Acta Vet. Brno 2017, 86: 11-17

https://doi.org/10.2754/avb201786010011

Expression and diagnostic use of recombinant M protein of the porcine reproductive and respiratory syndrome virus

Jitka Frölichová1, Dobromila Molinková1,2, Markéta Sedlinská3, Vladimír Celer1,2

1University of Veterinary and Pharmaceutical Sciences Brno, Faculty of Veterinary Medicine, Department of Infectious Diseases and Microbiology, Brno, Czech Republic
2CEITEC – Central European Institute of Technology, Brno, Czech Republic
3University of Veterinary and Pharmaceutical Sciences Brno, Faculty of Veterinary Medicine, Clinic of Horse Diseases, Brno, Czech Republic

Received August 15, 2016
Accepted January 26, 2017

Matrix M protein combined with nucleocapsid N protein could be a promising combination of virus antigens for diagnosing the porcine reproductive and respiratory syndrome. The goal of this work was to express the recombinant M protein of the porcine reproductive and respiratory syndrome virus in Escherichia coli cells and compare its serological reactivity with the N protein of the virus. The gene coding for the M protein was cloned into the pDest17 vector. The resulting protein was purified by metalochelating affinity chromatography. Recombinant M protein was applied as an antigen in immunoblot test and compared on a panel of porcine sera with N protein based IDEXX test. Of 120 examined samples, the majority (78.3%) gave identical results using both compared tests. From the group of discrepant results, IDEXX test identified considerably more positive sera (17.5%) than M protein based test (4.2%). The main contribution of the work is finding that although IDEXX test proved to be more sensitive than M protein based test, 4.2% of sera would escape detection by serological test based on N protein. Further development and purification of the M protein for the use in Enzyme Linked Immunosorbent Assay format test could increase the performance of serological testing.

Funding

This work was supported by the Grant Agency of the Ministry of Education, Youth and Sports of the Czech Republic, COST grant no. LD12001; Internal Grant Agency of VFU Brno No. 107/2015/FVL; and by project QJ1210120 funded by National Agency for Agricultural Research (NAZV).

References

18 live references