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  4. Comparative studies of the capsid precursor polypeptide P1 and the capsid protein VP1 cDNA vectors for DNA vaccination against foot-and-mouth disease virus
 
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Comparative studies of the capsid precursor polypeptide P1 and the capsid protein VP1 cDNA vectors for DNA vaccination against foot-and-mouth disease virus

Resource
The Journal of Gene Medicine 7 (6): 708-717
Journal
The Journal of Gene Medicine
Pages
708-717
Date Issued
2005
Date
2005
Author(s)
Yang, Ning-Sun
Wang, Jeng-Hwan
Lin, Ku-Feng
Wang, Chien-Yu
Kim, Suk-Am
Yang, Yu-Ling
Jong, Ming-Hwa
Kuo, Tsun-Yung
Lai, Shiow-Suey
Cheng, R. Holland
Chan, Ming-Tsair
Liang, Shu-Mei
DOI
10.1002/jgm.723
URI
http://ntur.lib.ntu.edu.tw//handle/246246/162822
Abstract
Background: Foot-and-mouth disease virus (FMDV) causes a severe livestock disease, and the virus is an interesting target for virology and vaccine studies. Materials and methods: Here we evaluated comparatively three different viral antigen-encoding DNA sequences, delivered via two physical means (i.e., gene gun delivery into skin and electroporation delivery into muscle), for naked DNA-mediated vaccination in a mouse system. Results: Both methods gave similar results, demonstrating commonality of the observed DNA vaccine effects. Immunization with a cDNA vector expressing the major viral antigen (VP1) alone routinely failed to induce the production of anti-VP1 or neutralizing antibodies in test mice. As a second approach, the plasmid L-VP1 that produces a transgenic membrane-anchored VP1 protein elicited a strong antibody response, but all test mice failed in the FMDV challenge experiment. In contrast, for mice immunized with the viral capsid precursor protein (P1) cDNA expression vector, both neutralizing antibodies and 80-100% protection in test mice were detected. Conclusions: This strategy of using the whole capsid precursor protein P1 cDNA for vaccination, intentionally without the use of virus-specific protease or other encoding genes for safety reasons, may thus be employed as a relevant experimental system for induction or upgrading of effective neutralizing antibody response, and as a convenient surrogate test system for DNA vaccination studies of FMDV and presumably other viral diseases. Copyright ? 2005 John Wiley & Sons, Ltd.
Subjects
Capsid protein; DNA vaccine; FMDV; Immunogenicity; Viral clearance
SDGs

[SDGs]SDG3

Other Subjects
capsid protein; complementary DNA; DNA vaccine; neutralizing antibody; polypeptide P1; protein VP1; unclassified drug; animal experiment; animal model; article; comparative study; DNA sequence; DNA vector; electroporation; foot and mouth disease; Foot and mouth disease virus; gene expression; gene gun; immunization; in vitro study; in vivo study; mouse; nonhuman; nonviral gene delivery system; plasmid; priority journal; vaccination; Foot-and-mouth disease virus; Miridae

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