Cloned viral protein vaccine for foot-and-mouth disease: responses in cattle and swine

A DNA sequence coding for the immunogenic capsid protein VP$_{3}$ of foot-and-mouth disease virus A$_{12}$, prepared from the virion RNA, was ligated to a plasmid designed to express a chimeric protein from the Escherichia coli tryptophan promoter-operator system. When Escherichia coli transformed w...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 1981-12, Vol.214 (4525), p.1125-1129
Hauptverfasser: Kleid, D.G, Yansura, D, Small, B, Dowbenko, D, Moore, D.M, Grubman, M.J, McKercher, P.D, Morgan, D.O, Robertson, B.H, Backrach, H.L
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Sprache:eng
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Zusammenfassung:A DNA sequence coding for the immunogenic capsid protein VP$_{3}$ of foot-and-mouth disease virus A$_{12}$, prepared from the virion RNA, was ligated to a plasmid designed to express a chimeric protein from the Escherichia coli tryptophan promoter-operator system. When Escherichia coli transformed with this plasmid was grown in tryptophan-depleted media, approximately 17 percent of the total cellular protein was found to be an insoluble and stable chimeric protein. The purified chimeric protein competed equally on a molar basis with VP$_{3}$ for specific antibodies to foot-and-mouth disease virus. When inoculated into six cattle and two swine, this protein elicited high levels of neutralizing antibody and protection against challenge with foot-and-mouth disease virus.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.6272395