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Chinese Journal of Virology ; (6): 456-461, 2011.
Article in Chinese | WPRIM | ID: wpr-354806

ABSTRACT

The objective of this study was to investigate the function of vimentin in PRRSV infection. Vimentin gene from Marc-145 cells was amplified by RT-PCR, cloned into pET-28a vector and expressed in Escherichia coli BL21(DE3). The expressed vimentin was confirmed by Western blot and purified which was used to immunize BALB/c mice for the production of antibodies. Vimentin and antibodies were tested for blocking PRRSV infection of Marc-145 cells. The binding of vimentin to PRRSV N and GP5 proteins were tested by the ELISA. The results showed that vimentin gene was amplified successfully and expressed as identified by SDS-PAGE and Western blot. Mouse anti-vimentin antibodies were produced with the titer of 10(5). PRRSV infection of Marc-145 cells was blocked partially by vimentin while blocked completely by the antibobies. In addition, vimentin was bound N protein, but not GP5. These results provide additional information on PRRSV entry into Marc-145 cells.


Subject(s)
Animals , Female , Mice , Antibodies , Allergy and Immunology , Metabolism , Cell Line , Escherichia coli , Genetics , Metabolism , Genetic Vectors , Genetics , Mice, Inbred BALB C , Porcine Reproductive and Respiratory Syndrome , Genetics , Metabolism , Virology , Porcine respiratory and reproductive syndrome virus , Physiology , Protein Binding , Physiology , Recombinant Proteins , Genetics , Allergy and Immunology , Metabolism , Swine , Vimentin , Genetics , Allergy and Immunology , Metabolism , Viral Proteins , Metabolism
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