[Expression of multiepitope antigenic gene of Toxoplasma gondii in transgenic tomatoes]

To obtain the transgenic tomato plant expressed multiepitope antigenic gene of Toxoplasma gondii (Tg-MAG).

Tg-MAG under the control of E35S promoter, E35S-E81.1 chimeric promoter and E8 2.2 promoter in the plant expression vectors was transferred into the tomato cotyledons and hypocotyls via Agrobacterium-mediated T-DNA transformation. The candidate buds were obtained and elongated by kanamycin resistant screening. After further rooting selection, the selected tomato lines were trained and transplanted to soil and grown in a greenhouse till blossoming and bearing fruit. The transgenic tomato plants were identified using PCR, RT-PCR and Western blotting.

Tg-MAG was introduced into the transgenic plant genomic DNA and transcribed correctly at expected size 360 bp identified by PCR and RT-PCR. Western blotting results indicated that the recombinant Tg-MAG from 8 transgenic lines, expressed in tomato fruits at expected size 11900, 2 of them showed strong reaction band with HRP labeled McAb K7H3 against the major surface antigen 1( SAG1) of T. gondii tachyzoites.

Tg-MAG transgenic tomato lines were obtained. Tg-MAG recombinant protein with good immune activity was expressed successfully in transgenic tomato fruits.