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Promising multiple-epitope recombinant vaccine against foot-and-mouth disease virus type O in swine.


ABSTRACT: In order to develop a completely safe immunogen to replace the traditional inactivated vaccine, a tandem-repeat multiple-epitope recombinant vaccine against foot-and-mouth disease (FMD) virus (FMDV) type O was developed. It contained three copies each of residues 141 to 160 and 200 to 213 of VP1 of the O/China/99 strain of FMDV coupled with a swine immunoglobulin G heavy-chain constant region (scIgG). The data showed that the multiple-epitope recombinant vaccine elicited high titers of anti-FMDV specific antibodies in swine at 30 days postvaccination (dpv) and conferred complete protection against a challenge with 10³ 50% swine infective doses of the O/China/99 strain. The anti-FMDV specific antibody titers were not significantly different between the multiple-epitope recombinant vaccine and the traditional vaccine (t test, P > 0.05). The number of 50% pig protective doses was 6.47, which is higher than the number recommended by the World Organization for Animal Health. The multiple-epitope recombinant vaccine resulted in a duration of immunity of at least 6 months. We speculate that the multiple-epitope recombinant vaccine is a promising vaccine that may replace the traditional inactivated vaccine for the prevention and control of FMD in swine in the future.

SUBMITTER: Shao JJ 

PROVIDER: S-EPMC3019777 | biostudies-literature | 2011 Jan

REPOSITORIES: biostudies-literature

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Promising multiple-epitope recombinant vaccine against foot-and-mouth disease virus type O in swine.

Shao Jun-Jun JJ   Wong Chung Kai CK   Lin Tong T   Lee Shuk Kwan SK   Cong Guo-Zheng GZ   Sin Fion Wai Yee FW   Du Jun-Zheng JZ   Gao Shan-Dian SD   Liu Xiang-Tao XT   Cai Xue-Peng XP   Xie Yong Y   Chang Hui-Yun HY   Liu Ji-Xing JX  

Clinical and vaccine immunology : CVI 20101117 1


In order to develop a completely safe immunogen to replace the traditional inactivated vaccine, a tandem-repeat multiple-epitope recombinant vaccine against foot-and-mouth disease (FMD) virus (FMDV) type O was developed. It contained three copies each of residues 141 to 160 and 200 to 213 of VP1 of the O/China/99 strain of FMDV coupled with a swine immunoglobulin G heavy-chain constant region (scIgG). The data showed that the multiple-epitope recombinant vaccine elicited high titers of anti-FMDV  ...[more]

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