A PCR technique for forensic, species-level identification of abalone tissue
Although the incidence of abalone poaching is increasing in South Africa, several alleged poachers have been acquitted in cases where the state has been unable to prove that the confiscated meat is of the local abalone, Haliotis midae. This species is illegally exported to the Far East by poaching s...
Gespeichert in:
Veröffentlicht in: | Journal of shellfish research 1998-12, Vol.17 (3), p.889-895 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 895 |
---|---|
container_issue | 3 |
container_start_page | 889 |
container_title | Journal of shellfish research |
container_volume | 17 |
creator | Sweijd, NA Bowie, RCK Lopata, AL Marinaki, A M Harley, E H Cook, P A |
description | Although the incidence of abalone poaching is increasing in South Africa, several alleged poachers have been acquitted in cases where the state has been unable to prove that the confiscated meat is of the local abalone, Haliotis midae. This species is illegally exported to the Far East by poaching syndicates, a practice that is undermining the legitimate industry. To solve this, a polymerase chain reaction (PCR) technique that targets a portion of the lysin gene of several abalone species and unequivocally distinguishes between H. midae and H. spadicea (a sympatric congeneric) has been developed. The PCR primers specifically amplify approximately 1,300 bp of genomic DNA from dried, cooked, and fresh abalone tissue. A smaller fragment of 146 bp is used for canned abalone. Restriction fragment length polymorphism (RFLP) exploit interspecific polymorphisms that discriminate between these two species. The method can also be used to identify H. rubra and can easily be adapted to other abalone species under the same threat of overexploitation. |
format | Article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_17180613</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>17180613</sourcerecordid><originalsourceid>FETCH-LOGICAL-p184t-411f7e81376d86c60d8b3d0e1450a0102520ba0d5bb02dd00f752792375e86c33</originalsourceid><addsrcrecordid>eNotjs1KxDAURrNQcBx9h6xcWbhJ2iZdDsU_KIyIroc0ucFITOrc1Od3RBcfZ3M4fGdsA1pBYwDggl0SfQDIYdDthk07_jy-8IruPcevFXkox99hpuhuOS3oIlKT8BsTjx5zjSE6W2PJvARuZ5tKRl4j0YpX7DzYRHj9zy17u797HR-baf_wNO6mZhGmrU0rRNBohNK9N73rwZtZeUDRdmBBgOwkzBZ8N88gvQcIupN6kEp3ePKV2rKbv-5yLKfPVA-fkRymZDOWlQ5CCwO9UOoHW4xJAQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17180613</pqid></control><display><type>article</type><title>A PCR technique for forensic, species-level identification of abalone tissue</title><source>Biodiversity Heritage Library</source><creator>Sweijd, NA ; Bowie, RCK ; Lopata, AL ; Marinaki, A M ; Harley, E H ; Cook, P A</creator><creatorcontrib>Sweijd, NA ; Bowie, RCK ; Lopata, AL ; Marinaki, A M ; Harley, E H ; Cook, P A</creatorcontrib><description>Although the incidence of abalone poaching is increasing in South Africa, several alleged poachers have been acquitted in cases where the state has been unable to prove that the confiscated meat is of the local abalone, Haliotis midae. This species is illegally exported to the Far East by poaching syndicates, a practice that is undermining the legitimate industry. To solve this, a polymerase chain reaction (PCR) technique that targets a portion of the lysin gene of several abalone species and unequivocally distinguishes between H. midae and H. spadicea (a sympatric congeneric) has been developed. The PCR primers specifically amplify approximately 1,300 bp of genomic DNA from dried, cooked, and fresh abalone tissue. A smaller fragment of 146 bp is used for canned abalone. Restriction fragment length polymorphism (RFLP) exploit interspecific polymorphisms that discriminate between these two species. The method can also be used to identify H. rubra and can easily be adapted to other abalone species under the same threat of overexploitation.</description><identifier>ISSN: 0730-8000</identifier><language>eng</language><subject>Haliotis midae ; Haliotis rubra ; Haliotis spadicea ; Marine</subject><ispartof>Journal of shellfish research, 1998-12, Vol.17 (3), p.889-895</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids></links><search><creatorcontrib>Sweijd, NA</creatorcontrib><creatorcontrib>Bowie, RCK</creatorcontrib><creatorcontrib>Lopata, AL</creatorcontrib><creatorcontrib>Marinaki, A M</creatorcontrib><creatorcontrib>Harley, E H</creatorcontrib><creatorcontrib>Cook, P A</creatorcontrib><title>A PCR technique for forensic, species-level identification of abalone tissue</title><title>Journal of shellfish research</title><description>Although the incidence of abalone poaching is increasing in South Africa, several alleged poachers have been acquitted in cases where the state has been unable to prove that the confiscated meat is of the local abalone, Haliotis midae. This species is illegally exported to the Far East by poaching syndicates, a practice that is undermining the legitimate industry. To solve this, a polymerase chain reaction (PCR) technique that targets a portion of the lysin gene of several abalone species and unequivocally distinguishes between H. midae and H. spadicea (a sympatric congeneric) has been developed. The PCR primers specifically amplify approximately 1,300 bp of genomic DNA from dried, cooked, and fresh abalone tissue. A smaller fragment of 146 bp is used for canned abalone. Restriction fragment length polymorphism (RFLP) exploit interspecific polymorphisms that discriminate between these two species. The method can also be used to identify H. rubra and can easily be adapted to other abalone species under the same threat of overexploitation.