Integrated gold superparticles into lateral flow immunoassays for the rapid and sensitive detection of Escherichia coli O157:H7 in milk
Escherichia coli O157:H7 is a common harmful foodborne pathogen that can cause severe diseases at low infectious doses. Traditional lateral flow immunoassay (LFIA) for the rapid screening of E. coli O157:H7 in food suffers from low sensitivity due to its dependence on 20- to 40-nm gold nanoparticles...
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Veröffentlicht in: | Journal of dairy science 2020-08, Vol.103 (8), p.6940-6949 |
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creator | Li, Yu Chen, Xirui Yuan, Jing Leng, Yuankui Lai, Weihua Huang, Xiaolin Xiong, Yonghua |
description | Escherichia coli O157:H7 is a common harmful foodborne pathogen that can cause severe diseases at low infectious doses. Traditional lateral flow immunoassay (LFIA) for the rapid screening of E. coli O157:H7 in food suffers from low sensitivity due to its dependence on 20- to 40-nm gold nanoparticles (AuNP) with insufficient brightness as labels. To address this issue, we reported for the first time the successful synthesis of gold superparticles (GSP) by encapsulating numerous small AuNP into a polymer nanobead using an evaporation-induced self-assembly method. Results indicated that the resultant GSP exhibited remarkably enhanced absorbance compared with the most widely used 40 nm AuNP in LFIA. In addition, the absorbance of GSP could be easily tuned by varying GSP sizes. Under optimized conditions, we achieved a rapid and sensitive determination of E. coli O157:H7 in milk with a detection limit of 5.95 × 102 cfu/mL when using the GSP with a size of 342 nm as LFIA signal reporters, exhibiting improvement of approximately 32-fold relative to the conventional 40 nm AuNP-LFIA method. We further demonstrated the selectivity, accuracy, reliability, and practicality of the proposed GSP-LFIA strip. In summary, this work offers a new strategy for improving LFIA sensitivity using assembled GSP as markers and demonstrates huge potential in rapidly and sensitively detecting foodborne pathogens. |
doi_str_mv | 10.3168/jds.2019-17934 |
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Traditional lateral flow immunoassay (LFIA) for the rapid screening of E. coli O157:H7 in food suffers from low sensitivity due to its dependence on 20- to 40-nm gold nanoparticles (AuNP) with insufficient brightness as labels. To address this issue, we reported for the first time the successful synthesis of gold superparticles (GSP) by encapsulating numerous small AuNP into a polymer nanobead using an evaporation-induced self-assembly method. Results indicated that the resultant GSP exhibited remarkably enhanced absorbance compared with the most widely used 40 nm AuNP in LFIA. In addition, the absorbance of GSP could be easily tuned by varying GSP sizes. Under optimized conditions, we achieved a rapid and sensitive determination of E. coli O157:H7 in milk with a detection limit of 5.95 × 102 cfu/mL when using the GSP with a size of 342 nm as LFIA signal reporters, exhibiting improvement of approximately 32-fold relative to the conventional 40 nm AuNP-LFIA method. We further demonstrated the selectivity, accuracy, reliability, and practicality of the proposed GSP-LFIA strip. In summary, this work offers a new strategy for improving LFIA sensitivity using assembled GSP as markers and demonstrates huge potential in rapidly and sensitively detecting foodborne pathogens.</description><identifier>ISSN: 0022-0302</identifier><identifier>EISSN: 1525-3198</identifier><identifier>DOI: 10.3168/jds.2019-17934</identifier><identifier>PMID: 32475677</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Escherichia coli O157 - isolation & purification ; Escherichia coli O157:H7 ; Food Microbiology ; Gold ; gold superparticles ; Immunoassay - methods ; Immunoassay - veterinary ; lateral flow immunoassays ; Metal Nanoparticles - chemistry ; milk ; Milk - microbiology ; Reproducibility of Results ; Sensitivity and Specificity</subject><ispartof>Journal of dairy science, 2020-08, Vol.103 (8), p.6940-6949</ispartof><rights>2020 American Dairy Science Association</rights><rights>Copyright © 2020 American Dairy Science Association. