>Methods of analysis, processing and quality control, regulation, standards</subject><subject>Molecular biology</subject><subject>Nanoparticles</subject><subject>Pathogens</subject><subject>Salmonella</subject><subject>Sensitivity and Specificity</subject><issn>0362-028X</issn><issn>1944-9097</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpFkd1u1DAQhS0EotvCGyBkCXHXFP_E-bmkSwtFW0CCStxFjjNeXCV2sB2kPl7fjNntUq48Hn_nzMiHkFecnZWSq3dMVqJgovl59vnyW8F5oXj1hKx4W5ZFy9r6KVk9IkfkOKVbxphoRfWcHAnJRV0zuSL3F9Y648Bn-h1mHXV2wVPtB7z65LL7A_QDZDD7frB041KG6DSdgg_mLocteEj0Jjm_RR29mmYYtDeA1bT4kNAmRHquEwwULa711kN2hn7RPuBALEdIp1TTa2disOPiBnxd_3Lz6X6PnafHkYPbuqwzuuxBGHGnGAZ4QZ5ZPSZ4eThPyM3lxY_1p2Lz9ePV-v2mMCXnuTCKQ9Nb2zCjpZQWlGhNb1lle4Ba1GXd1CD7wTSt4T3jA4NeaKOMkpqbXssT8ubBd47h9wIpd7dhiR5HdpxzpVohhEKqfKBwxZQi2G6ObtLxruOs2-XW7ULpdqF0mBtKO8wNZa8P5ks_wfAo-hcUAm8PgE5GjzbiF7v0n6tUU1YVk38BWfumKw</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>KANAYEVA, Damira A</creator><creator>RONGHUI W</creator><creator>RHOADS, Douglas</creator><creator>ERF, Gisela F</creator><creator>SLAVIK, Michael F</creator><creator>TUNG, Steve</creator><creator>YANBIN LI</creator><general>International Association for Food Protection</general><general>Elsevier Limited</general><scope>IQODW</scope><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>3V.</scope><scope>7RQ</scope><scope>7WY</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>883</scope><scope>88E</scope><scope>88I</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FL</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FRNLG</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K60</scope><scope>K6~</scope><scope>K9.</scope><scope>L.-</scope><scope>M0F</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PATMY</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>Q9U</scope></search><sort><creationdate>20121101</creationdate><title>Efficient Separation and Sensitive Detection of Listeria monocytogenes Using an Impedance Immunosensor Based on Magnetic Nanoparticles, a Microfluidic Chip, and an Interdigitated Microelectrode</title><author>KANAYEVA, Damira A ; RONGHUI W ; RHOADS, Douglas ; ERF, Gisela F ; SLAVIK, Michael F ; TUNG, Steve ; YANBIN LI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-c51e8bff80ca333fe529cbf06fbee7274787e3bdc89c1b01d0eb2ac5c53a1cba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Antibodies</topic><topic>Antibodies, Bacterial - analysis</topic><topic>Bacteria</topic><topic>Biological and medical sciences</topic><topic>Biosensors</topic><topic>Biotin</topic><topic>Colony Count, Microbial</topic><topic>Consumer Product Safety</topic><topic>E coli</topic><topic>Food contamination</topic><topic>Food contamination & poisoning</topic><topic>Food Contamination - analysis</topic><topic>Food industries</topic><topic>Food Microbiology</topic><topic>Food safety</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects</topic><topic>Humans</topic><topic>Immunomagnetic Separation - methods</topic><topic>Impedance</topic><topic>Listeria</topic><topic>Listeria monocytogenes - immunology</topic><topic>Listeria monocytogenes - isolation & purification</topic><topic>Medical research</topic><topic>Methods of analysis, processing and quality control, regulation, standards</topic><topic>Molecular biology</topic><topic>Nanoparticles</topic><topic>Pathogens</topic><topic>Salmonella</topic><topic>Sensitivity and Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KANAYEVA, Damira A</creatorcontrib><creatorcontrib>RONGHUI W</creatorcontrib><creatorcontrib>RHOADS, Douglas</creatorcontrib><creatorcontrib>ERF, Gisela F</creatorcontrib><creatorcontrib>SLAVIK, Michael F</creatorcontrib><creatorcontrib>TUNG, Steve</creatorcontrib><creatorcontrib>YANBIN LI</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Career & Technical Education Database</collection><collection>ABI/INFORM Collection</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ABI/INFORM Trade & Industry (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ABI/INFORM Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Business Premium Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Business Premium Collection (Alumni)</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Business