Article
Foot and mouth disease virus polyepitope protein produced in bacteria and plants induces protective immunity in guinea pigs.
Bioengineering Center, Russian Academy of Sciences, Moscow, Russia.
Biochemistry (Moscow) (impact factor:
1.06).
03/2011;
76(3):339-46.
pp.339-46
Source: PubMed
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Citations (0)
- Cited In (3)
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Article: Immunoglobulin genomics in the guinea pig (Cavia porcellus).
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ABSTRACT: In science, the guinea pig is known as one of the gold standards for modeling human disease. It is especially important as a molecular and cellular biology model for studying the human immune system, as its immunological genes are more similar to human genes than are those of mice. The utility of the guinea pig as a model organism can be further enhanced by further characterization of the genes encoding components of the immune system. Here, we report the genomic organization of the guinea pig immunoglobulin (Ig) heavy and light chain genes. The guinea pig IgH locus is located in genomic scaffolds 54 and 75, and spans approximately 6,480 kb. 507 V(H) segments (94 potentially functional genes and 413 pseudogenes), 41 D(H) segments, six J(H) segments, four constant region genes (μ, γ, ε, and α), and one reverse δ remnant fragment were identified within the two scaffolds. Many V(H) pseudogenes were found within the guinea pig, and likely constituted a potential donor pool for gene conversion during evolution. The Igκ locus mapped to a 4,029 kb region of scaffold 37 and 24 is composed of 349 V(κ) (111 potentially functional genes and 238 pseudogenes), three J(κ) and one C(κ) genes. The Igλ locus spans 1,642 kb in scaffold 4 and consists of 142 V(λ) (58 potentially functional genes and 84 pseudogenes) and 11 J(λ) -C(λ) clusters. Phylogenetic analysis suggested the guinea pig's large germline V(H) gene segments appear to form limited gene families. Therefore, this species may generate antibody diversity via a gene conversion-like mechanism associated with its pseudogene reserves.PLoS ONE 01/2012; 7(6):e39298. · 4.09 Impact Factor -
Article: The use of transient expression systems for the rapid production of virus-like particles in plants.
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ABSTRACT: Advances in transient expression technologies have allowed the production of milligram quantities of proteins within a matter of days using only small amounts (tens of grams) of plant tissue. Among the proteins that have been produced using this approach are the structural proteins of viruses which are capable of forming virus-like particles (VLPs). As such particulate structures are potent stimulators of the immune system, they are excellent vaccine candidates both in their own right and as carriers of additional immunogenic sequences. VLPs of varying complexity derived from a variety of animal viruses have been successfully transiently expressed in plants and their immunological properties assessed. Generally, the plant-produced VLPs were found to have the expected antigenicity and immunogenicity. In several cases, including an M2e-based influenza vaccine candidate, the plant-expressed VLPs have been shown to be capable of stimulating protective immunity. These findings raise the prospect that low-cost plant-produced vaccines could be developed for both veterinary and human use.Current pharmaceutical design 02/2013; · 4.41 Impact Factor -
Dataset: The Use of Transient Expression Systems for the Rapid Production of Virus-like Par- ticles in Plants
[show abstract] [hide abstract]
ABSTRACT: Advances in transient expression technologies have allowed the production of milligram quantities of proteins within a matter of days using only small amounts (tens of grams) of plant tissue. Among the proteins that have been produced using this approach are the structural proteins of viruses which are capable of forming virus-like particles (VLPs). As such particulate structures are potent stimula-tors of the immune system, they are excellent vaccine candidates both in their own right and as carriers of additional immunogenic se-quences. VLPs of varying complexity derived from a variety of animal viruses have been successfully transiently expressed in plants and their immunological properties assessed. Generally, the plant-produced VLPs were found to have the expected antigenicity and immuno-genicity. In several cases, including an M2e-based influenza vaccine candidate, the plant-expressed VLPs have been shown to be capable of stimulating protective immunity. These findings raise the prospect that low-cost plant-produced vaccines could be developed for both veterinary and human use.-like particle, hepatitis B core antigen, human papillomavirus, bovine papillomavirus, bluetongue vi-rus, foot-and-mouth disease virus, influenza virus, porcine respiratory and reproductive syndrome virus, protective immunity.
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Keywords
alternative foot
E. coli bacteria
efficient immune response
efficient viral epitopes
encodes B-cell epitopes
guinea pigs
H-PE
H-PE proteins
mouth disease
mouth disease virus
N. benthamiana plants
new recombinant vaccine
phytovirus expression system
polyepitope protein
polyepitope protein H-PE
proteins 2C
proteins VP1
purified H-PE proteins induced
recombinant protein