A biomarker for the identification of swine fecal pollution in water, using the STII toxin gene from enterotoxigenic Escherichia coli
This research developed a PCR method to identify swine fecal pollution in water, using a portion of the STII toxin gene from enterotoxigenic Escherichia coli as the target sequence. This method showed the gene to have a wide-spread geographical distribution and temporal stability; and the primers de...
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description | This research developed a PCR method to identify swine fecal pollution in water, using a portion of the STII toxin gene from enterotoxigenic Escherichia coli as the target sequence. This method showed the gene to have a wide-spread geographical distribution and temporal stability; and the primers demonstrated high specificity, sensitivity, and reliability. A total of 110 DNA extracts from different animal fecal and human sewage samples were screened using the primers and no positives resulted. Centrifugation and filtration methods for concentrating E. coli seeded into stream, ocean, secondary effluent, and dairy lagoon waters resulted in detection limits at the femtogram and attogram levels. E. coli with the biomarker seeded into stream, ocean, and secondary effluent waters remained stable for approximately 2 weeks for all water types. Of the farm lagoon and waste samples tested, 94% were positive for the STII trait, regardless of the number of E. coli screened and 100% were positive when > or =35 E. coli isolates were screened. As the PCR product of the target sequence yielded a single band, the method is applicable to dot blot detection methodology, yielding great accuracy in determining the presence of swine fecal sources. |
doi_str_mv | 10.1007/s00253-003-1373-9 |
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A ; TSAI, Y. L ; OLSON, B. H</creator><creatorcontrib>KHATIB, L. A ; TSAI, Y. L ; OLSON, B. H</creatorcontrib><description>This research developed a PCR method to identify swine fecal pollution in water, using a portion of the STII toxin gene from enterotoxigenic Escherichia coli as the target sequence. This method showed the gene to have a wide-spread geographical distribution and temporal stability; and the primers demonstrated high specificity, sensitivity, and reliability. A total of 110 DNA extracts from different animal fecal and human sewage samples were screened using the primers and no positives resulted. Centrifugation and filtration methods for concentrating E. coli seeded into stream, ocean, secondary effluent, and dairy lagoon waters resulted in detection limits at the femtogram and attogram levels. E. coli with the biomarker seeded into stream, ocean, and secondary effluent waters remained stable for approximately 2 weeks for all water types. Of the farm lagoon and waste samples tested, 94% were positive for the STII trait, regardless of the number of E. coli screened and 100% were positive when > or =35 E. coli isolates were screened. As the PCR product of the target sequence yielded a single band, the method is applicable to dot blot detection methodology, yielding great accuracy in determining the presence of swine fecal sources.</description><identifier>ISSN: 0175-7598</identifier><identifier>EISSN: 1432-0614</identifier><identifier>DOI: 10.1007/s00253-003-1373-9</identifier><identifier>PMID: 13680204</identifier><identifier>CODEN: AMBIDG</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Animals ; Bacteria ; Bacterial Toxins - genetics ; Bacteriological methods and techniques used in bacteriology ; Bacteriology ; Biological and medical sciences ; Biomarkers ; Centrifugation ; Detection limits ; DNA Primers ; E coli ; Enterotoxins - genetics ; Environmental Monitoring ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - isolation & purification ; Escherichia coli - metabolism ; Escherichia coli Proteins ; Fecal coliforms ; Feces ; Feces - microbiology ; Fundamental and applied biological sciences. Psychology ; Geographical distribution ; Humans ; Microbiology ; Polymerase Chain Reaction ; Sensitivity and Specificity ; Sewage ; Swine ; Swine - microbiology ; Toxins ; Water Pollution</subject><ispartof>Applied microbiology and biotechnology, 2003-12, Vol.63 (2), p.231-238</ispartof><rights>2004 INIST-CNRS</rights><rights>Springer-Verlag 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-93bb1f45999c2ad2a16b881c3b6c94ca67991ff6d2fed79c3c99130d9b0389043</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15512267$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/13680204$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KHATIB, L. A</creatorcontrib><creatorcontrib>TSAI, Y. L</creatorcontrib><creatorcontrib>OLSON, B. H</creatorcontrib><title>A biomarker for the identification of swine fecal pollution in water, using the STII toxin gene from enterotoxigenic Escherichia coli</title><title>Applied microbiology and biotechnology</title><addtitle>Appl Microbiol Biotechnol</addtitle><description>This research developed a PCR method to identify swine fecal pollution in water, using a portion of the STII toxin gene from enterotoxigenic Escherichia coli as the target sequence. This method showed the gene to have a wide-spread geographical distribution and temporal stability; and the primers demonstrated high specificity, sensitivity, and reliability. A total of 110 DNA extracts from different animal fecal