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-399b6a9322c749fde20f27bd78c5b7b7fd011bbdd2b1b710a16d7ff872d22d163</citedby><cites>FETCH-LOGICAL-c384t-399b6a9322c749fde20f27bd78c5b7b7fd011bbdd2b1b710a16d7ff872d22d163</cites><orcidid>0000-0001-5141-0841 ; 0000-0002-8908-0443</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.3168/jds.2019-17934$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32475677$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Yu</creatorcontrib><creatorcontrib>Chen, Xirui</creatorcontrib><creatorcontrib>Yuan, Jing</creatorcontrib><creatorcontrib>Leng, Yuankui</creatorcontrib><creatorcontrib>Lai, Weihua</creatorcontrib><creatorcontrib>Huang, Xiaolin</creatorcontrib><creatorcontrib>Xiong, Yonghua</creatorcontrib><title>Integrated gold superparticles into lateral flow immunoassays for the rapid and sensitive detection of Escherichia coli O157:H7 in milk</title><title>Journal of dairy science</title><addtitle>J Dairy Sci</addtitle><description>Escherichia coli O157:H7 is a common harmful foodborne pathogen that can cause severe diseases at low infectious doses. Traditional lateral flow immunoassay (LFIA) for the rapid screening of E. coli O157:H7 in food suffers from low sensitivity due to its dependence on 20- to 40-nm gold nanoparticles (AuNP) with insufficient brightness as labels. To address this issue, we reported for the first time the successful synthesis of gold superparticles (GSP) by encapsulating numerous small AuNP into a polymer nanobead using an evaporation-induced self-assembly method. Results indicated that the resultant GSP exhibited remarkably enhanced absorbance compared with the most widely used 40 nm AuNP in LFIA. In addition, the absorbance of GSP could be easily tuned by varying GSP sizes. Under optimized conditions, we achieved a rapid and sensitive determination of E. coli O157:H7 in milk with a detection limit of 5.95 × 102 cfu/mL when using the GSP with a size of 342 nm as LFIA signal reporters, exhibiting improvement of approximately 32-fold relative to the conventional 40 nm AuNP-LFIA method. We further demonstrated the selectivity, accuracy, reliability, and practicality of the proposed GSP-LFIA strip. In summary, this work offers a new strategy for improving LFIA sensitivity using assembled GSP as markers and demonstrates huge potential in rapidly and sensitively detecting foodborne pathogens.</description><subject>Animals</subject><subject>Escherichia coli O157 - isolation & purification</subject><subject>Escherichia coli O157:H7</subject><subject>Food Microbiology</subject><subject>Gold</subject><subject>gold superparticles</subject><subject>Immunoassay - methods</subject><subject>Immunoassay - veterinary</subject><subject>lateral flow immunoassays</subject><subject>Metal Nanoparticles - chemistry</subject><subject>milk</subject><subject>Milk - microbiology</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><issn>0022-0302</issn><issn>1525-3198</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtOwzAQRS0EglLYskT-gRQ_mjhhhxBQpEpsYB35MW5dkjiy3SK-gN_GUGDHajSae-_MHIQuKJlxWtVXGxNnjNCmoKLh8wM0oSUrC06b-hBNCGGsIJywE3Qa4ya3lJHyGJ1wNhdlJcQEfTwOCVZBJjB45TuD43aEMMqQnO4gYjckj7s8DrLDtvNv2PX9dvAyRvkesfUBpzXgIEdnsByyH4boktsBNpBAJ-cH7C2-i3oNwem1k1j7zuEnWorrhcgLcO-61zN0ZGUX4fynTtHL_d3z7aJYPj083t4sC83reSp406hKNpwxLeaNNcCIZUIZUetSCSWsIZQqZQxTVAlKJK2MsLYWzDBmaMWnaLbP1cHHGMC2Y3C9DO8tJe0X0TYTbb-Itt9Es-Fybxi3qgfzJ_9FmAX1XgD57J2D0EbtYNBgXMj_t8a7_7I_AdpWhzE</recordid><startdate>202008</startdate><enddate>202008</enddate><creator>Li, Yu</creator><creator>Chen, Xirui</creator><creator>Yuan, Jing</creator><creator>Leng, Yuankui</creator><creator>Lai, Weihua</creator><creator>Huang, Xiaolin</creator><creator>Xiong, Yonghua</creator><general>Elsevier Inc</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><orcidid>https://orcid.org/0000-0001-5141-0841</orcidid><orcidid>https://orcid.org/0000-0002-8908-0443</orcidid></search><sort><creationdate>202008</creationdate><title>Integrated