Construction and in vivo Expression of Trichinella spralis T626-55 Gene Vaccine Carried by Attenuated Salmonella
Mingyuan Liu
Abstract
Mingyuan Liu
Abstract
Highly immunogenic gene T626-55 of Trichinella spiralis was amplified using PCR reaction and cloned into pcDNA3.1 eukaryotic expression plasmid.The recombinant plasmid was transformed into S.enterica Typhimurium phoP/phoQ strain by electroporation.In vivo expression of the target gene was testified.Mice were orally administrated with the recombinant bacteria and after 5 days of administration,spleen and Peyer′s patch were aseptically removed for reverse transcription-polymerase chain reaction(RT-PCR) and indirect fluorescence assay(IFA).The results show that Salmonella harboring T626-55 gene coding eukaryotic plasmid T626-55-pcDNA3.1-PQ was successfully constructed.The transcription of T626-55 gene was detected in spleen and pp,and expression of T626-55 protein was confirmed in spleen.
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Highly immunogenic gene T626-55 of Trichinella spiralis was amplified using PCR reaction and cloned into pcDNA3.1 eukaryotic expression plasmid.The recombinant plasmid was transformed into S.enterica Typhimurium phoP/phoQ strain by electroporation.In vivo expression of the target gene was testified.Mice were orally administrated with the recombinant bacteria and after 5 days of administration,spleen and Peyer′s patch were aseptically removed for reverse transcription-polymerase chain reaction(RT-PCR) and indirect fluorescence assay(IFA).The results show that Salmonella harboring T626-55 gene coding eukaryotic plasmid T626-55-pcDNA3.1-PQ was successfully constructed.The transcription of T626-55 gene was detected in spleen and pp,and expression of T626-55 protein was confirmed in spleen.
Key concepts: Trichinella spiralis, Molecular biology, Biology, Electroporation, Recombinant DNA, Plasmid, Gene expression, Spleen