Construction of recombinant eukaryotic expression plasmid harboring epsilon toxin gene of Clostridium perfringens and immunization studies for the development of DNA based vaccine
| dc.contributor.guide | ||
| dc.coverage.spatial | ||
| dc.creator.researcher | DESHMUKH, SACHIN KUMAR | |
| dc.date.accessioned | 2022-03-17T04:53:22Z | |
| dc.date.available | 2022-03-17T04:53:22Z | |
| dc.date.awarded | ||
| dc.date.completed | 2013 | |
| dc.date.registered | 2008 | |
| dc.description.abstract | The present study was aimed to develop a DNA based vaccine against the epsilon toxin of Clostridium perfringens which cause the fatal disease enterotoxemia in sheep. The findings of the study are summarized as follows: newlineand#61623; For the development of DNA based vaccine, PCR amplification of the gene encoding epsilon toxin was performed using gene specific primers. newlineand#61623; The epsilon toxin gene was cloned in pEGFPN-1 vector as GFP fusion and in vitro expression of epsilon toxin in CHO-K1 cells was confirmed by microscopic analysis. newlineand#61623; In another strategy for the expression of epsilon toxin in cytosolic and membrane bound form, Etx gene was PCR amplified. newlineand#61623; Epsilon toxin gene was cloned in pcDNA3.1 and pDisplay vectors for cytosolic and membrane bound expression of the protein. newlineand#61623; In vitro expression of epsilon toxin from DNA vaccine constructs (pcDNAEtx and pDSmEtx) in CHO-K1 cells was confirmed by immunoblotting using anti-Etx antisera. newlineand#61623; Mice immunized with pcDNAEtx (cytosolic) and pDSmEtx (membrane bound) DNA vaccine constructs mounted immune response against epsilon toxin. newlineand#61623; Epsilon toxin specific antibodies from the sera obtained after DNA vaccine immunized animals were able to detect epsilon toxin in western blot and ELISA. newlineand#61623; The Immunoglobulin isotyping analysis of the sera obtained by pcDNAEtx and pDSmEtx was performed and IgG1 isotype from heavy chain and Igand#1082; isotype from light chain was found to be dominant isotypes. newlineSummary newline76 newlineand#61623; No significant increase in titer was observed when mice immunized with pcDNAEtx, pDSmEtx were given 2 and 3 boosters newlineand#61623; To enhance the antibody titer different amount of immunization with higher concentration of pcDNAEtx and pDSmEtx did not show significance increase in titer. newlineand#61623; Immunization with pcDNAEtx or pDSmEtx DNA mixed with the adjuvant aluminum hydroxide did not increase the titer significantly. newlineand#61623; To analyze the efficacy of the sera obtained from DNA vaccine immunized animals to neutralize epsilon toxin in vitro, neutralization assay was performed and capacity of sera to protect MDCK ce | |
| dc.description.note | ||
| dc.format.accompanyingmaterial | DVD | |
| dc.format.dimensions | A4 | |
| dc.format.extent | 5.21MB | |
| dc.identifier.uri | http://hdl.handle.net/10603/368808 | |
| dc.language | English | |
| dc.publisher.institution | Department of Bio Technology | |
| dc.publisher.place | Bhopal | |
| dc.publisher.university | Rajiv Gandhi Proudyogiki Vishwavidyalaya | |
| dc.relation | ||
| dc.rights | university | |
| dc.source.university | University | |
| dc.subject.keyword | Engineering | |
| dc.subject.keyword | Engineering and Technology | |
| dc.subject.keyword | Engineering Biomedical | |
| dc.title | Construction of recombinant eukaryotic expression plasmid harboring epsilon toxin gene of Clostridium perfringens and immunization studies for the development of DNA based vaccine | |
| dc.title.alternative | ||
| dc.type.degree | Ph.D. |
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