gold superparticles into lateral flow immunoassays for the rapid and sensitive detection of Escherichia coli O157:H7 in milk</title><author>Li, Yu ; Chen, Xirui ; Yuan, Jing ; Leng, Yuankui ; Lai, Weihua ; Huang, Xiaolin ; Xiong, Yonghua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-399b6a9322c749fde20f27bd78c5b7b7fd011bbdd2b1b710a16d7ff872d22d163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Escherichia coli O157 - isolation & purification</topic><topic>Escherichia coli O157:H7</topic><topic>Food Microbiology</topic><topic>Gold</topic><topic>gold superparticles</topic><topic>Immunoassay - methods</topic><topic>Immunoassay - veterinary</topic><topic>lateral flow immunoassays</topic><topic>Metal Nanoparticles - chemistry</topic><topic>milk</topic><topic>Milk - microbiology</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Yu</creatorcontrib><creatorcontrib>Chen, Xirui</creatorcontrib><creatorcontrib>Yuan, Jing</creatorcontrib><creatorcontrib>Leng, Yuankui</creatorcontrib><creatorcontrib>Lai, Weihua</creatorcontrib><creatorcontrib>Huang, Xiaolin</creatorcontrib><creatorcontrib>Xiong, Yonghua</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of dairy science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Yu</au><au>Chen, Xirui</au><au>Yuan, Jing</au><au>Leng, Yuankui</au><au>Lai, Weihua</au><au>Huang, Xiaolin</au><au>Xiong, Yonghua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Integrated gold superparticles into lateral flow immunoassays for the rapid and sensitive detection of Escherichia coli O157:H7 in milk</atitle><jtitle>Journal of dairy science</jtitle><addtitle>J Dairy Sci</addtitle><date>2020-08</date><risdate>2020</risdate><volume>103</volume><issue>8</issue><spage>6940</spage><epage>6949</epage><pages>6940-6949</pages><issn>0022-0302</issn><eissn>1525-3198</eissn><abstract>Escherichia coli O157:H7 is a common harmful foodborne pathogen that can cause severe diseases at low infectious doses. Traditional lateral flow immunoassay (LFIA) for the rapid screening of E. coli O157:H7 in food suffers from low sensitivity due to its dependence on 20- to 40-nm gold nanoparticles (AuNP) with insufficient brightness as labels. To address this issue, we reported for the first time the successful synthesis of gold superparticles (GSP) by encapsulating numerous small AuNP into a polymer nanobead using an evaporation-induced self-assembly method. Results indicated that the resultant GSP exhibited remarkably enhanced absorbance compared with the most widely used 40 nm AuNP in LFIA. In addition, the absorbance of GSP could be easily tuned by varying GSP sizes. Under optimized conditions, we achieved a rapid and sensitive determination of E. coli O157:H7 in milk with a detection limit of 5.95 × 102 cfu/mL when using the GSP with a size of 342 nm as LFIA signal reporters, exhibiting improvement of approximately 32-fold relative to the conventional 40 nm AuNP-LFIA method. We further demonstrated the selectivity, accuracy, reliability, and practicality of the proposed GSP-LFIA strip. In summary, this work offers a new strategy for improving LFIA sensitivity using assembled GSP as markers and demonstrates huge potential in rapidly and sensitively detecting foodborne pathogens.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32475677</pmid><doi>10.3168/jds.2019-17934</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-5141-0841</orcidid><orcidid>https://orcid.org/0000-0002-8908-0443</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Escherichia coli O157 - isolation & purification Escherichia coli O157:H7 Food Microbiology Gold gold superparticles Immunoassay - methods Immunoassay - veterinary lateral flow immunoassays Metal Nanoparticles - chemistry milk Milk - microbiology Reproducibility of Results Sensitivity and Specificity |
title | Integrated gold superparticles into lateral flow immunoassays for the rapid and sensitive detection of Escherichia coli O157:H7 in milk |
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