</description><subject>Haliotis midae</subject><subject>Haliotis rubra</subject><subject>Haliotis spadicea</subject><subject>Marine</subject><issn>0730-8000</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNotjs1KxDAURrNQcBx9h6xcWbhJ2iZdDsU_KIyIroc0ucFITOrc1Od3RBcfZ3M4fGdsA1pBYwDggl0SfQDIYdDthk07_jy-8IruPcevFXkox99hpuhuOS3oIlKT8BsTjx5zjSE6W2PJvARuZ5tKRl4j0YpX7DzYRHj9zy17u797HR-baf_wNO6mZhGmrU0rRNBohNK9N73rwZtZeUDRdmBBgOwkzBZ8N88gvQcIupN6kEp3ePKV2rKbv-5yLKfPVA-fkRymZDOWlQ5CCwO9UOoHW4xJAQ</recordid><startdate>19981201</startdate><enddate>19981201</enddate><creator>Sweijd, NA</creator><creator>Bowie, RCK</creator><creator>Lopata, AL</creator><creator>Marinaki, A M</creator><creator>Harley, E H</creator><creator>Cook, P A</creator><scope>7TN</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>P64</scope></search><sort><creationdate>19981201</creationdate><title>A PCR technique for forensic, species-level identification of abalone tissue</title><author>Sweijd, NA ; Bowie, RCK ; Lopata, AL ; Marinaki, A M ; Harley, E H ; Cook, P A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p184t-411f7e81376d86c60d8b3d0e1450a0102520ba0d5bb02dd00f752792375e86c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Haliotis midae</topic><topic>Haliotis rubra</topic><topic>Haliotis spadicea</topic><topic>Marine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sweijd, NA</creatorcontrib><creatorcontrib>Bowie, RCK</creatorcontrib><creatorcontrib>Lopata, AL</creatorcontrib><creatorcontrib>Marinaki, A M</creatorcontrib><creatorcontrib>Harley, E H</creatorcontrib><creatorcontrib>Cook, P A</creatorcontrib><collection>Oceanic Abstracts</collection><collection>Technology Research Database</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of shellfish research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sweijd, NA</au><au>Bowie, RCK</au><au>Lopata, AL</au><au>Marinaki, A M</au><au>Harley, E H</au><au>Cook, P A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A PCR technique for forensic, species-level identification of abalone tissue</atitle><jtitle>Journal of shellfish research</jtitle><date>1998-12-01</date><risdate>1998</risdate><volume>17</volume><issue>3</issue><spage>889</spage><epage>895</epage><pages>889-895</pages><issn>0730-8000</issn><abstract>Although the incidence of abalone poaching is increasing in South Africa, several alleged poachers have been acquitted in cases where the state has been unable to prove that the confiscated meat is of the local abalone, Haliotis midae. This species is illegally exported to the Far East by poaching syndicates, a practice that is undermining the legitimate industry. To solve this, a polymerase chain reaction (PCR) technique that targets a portion of the lysin gene of several abalone species and unequivocally distinguishes between H. midae and H. spadicea (a sympatric congeneric) has been developed. The PCR primers specifically amplify approximately 1,300 bp of genomic DNA from dried, cooked, and fresh abalone tissue. A smaller fragment of 146 bp is used for canned abalone. Restriction fragment length polymorphism (RFLP) exploit interspecific polymorphisms that discriminate between these two species. The method can also be used to identify H. rubra and can easily be adapted to other abalone species under the same threat of overexploitation.</abstract><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0730-8000 |
ispartof | Journal of shellfish research, 1998-12, Vol.17 (3), p.889-895 |
issn | 0730-8000 |
language | eng |
recordid | cdi_proquest_miscellaneous_17180613 |
source | Biodiversity Heritage Library |
subjects | Haliotis midae Haliotis rubra Haliotis spadicea Marine |
title | A PCR technique for forensic, species-level identification of abalone tissue |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T06%3A40%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20PCR%20technique%20for%20forensic,%20species-level%20identification%20of%20abalone%20tissue&rft.jtitle=Journal%20of%20shellfish%20research&rft.au=Sweijd,%20NA&rft.date=1998-12-01&rft.volume=17&rft.issue=3&rft.spage=889&rft.epage=895&rft.pages=889-895&rft.issn=0730-8000&rft_id=info:doi/&rft_dat=%3Cproquest%3E17180613%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17180613&rft_id=info:pmid/&rfr_iscdi=true |