Collection (Alumni Edition)</collection><collection>ProQuest Business Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ABI/INFORM Professional Advanced</collection><collection>ABI/INFORM Trade & Industry</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Environmental Science Database</collection><collection>ProQuest One Business</collection><collection>ProQuest One Business (Alumni)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of food protection</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KANAYEVA, Damira A</au><au>RONGHUI W</au><au>RHOADS, Douglas</au><au>ERF, Gisela F</au><au>SLAVIK, Michael F</au><au>TUNG, Steve</au><au>YANBIN LI</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient Separation and Sensitive Detection of Listeria monocytogenes Using an Impedance Immunosensor Based on Magnetic Nanoparticles, a Microfluidic Chip, and an Interdigitated Microelectrode</atitle><jtitle>Journal of food protection</jtitle><addtitle>J Food Prot</addtitle><date>2012-11-01</date><risdate>2012</risdate><volume>75</volume><issue>11</issue><spage>1951</spage><epage>1959</epage><pages>1951-1959</pages><issn>0362-028X</issn><eissn>1944-9097</eissn><coden>JFPRDR</coden><abstract>Listeria monocytogenes continues to be a major foodborne pathogen that causes food poisoning, and sometimes death, among immunosuppressed people and abortion among pregnant women. In this study, magnetic nanoparticles with a diameter of 30 nm were functionalized with anti-L. monocytogenes antibodies via biotin-streptavidin bonds to become immunomagnetic nanoparticles (IMNPs) to capture L. monocytogenes in a sample during a 2-h immunoreaction. A magnetic separator was used to collect and hold the IMNPs-L. monocytogenes complex while the supernatants were removed. After the washing step, the nanoparticle-L. monocytogenes complex was separated from the sample and injected into a microfluidic chip. The impedance change caused by L. monocytogenes was measured by an impedance analyzer through the interdigitated microelectrode in the microfluidic chip. For L. monocytogenes in phosphate-buffered saline solution, up to 75% of the cells in the sample could be separated, and as few as three to five cells in the microfluidic chip could be detected, which is equivalent to 10(3) CFU/ml of cells in the original sample. The detection of L. monocytogenes was not interfered with by other major foodborne bacteria, including E. coli O157:H7, E. coli K-12, L. innocua, Salmonella Typhimurium, and Staphylococcus aureus. A linear correlation (R(2) = 0.86) was found between the impedance change and the number of L. monocytogenes in a range of 10(3) to 10(7) CFU/ml. Equivalent circuit analysis indicated that the impedance change was mainly due to the decrease in medium resistance when the IMNPs-L. monocytogenes complexes existed in mannitol solution. Finally, the immunosensor was evaluated with food sample tests; the results showed that, without preenrichment and labeling, 10(4) and 10(5) CFU/ml L. monocytogenes in lettuce, milk, and ground beef samples could be detected in 3 h.</abstract><cop>Des Moines, IA</cop><pub>International Association for Food Protection</pub><pmid>23127703</pmid><doi>10.4315/0362-028X.JFP-11-516</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Antibodies, Bacterial - analysis Bacteria Biological and medical sciences Biosensors Biotin Colony Count, Microbial Consumer Product Safety E coli Food contamination Food contamination & poisoning Food Contamination - analysis Food industries Food Microbiology Food safety Fundamental and applied biological sciences. Psychology General aspects Humans Immunomagnetic Separation - methods Impedance Listeria Listeria monocytogenes - immunology Listeria monocytogenes - isolation & purification Medical research Methods of analysis, processing and quality control, regulation, standards Molecular biology Nanoparticles Pathogens Salmonella Sensitivity and Specificity |
title | Efficient Separation and Sensitive Detection of Listeria monocytogenes Using an Impedance Immunosensor Based on Magnetic Nanoparticles, a Microfluidic Chip, and an Interdigitated Microelectrode |
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