2009
DOI: 10.2478/s11756-009-0203-7
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Heterologous expression of synthetic chicken IFN-γ in transgenic tobacco plants

Abstract: To develop a plant expression system for the production of the chicken interferon gamma (ChIFN-γ) oral vaccine adjuvant, we investigated whether the ChIFN-γ protein can be expressed in tobacco plants. The coding sequence of the ChIFN-γ gene was optimized by modification of codon usage to that of tobacco plant genes. A synthetic ChIFN-γ gene was inserted into plasmid pSW-IFNG containing the CaMV35S promoter, NOS terminator, GUS (β-glucuronidase) reporter gene and the nptII resistance gene. The synthetic ChIFN-γ… Show more

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Cited by 15 publications
(12 citation statements)
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“…Although, at the beginning of IFN therapy bovine IFN-c was used even to treat human beings, nowadays physicians and veterinary surgeons prefer to use the IFNs specific for human or animal species (Chen et al 2004;Wu et al 2009;Jalali et al 2010). Perhaps it explains our results demonstrating relatively weak effect of the plant-made bovine IFN-c on laboratory mice IgG (Fig.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Although, at the beginning of IFN therapy bovine IFN-c was used even to treat human beings, nowadays physicians and veterinary surgeons prefer to use the IFNs specific for human or animal species (Chen et al 2004;Wu et al 2009;Jalali et al 2010). Perhaps it explains our results demonstrating relatively weak effect of the plant-made bovine IFN-c on laboratory mice IgG (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…This restriction has been removed with the advent of genetically engineered organisms to produce recombinant proteins. Recombinant human IFNs have been produced in bacteria and yeast, in insect and mammalian cell cultures, and in several plant species (Wu et al 2002(Wu et al , 2008(Wu et al , 2009Chen et al 2004;Sharma 2009;Jalali et al 2010;Sirko et al 2011).…”
Section: Introductionmentioning
confidence: 99%
“…Each system has its advantages and limitations and the method of choice is largely depending on what kind of fish vaccines are to be expressed, as briefly described in Table 2. To date, both food and non-food crops (especially tobacco plant) have been used for the development of a number of animal vaccines, such as a poultry vaccine against Newcastle disease (Hahn et al 2007; Yang et al 2007; Li et al 2007; Gómez et al2009; Van Eck and Keen 2009; Wu et al 2009: for reviews see Floss et al 2007 and He et al 2008), rabies (Ashraf et al 2005; Loza-Rubio et al 2008; Roy et al 2010; Loza-Rubio et al 2012), Porcine reproductive and respiratory syndrome virus (PRRSV) and Porcine post-weaning diarrhea in piglets (Chen and Liu 2011; Kolotilin et al 2012). The vaccine against Newcastle disease was the first plant-made animal vaccine receiving regulatory approval from the US Department of Agriculture (USDA) Center for Veterinary Biologics in 2006 (www.thepoultrysite.com/poultrynews/8949/usda-issues-license-for-plant-cell-producednewcastle-disease-vaccine-for-chickens; Joensuu et al 2008).…”
Section: Exploitation Of Plant Genetic Engineering For Low Cost Produmentioning
confidence: 99%
“…Production of the Hu-IFN-γ from yeast and mammalian cells is expensive, which can limit the use of this drug in developing countries. Plants are known to act as bioreactors that might be a successful and economical means for the production of recombinant proteins (13,22). Plants as a host system have several advantages over industrial systems, such as higher biological activity, high gene expression, high production of recombinant proteins, greater stability, safety against human-animal diseases for instance HCV, HIV etc (14,21).…”
Section: Introductionmentioning
confidence: 99%