High-level prokaryotic expression of envelope exterior of membrane protein of porcine epidemic diarrhea virus

Veterinary Microbiology

Volumn 123, Issue 1-3, 2007, Pages 187-193

  Shenyang, Gao ^a   Enhui, Zha ^b   Baoxian, Li ^a   Xinyuan, Qiao ^a   Lijie, Tang ^a   Junwei, Ge ^a   Yijing, Li ^a,b  

^a NORTHEAST AGRICULTURAL UNIVERSITY   (China)

^b JINZHOU MEDICAL UNIVERSITY   (China)

Author keywords

PEDV; Prokaryotic expression; Recombinant truncated M protein

Indexed keywords

VIRUS ENVELOPE PROTEIN;

ARTICLE; CONTROLLED STUDY; ENZYME LINKED IMMUNOSORBENT ASSAY; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; PORCINE EPIDEMIC DIARRHEA VIRUS; PROTEIN EXPRESSION; RNA VIRUS;

ANIMALS; CORONAVIRUS INFECTIONS; ESCHERICHIA COLI; GENE EXPRESSION; MICE; MICE, INBRED BALB C; PORCINE EPIDEMIC DIARRHEA VIRUS; RECOMBINANT PROTEINS; SWINE; SWINE DISEASES; VIRAL ENVELOPE PROTEINS; VIRAL MATRIX PROTEINS;

PORCINE EPIDEMIC DIARRHEA VIRUS; PROKARYOTA; SUS;

EID: 34250218561     PISSN: 03781135     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vetmic.2007.03.027     Document Type: Article

References (24)

1. de Haan C.A.M., Kuo L., Masters P.S., Vennema H., and Rottier P.J.M. Coronavirus particle assembly primary structure requirements of the membrane protein. J. Virol. 72 (1998) 6838-6850
2. Ducatelle R., Coussement W., Pensaert M., Debouck P., and Hoorens J. In vivo morphogenesis of a new porcine enteric coronavirus, CV777. Arch. Virol. 68 (1981) 35-44
3. Debouck P., Callebaut P., and Pensaert M. Prevalence of the porcine epidemic diarrhea (PED) virus in the pig population of different countries. Proc. Int. Pig. Vet. Soc. Congr. 7 (1982) 53
4. Egberink H.F., Ederveen J., Callebant P., and Horzinek M.C. Characterization of the structural proteins of porcine epizootic diarrhea virus, strain CV777. Am. J. Vet. Res. 49 (1988) 1320-1324
5. Guscetti F., Bernasconi C., Tobler K., Van Reeth K., Pospischil A., and Ackermann M. Immunohistochemical detection of porcine epidemic diarrhea virus compared to other methods. Clin. Diagn. Lab. Immunol. 5 (1998) 412-414
6. Gabriella E., Giuseppe F., Annamaria P., Vito M., Michele C., Francesco C., and Canio B. Recombinant M protein-based ELISA test for detection of antibodies to canine coronavirus. J. Virol. Methods 109 (2003) 139-142
7. Hofmann M., and Wyler R. Study of the occurrence of epizootic viral diarrhea in swine in Switzerland. Schweiz Arch. Tierheilkd. 129 (1987) 437-442
8. Hofmann M., and Wyler R. Enzyme-linked immunosorbent assay for the detection of porcine epidemic diarrhoea coronavirus antibodies in swine sera. Vet. Microbiol. 21 (1990) 263-273
9. Jinhui F., and Yijing L. Cloning and sequence analysis of the m gene of porcine epidemic diarrhea virus LJB/03. Virus Genes 30 (2005) 69-73
10. Jin S.Oh., Dae S.S., Yang J.-S., Ju Y.S., Yoo H.-S., Jang Y.-S., and Bong K.P. Effect of soluble porcine aminopeptidase N on antibody production against porcine epidemic diarrhea virus. J. Vet. Sci. 5 (2004) 353-357
11. Jin S.Oh., Dae S.S., Jeong S.Y., Ju Y.S., Hyoung J.M., Tae Y.K., and Bong K.P. Comparison of an enzyme-linked immunosorbent assay with serum neutralization test for serodiagnosis of porcine epidemic diarrhea virus infection. J. Vet. Sci. 6 (2005) 349-352
12. Knuchel M., Ackermann M., Muller H.K., and Kihm U. An ELISA for detection of antibodies against porcine epidemic diarrhoea virus (PEDV) based on the specific solubility of the viral surface glycoprotein. Vet. Microbiol. 32 (1992) 117-134
13. Kopecky S.A., and Lyles D.S. Constrasting effects of matrix protein on apoptosis in HeLa and BHK cells infected with vesicular stomatitis virus are due to inhibition of host gene expression. J. Virol. 77 (2003) 4658-4669
14. Kopecky S.A., Willingham M.C., and Lyles D.S. Matrix protein and another viral component contribute to induction of apoptosis in cells infected with vesicular stomatitis virus. J. Virol. 75 (2001) 12169-12181
15. Locker J.K., Rose J.K., Horzinek M.C., and Rottier P.J.M. Membrane assembly of the triple-spanning coronavirus M protein. Individual transmembrane domains show preferred orientation. J. Biol. Chem. 267 (1992) 21911-21918
16. Murphy F.A., Gibbs E.P.J., HorZinek M.C., and Studdert M.J. Veterinary Virology (1999), Cademic Press, San Diego pp. 496-501
17. Rodak L., Smid B., Nevorankova Z., Valicek L., and Smitalova R. An ELISA optimized for porcine epidemic diarrhoea virus detection in faeces. J. Vet. Microbiol. 105 (2005) 9-17
18. Rottier P.J.M. The coronavirus membrane protein. In: Siddel S.G. (Ed). The Coronaviridae (1995), Plenum Press, New York 115-139
19. Sang-Geon Y., Mercedes H., Peter J.K., and Eva N. Cloning and sequence analysis of the spike gene of porcine epidemic diarrhea virus Chinju99. Virus Genes 26 (2003) 239-246
20. Utiger A., Tobler K., Bridgen A., Suter M., Singh M., and Ackermann M. Identification of proteins specified by porcine epidemic diarrhea virus. Adv. Exp. Med. Biol. 380 (1995) 87-90
21. Utiger A., Tobler K., Bridgen A., and Ackermann M. Identification of the membrane protein of porcine epidemic diarrhea virus. Virus Genes 10 (1995) 137-148
22. Wang L.F., Gould A.R., and Selleck P.W. Expression of equine morbillivirus (EMV) matrix and fusion proteins and their evaluation as diagnostic reagents. Arch. Virol. 142 (1997) 2269-2279
23. Wood E.N. An apparently new syndrome of porcine epidemic diarrhea. Vet. Rec. 100 (1977) 243-244
24. Woods R.D., Wesley R., and Kapke P.A. Complement-dependent neutralization of transmissible gastroenteritis virus by monoclonal antibodies. Adv. Exp. Med. Biol. 218 (1987) 493-500