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Significant progress has been achieved in the last 15\u00a0years, since the initial reports surfaced from <jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>ermany, <jats:styled-content style=\"fixed-case\">USA<\/jats:styled-content> and Israel of the <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>y<jats:styled-content style=\"fixed-case\">HV<\/jats:styled-content>\u20103 virus, in terms of pathology and detection. However, relatively few studies have been carried out in understanding viral replication and propagation. Antibody\u2010based affinity has been used for detection of <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>y<jats:styled-content style=\"fixed-case\">HV<\/jats:styled-content>\u20103 in enzyme\u2010linked immunosorbent assay and <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content>\u2010based techniques, and immunohistological assays have been used to describe a <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>y<jats:styled-content style=\"fixed-case\">HV<\/jats:styled-content>\u20103 membrane protein, termed <jats:styled-content style=\"fixed-case\">ORF<\/jats:styled-content>81. In this study, monoclonal antibodies linked to <jats:styled-content style=\"fixed-case\">N<\/jats:styled-content>\u2010hydroxysuccinimide (<jats:styled-content style=\"fixed-case\">NHS<\/jats:styled-content>)\u2010activated spin columns were used to purify <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>y<jats:styled-content style=\"fixed-case\">HV<\/jats:styled-content>\u20103 and host proteins from tissue samples originating in either <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>y<jats:styled-content style=\"fixed-case\">HV<\/jats:styled-content>\u20103 symptomatic or asymptomatic fish. The samples were next analysed either by polyacrylamide gel electrophoresis (<jats:styled-content style=\"fixed-case\">PAGE<\/jats:styled-content>) and subsequently by electrospray ionization coupled to mass spectrometry (<jats:styled-content style=\"fixed-case\">ESI<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MS<\/jats:styled-content>) or by <jats:styled-content style=\"fixed-case\">ESI<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MS<\/jats:styled-content> analysis directly after purification. A total of 78 host proteins and five <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>y<jats:styled-content style=\"fixed-case\">HV<\/jats:styled-content>\u20103 proteins were identified in the two analyses. These data can be used to develop novel control methods for Cy<jats:styled-content style=\"fixed-case\">HV<\/jats:styled-content>\u20103, based on pathways or proteins identified in this study.<\/jats:p>","DOI":"10.1111\/jfd.12073","type":"journal-article","created":{"date-parts":[[2013,1,24]],"date-time":"2013-01-24T15:58:46Z","timestamp":1359043126000},"page":"721-733","source":"Crossref","is-referenced-by-count":14,"title":["Antibody screening identifies 78 putative host proteins involved in <scp>C<\/scp>yprinid herpesvirus 3 infection or propagation in common carp, <i><scp>C<\/scp>yprinus carpio<\/i>\u00a0<scp>L<\/scp>"],"prefix":"10.1111","volume":"36","author":[{"given":"M","family":"Gotesman","sequence":"first","affiliation":[{"name":"Clinical Division of Fish Medicine University of Veterinary Medicine Vienna Austria"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H","family":"Soliman","sequence":"additional","affiliation":[{"name":"Clinical Division of Fish 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