and human sewage samples were screened using the primers and no positives resulted. Centrifugation and filtration methods for concentrating E. coli seeded into stream, ocean, secondary effluent, and dairy lagoon waters resulted in detection limits at the femtogram and attogram levels. E. coli with the biomarker seeded into stream, ocean, and secondary effluent waters remained stable for approximately 2 weeks for all water types. Of the farm lagoon and waste samples tested, 94% were positive for the STII trait, regardless of the number of E. coli screened and 100% were positive when > or =35 E. coli isolates were screened. As the PCR product of the target sequence yielded a single band, the method is applicable to dot blot detection methodology, yielding great accuracy in determining the presence of swine fecal sources.</description><subject>Animals</subject><subject>Bacteria</subject><subject>Bacterial Toxins - genetics</subject><subject>Bacteriological methods and techniques used in bacteriology</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Centrifugation</subject><subject>Detection limits</subject><subject>DNA Primers</subject><subject>E coli</subject><subject>Enterotoxins - genetics</subject><subject>Environmental Monitoring</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - isolation & purification</subject><subject>Escherichia coli - metabolism</subject><subject>Escherichia coli Proteins</subject><subject>Fecal coliforms</subject><subject>Feces</subject><subject>Feces - microbiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Geographical distribution</subject><subject>Humans</subject><subject>Microbiology</subject><subject>Polymerase Chain Reaction</subject><subject>Sensitivity and Specificity</subject><subject>Sewage</subject><subject>Swine</subject><subject>Swine - microbiology</subject><subject>Toxins</subject><subject>Water Pollution</subject><issn>0175-7598</issn><issn>1432-0614</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkcFO3DAQhi1UBFvgAXqprErticCMnTjxESFoV0LiAJwtx7FZ02y8tRNRHoD3xmFXQuI0mpnv_zWan5BvCGcIUJ8nAFbxAoAXyGteyD2ywJKzAgSWX8gCsK6KupLNIfma0hMAskaIA3KIXDTAoFyQ1wva-rDW8a-N1IVIx5WlvrPD6J03evRhoMHR9OwHS501uqeb0PfT-8IP9FmPNp7SKfnh8V17d79c0jH8z7tHO2tiWNNsZ2OYp3nmDb1KZmWjNyuvqQm9Pyb7TvfJnuzqEXm4vrq__FPc3P5eXl7cFKZsmrGQvG3RlZWU0jDdMY2ibRo0vBVGlkaLWkp0TnTM2a6Whpvcc-hkC7yRUPIj8mvru4nh32TTqNY-Gdv3erBhSgplLWTFZQZ_fAKfwhSHfJsSDJlgsoIM4RYyMaQUrVOb6PMrXxSCmgNS24BUDkjNAanZ-PvOeGrXtvtQ7BLJwM8doFP-tot6MD59cFWFjImavwFxM5k8</recordid><startdate>20031201</startdate><enddate>20031201</enddate><creator>KHATIB, L. 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A</au><au>TSAI, Y. L</au><au>OLSON, B. H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A biomarker for the identification of swine fecal pollution in water, using the STII toxin gene from enterotoxigenic Escherichia coli</atitle><jtitle>Applied microbiology and biotechnology</jtitle><addtitle>Appl Microbiol Biotechnol</addtitle><date>2003-12-01</date><risdate>2003</risdate><volume>63</volume><issue>2</issue><spage>231</spage><epage>238</epage><pages>231-238</pages><issn>0175-7598</issn><eissn>1432-0614</eissn><coden>AMBIDG</coden><abstract>This research developed a PCR method to identify swine fecal pollution in water, using a portion of the STII toxin gene from enterotoxigenic Escherichia coli as the target sequence. This method showed the gene to have a wide-spread geographical distribution and temporal stability; and the primers demonstrated high specificity, sensitivity, and reliability. A total of 110 DNA extracts from different animal fecal and human sewage samples were screened using the primers and no positives resulted. Centrifugation and filtration methods for concentrating E. coli seeded into stream, ocean, secondary effluent, and dairy lagoon waters resulted in detection limits at the femtogram and attogram levels. E. coli with the biomarker seeded into stream, ocean, and secondary effluent waters remained stable for approximately 2 weeks for all water types. Of the farm lagoon and waste samples tested, 94% were positive for the STII trait, regardless of the number of E. coli screened and 100% were positive when > or =35 E. coli isolates were screened. As the PCR product of the target sequence yielded a single band, the method is applicable to dot blot detection methodology, yielding great accuracy in determining the presence of swine fecal sources.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>13680204</pmid><doi>10.1007/s00253-003-1373-9</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Bacteria Bacterial Toxins - genetics Bacteriological methods and techniques used in bacteriology Bacteriology Biological and medical sciences Biomarkers Centrifugation Detection limits DNA Primers E coli Enterotoxins - genetics Environmental Monitoring Escherichia coli Escherichia coli - genetics Escherichia coli - isolation & purification Escherichia coli - metabolism Escherichia coli Proteins Fecal coliforms Feces Feces - microbiology Fundamental and applied biological sciences. Psychology Geographical distribution Humans Microbiology Polymerase Chain Reaction Sensitivity and Specificity Sewage Swine Swine - microbiology Toxins Water Pollution |
title | A biomarker for the identification of swine fecal pollution in water, using the STII toxin gene from enterotoxigenic Escherichia coli |
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