{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,8,28]],"date-time":"2024-08-28T17:52:15Z","timestamp":1724867535306},"reference-count":13,"publisher":"American Society for Microbiology","issue":"12","license":[{"start":{"date-parts":[[2010,12,1]],"date-time":"2010-12-01T00:00:00Z","timestamp":1291161600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Clin Microbiol"],"published-print":{"date-parts":[[2010,12]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:p>\n            Practical detection of cholera toxin (CT) by a liposome PCR (LPCR) immunoassay was compared to that of an established\n            <jats:italic>V. cholerae<\/jats:italic>\n            enterotoxin and\n            <jats:italic>Escherichia coli<\/jats:italic>\n            heat-labile enterotoxin reversed passive latex agglutination (VET-RPLA) assay. LPCR detected CT in the range of 10 pg\/ml to 100 ng\/ml in simulated feces and environmental water. Detection by VET-RPLA required at least 4 to 19 ng\/ml CT.\n          <\/jats:p>","DOI":"10.1128\/jcm.02019-10","type":"journal-article","created":{"date-parts":[[2010,10,21]],"date-time":"2010-10-21T02:33:08Z","timestamp":1287628388000},"page":"4620-4622","update-policy":"http:\/\/dx.doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":6,"title":["The Liposome PCR Assay Is More Sensitive than the\n            <i>Vibrio cholerae<\/i>\n            Enterotoxin and\n            <i>Escherichia coli<\/i>\n            Heat-Labile Enterotoxin Reversed Passive Latex Agglutination Test at Detecting Cholera Toxin in Feces and Water"],"prefix":"10.1128","volume":"48","author":[{"given":"David L.","family":"Evers","sequence":"first","affiliation":[{"name":"Department of Biophysics, Armed Forces Institute of Pathology, Washington, DC"},{"name":"Biomedical Laboratory Research and Development Service, Department of Veterans Affairs, Washington, DC 20420"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Junkun","family":"He","sequence":"additional","affiliation":[{"name":"Department of Biophysics, Armed Forces Institute of Pathology, Washington, DC"},{"name":"Biomedical Laboratory Research and Development Service, Department of Veterans Affairs, Washington, DC 20420"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jeffrey T.","family":"Mason","sequence":"additional","affiliation":[{"name":"Department of Biophysics, Armed Forces Institute of Pathology, Washington, DC"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Timothy J.","family":"O'Leary","sequence":"additional","affiliation":[{"name":"Biomedical Laboratory Research and Development Service, Department of Veterans Affairs, Washington, DC 20420"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"235","reference":[{"key":"e_1_3_2_2_2","doi-asserted-by":"publisher","DOI":"10.1128\/jcm.28.1.128-130.1990"},{"key":"e_1_3_2_3_2","doi-asserted-by":"publisher","DOI":"10.1093\/infdis\/125.1.36"},{"key":"e_1_3_2_4_2","unstructured":"Food and Drug Administration. 2001. 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