Recombined prokaryotic expression detection antigen for detecting local trichina nematode antibody and producing method thereof

Abstract

The present invention provides a recombinant prokaryotic expression protein antigen for detecting autochthonous trichinella spiralis antibody and its preparation method. Said product can be used as detection antigen of indirect-ELISA and Dot-ELISA method for detecting autochthonous trichinella spiralis antibody, also can be used as gene engineering subunit vaccine for preventing autochthonous trichinella spiralis infection. The preparation process of said product includes the following steps: (1) designing specific primer for amplifying TNPG gene; (2), utilizing PCR amplification to obtain TNPG gene segment; (3), cloning TNPG gene and sequencing, and making identification; (4), directionally subcloning TNPG gene to pET-3a prokaryotic expression vector; (5), induced expression of TNPG gene in colibacillus; and (6), affinity chromatography purification of TNPG gene expression protein.

Description

technical field

[0001] The invention relates to a preparation method of a genetic engineering product, in particular to a TNPG gene recombination prokaryotic expression detection antigen protein for detecting native trichinella trichinella antibodies and its preparation method. Background technique

[0002] Trichinellosis (Trichinellosis) is an important zoonotic nematode disease caused by the adult and larvae of Trichinella spiralis infecting humans or animals. It occurs all over the world, and the local Trichinella nativa is one of its pathogens . The disease is mainly caused by eating raw or undercooked pork or other animal meat containing Trichinella cysts, and causes human death due to myocarditis and pneumonia. Because trichinella has many infected hosts, the prevalence of trichinellosis is wide and the transmission route is complicated, so this serious threat to human health is caused by animal husbandry (especially pig farming), meat industry and foreign trade expor...