{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,12]],"date-time":"2026-02-12T11:31:06Z","timestamp":1770895866014,"version":"3.50.1"},"reference-count":25,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2014,7,4]],"date-time":"2014-07-04T00:00:00Z","timestamp":1404432000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/3.0\/"}],"funder":[{"DOI":"10.13039\/100008495","name":"Blood Systems Research Institute","doi-asserted-by":"crossref","award":["10734"],"award-info":[{"award-number":["10734"]}],"id":[{"id":"10.13039\/100008495","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100000050","name":"National Heart, Lung and Blood Institute","doi-asserted-by":"crossref","award":["HHSN268201000047C"],"award-info":[{"award-number":["HHSN268201000047C"]}],"id":[{"id":"10.13039\/100000050","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Transfusion"],"published-print":{"date-parts":[[2014,9]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p>Transfusion\u2010transmitted babesiosis caused by <jats:italic><jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>abesia microti<\/jats:italic> has emerged as a significant risk to the <jats:styled-content style=\"fixed-case\">US<\/jats:styled-content> blood supply. This study estimated the prevalence of <jats:italic><jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>.\u2009microti<\/jats:italic> antibodies in blood donors using an investigational enzyme immunoassay (<jats:styled-content style=\"fixed-case\">EIA<\/jats:styled-content>).<\/jats:p><\/jats:sec><jats:sec><jats:title>Study Design and Methods<\/jats:title><jats:p>A peptide\u2010based <jats:styled-content style=\"fixed-case\">EIA<\/jats:styled-content> that detects both immunoglobulin (<jats:styled-content style=\"fixed-case\">Ig<\/jats:styled-content>)<jats:styled-content style=\"fixed-case\">G<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">IgM<\/jats:styled-content> antibodies to <jats:italic><jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>.\u2009microti<\/jats:italic> was developed and validated. Donor samples randomly selected from areas defined as high\u2010risk endemic, lower\u2010risk endemic, and nonendemic for <jats:italic><jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>.\u2009microti<\/jats:italic> were deidentified and tested using the investigational <jats:styled-content style=\"fixed-case\">EIA<\/jats:styled-content>. Samples that were <jats:styled-content style=\"fixed-case\">EIA<\/jats:styled-content> repeat reactive were further tested by <jats:italic><jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>.\u2009microti<\/jats:italic> immunofluorescent assay (<jats:styled-content style=\"fixed-case\">IFA<\/jats:styled-content>), polymerase chain reaction (<jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content>) on red blood cell lysates, and peripheral blood smear examination. A random subset of 1272 samples from high\u2010risk endemic areas was tested by <jats:styled-content style=\"fixed-case\">IFA<\/jats:styled-content>, <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content>, and peripheral blood smear in parallel with <jats:styled-content style=\"fixed-case\">EIA<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Among 15,000 donations tested with the investigational <jats:italic><jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>.\u2009microti<\/jats:italic>\u2005<jats:styled-content style=\"fixed-case\">EIA<\/jats:styled-content>, <jats:styled-content style=\"fixed-case\">EIA<\/jats:styled-content> repeat\u2010reactive rates were 1.08% (54\/5000) in a high\u2010risk endemic area, 0.74% (37\/5000) in a lower\u2010risk area, and 0.40% (20\/5000) in a nonendemic area. After application of a revised cutoff, these values were reduced to 0.92%, (46\/5000), 0.54% (27\/5000), and 0.16% (8\/5000). Overall concordance between <jats:styled-content style=\"fixed-case\">EIA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">IFA<\/jats:styled-content> among donor samples was 99.34%. One seropositive sample was positive by <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>The seroprevalence of <jats:italic><jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>.\u2009microti<\/jats:italic> in blood donors in a high\u2010risk area measured by an investigational <jats:styled-content style=\"fixed-case\">EIA<\/jats:styled-content> was approximately 1%. The <jats:styled-content style=\"fixed-case\">EIA<\/jats:styled-content> shows promise as an efficient high\u2010throughput blood donor screening assay for <jats:italic><jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>.\u2009microti<\/jats:italic>.<\/jats:p><\/jats:sec>","DOI":"10.1111\/trf.12763","type":"journal-article","created":{"date-parts":[[2014,7,4]],"date-time":"2014-07-04T08:53:27Z","timestamp":1404464007000},"page":"2237-2244","source":"Crossref","is-referenced-by-count":38,"title":["Determination of <i><scp>B<\/scp>abesia microti<\/i> seroprevalence in blood donor populations using an investigational enzyme immunoassay"],"prefix":"10.1111","volume":"54","author":[{"given":"Andrew E.","family":"Levin","sequence":"first","affiliation":[{"name":"Immunetics, Inc.  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