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A bead-based suspension array for the serological detection of Trichinella in pigs
The feasibility of using bead-based suspension arrays to detect serological evidence of Trichinella in pigs was assessed. Trichinella spiralis excretory–secretory antigen was covalently coupled to paramagnetic beads and used to bind serum antibodies, which were subsequently detected using anti-swine...
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Published in: | The veterinary journal (1997) 2013-06, Vol.196 (3), p.439-444 |
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container_title | The veterinary journal (1997) |
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creator | van der Wal, F.J. Achterberg, R.P. Kant, A. Maassen, C.B.M. |
description | The feasibility of using bead-based suspension arrays to detect serological evidence of Trichinella in pigs was assessed. Trichinella spiralis excretory–secretory antigen was covalently coupled to paramagnetic beads and used to bind serum antibodies, which were subsequently detected using anti-swine antibody. The assay was evaluated by testing pig sera from farms where trichinellosis was endemic and comparing the results with those obtained using two commercially available ELISAs. With cut-offs established by receiver operating characteristic (ROC) analysis, digestion-negative sera from a Trichinella-free population of pigs were deemed seronegative. When anti-swine antibody was replaced with protein A/G, higher test sensitivity (94% vs. 88%) at similar test specificity (95%), was achieved. The potential use of this assay in species other than swine was also demonstrated by testing human sera. |
doi_str_mv | 10.1016/j.tvjl.2012.10.029 |
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Trichinella spiralis excretory–secretory antigen was covalently coupled to paramagnetic beads and used to bind serum antibodies, which were subsequently detected using anti-swine antibody. The assay was evaluated by testing pig sera from farms where trichinellosis was endemic and comparing the results with those obtained using two commercially available ELISAs. With cut-offs established by receiver operating characteristic (ROC) analysis, digestion-negative sera from a Trichinella-free population of pigs were deemed seronegative. When anti-swine antibody was replaced with protein A/G, higher test sensitivity (94% vs. 88%) at similar test specificity (95%), was achieved. The potential use of this assay in species other than swine was also demonstrated by testing human sera.</description><identifier>ISSN: 1090-0233</identifier><identifier>EISSN: 1532-2971</identifier><identifier>DOI: 10.1016/j.tvjl.2012.10.029</identifier><identifier>PMID: 23177539</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; antibodies ; antigens ; blood serum ; enzyme-linked immunosorbent assay ; Enzyme-Linked Immunosorbent Assay - veterinary ; farms ; Human ; humans ; immunoassay ; Indexing in process ; linked-immunosorbent-assay ; multiplexed luminex assay ; nonstructural proteins ; Pig ; Sensitivity and Specificity ; serodiagnosis ; Serologic Tests - veterinary ; Serology ; spiralis ; Suspension array ; Swine ; Swine Diseases - blood ; Swine Diseases - diagnosis ; Swine Diseases - parasitology ; Trichinella - isolation & purification ; Trichinella spiralis ; Trichinellosis - blood ; Trichinellosis - diagnosis ; Trichinellosis - parasitology ; Trichinellosis - veterinary ; trichinosis ; virus ; Zoonosis</subject><ispartof>The veterinary journal (1997), 2013-06, Vol.196 (3), p.439-444</ispartof><rights>2012 Elsevier Ltd</rights><rights>Copyright © 2012 Elsevier Ltd. 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Trichinella spiralis excretory–secretory antigen was covalently coupled to paramagnetic beads and used to bind serum antibodies, which were subsequently detected using anti-swine antibody. The assay was evaluated by testing pig sera from farms where trichinellosis was endemic and comparing the results with those obtained using two commercially available ELISAs. With cut-offs established by receiver operating characteristic (ROC) analysis, digestion-negative sera from a Trichinella-free population of pigs were deemed seronegative. When anti-swine antibody was replaced with protein A/G, higher test sensitivity (94% vs. 88%) at similar test specificity (95%), was achieved. The potential use of this assay in species other than swine was also demonstrated by testing human sera.</description><subject>Animals</subject><subject>antibodies</subject><subject>antigens</subject><subject>blood serum</subject><subject>enzyme-linked immunosorbent assay</subject><subject>Enzyme-Linked Immunosorbent Assay - veterinary</subject><subject>farms</subject><subject>Human</subject><subject>humans</subject><subject>immunoassay</subject><subject>Indexing in process</subject><subject>linked-immunosorbent-assay</subject><subject>multiplexed luminex assay</subject><subject>nonstructural proteins</subject><subject>Pig</subject><subject>Sensitivity and Specificity</subject><subject>serodiagnosis</subject><subject>Serologic Tests - veterinary</subject><subject>Serology</subject><subject>spiralis</subject><subject>Suspension array</subject><subject>Swine</subject><subject>Swine Diseases - blood</subject><subject>Swine Diseases - diagnosis</subject><subject>Swine Diseases - parasitology</subject><subject>Trichinella - isolation & purification</subject><subject>Trichinella spiralis</subject><subject>Trichinellosis - blood</subject><subject>Trichinellosis - diagnosis</subject><subject>Trichinellosis - parasitology</subject><subject>Trichinellosis - veterinary</subject><subject>trichinosis</subject><subject>virus</subject><subject>Zoonosis</subject><issn>1090-0233</issn><issn>1532-2971</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNkUtv1TAQhSMEoqXwB1iAl93kYo8dO0ZsqoqXVAkJ2rXl-HHrq1w72Emr_nscUlgiFvZYo2-Ozvg0zWuCdwQT_u6wm-8O4w4wgdrYYZBPmlPSUWhBCvK0vrHELQZKT5oXpRwwxpIxeN6cACVCdFSeNt8v0OC0bQddnEVlKZOLJaSIdM76AfmU0XzrUHE5jWkfjB6RdbMz88okj65zMLchunHUKEQ0hX152Tzzeizu1WM9a24-fby-_NJeffv89fLiqjWMs7ntvMSWccpBghESRC-8xY55T6uzwQrvvYaeec45I5Ya4gdtO6x7bARnPT1r3m-693rvYoj1UlFnE4pKOqgxDFnnB3W_ZBXHtUzLUBRjmAtZh8-34Smnn4srszqGYtY1oktLUYRJ4IB7-A-UippAB9BVFDbU5FRKdl5NORxXFwSrNTN1UGtmas1s7eHf-m8e9Zfh6OzfkT8hVeDtBnidlN7nuuDNj6rQ4XpAcFKJDxvh6n_fBZdVMcFF42zINStlU_iXg1_fE7IJ</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>van der Wal, F.J.</creator><creator>Achterberg, R.P.</creator><creator>Kant, A.</creator><creator>Maassen, C.B.M.</creator><general>Elsevier Ltd</general><scope>FBQ</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>7X8</scope><scope>F1W</scope><scope>H95</scope><scope>H98</scope><scope>L.G</scope><scope>QVL</scope></search><sort><creationdate>20130601</creationdate><title>A bead-based suspension array for the serological detection of Trichinella in pigs</title><author>van der Wal, F.J. ; Achterberg, R.P. ; Kant, A. ; Maassen, C.B.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-5f90d4636292c792787fd0e4ff3539bd7fffa284f66641d3c1fbad50a80c76483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>antibodies</topic><topic>antigens</topic><topic>blood serum</topic><topic>enzyme-linked immunosorbent assay</topic><topic>Enzyme-Linked Immunosorbent Assay - veterinary</topic><topic>farms</topic><topic>Human</topic><topic>humans</topic><topic>immunoassay</topic><topic>Indexing in process</topic><topic>linked-immunosorbent-assay</topic><topic>multiplexed luminex assay</topic><topic>nonstructural proteins</topic><topic>Pig</topic><topic>Sensitivity and Specificity</topic><topic>serodiagnosis</topic><topic>Serologic Tests - veterinary</topic><topic>Serology</topic><topic>spiralis</topic><topic>Suspension array</topic><topic>Swine</topic><topic>Swine Diseases - blood</topic><topic>Swine Diseases - diagnosis</topic><topic>Swine Diseases - parasitology</topic><topic>Trichinella - isolation & purification</topic><topic>Trichinella spiralis</topic><topic>Trichinellosis - blood</topic><topic>Trichinellosis - diagnosis</topic><topic>Trichinellosis - parasitology</topic><topic>Trichinellosis - veterinary</topic><topic>trichinosis</topic><topic>virus</topic><topic>Zoonosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van der Wal, F.J.</creatorcontrib><creatorcontrib>Achterberg, R.P.</creatorcontrib><creatorcontrib>Kant, A.</creatorcontrib><creatorcontrib>Maassen, C.B.M.</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>NARCIS:Publications</collection><jtitle>The veterinary journal (1997)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van der Wal, F.J.</au><au>Achterberg, R.P.</au><au>Kant, A.</au><au>Maassen, C.B.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A bead-based suspension array for the serological detection of Trichinella in pigs</atitle><jtitle>The veterinary journal (1997)</jtitle><addtitle>Vet J</addtitle><date>2013-06-01</date><risdate>2013</risdate><volume>196</volume><issue>3</issue><spage>439</spage><epage>444</epage><pages>439-444</pages><issn>1090-0233</issn><eissn>1532-2971</eissn><abstract>The feasibility of using bead-based suspension arrays to detect serological evidence of Trichinella in pigs was assessed. Trichinella spiralis excretory–secretory antigen was covalently coupled to paramagnetic beads and used to bind serum antibodies, which were subsequently detected using anti-swine antibody. The assay was evaluated by testing pig sera from farms where trichinellosis was endemic and comparing the results with those obtained using two commercially available ELISAs. With cut-offs established by receiver operating characteristic (ROC) analysis, digestion-negative sera from a Trichinella-free population of pigs were deemed seronegative. When anti-swine antibody was replaced with protein A/G, higher test sensitivity (94% vs. 88%) at similar test specificity (95%), was achieved. The potential use of this assay in species other than swine was also demonstrated by testing human sera.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>23177539</pmid><doi>10.1016/j.tvjl.2012.10.029</doi><tpages>6</tpages></addata></record> |
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source | ScienceDirect Freedom Collection |
subjects | Animals antibodies antigens blood serum enzyme-linked immunosorbent assay Enzyme-Linked Immunosorbent Assay - veterinary farms Human humans immunoassay Indexing in process linked-immunosorbent-assay multiplexed luminex assay nonstructural proteins Pig Sensitivity and Specificity serodiagnosis Serologic Tests - veterinary Serology spiralis Suspension array Swine Swine Diseases - blood Swine Diseases - diagnosis Swine Diseases - parasitology Trichinella - isolation & purification Trichinella spiralis Trichinellosis - blood Trichinellosis - diagnosis Trichinellosis - parasitology Trichinellosis - veterinary trichinosis virus Zoonosis |
title | A bead-based suspension array for the serological detection of Trichinella in pigs |
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