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Journal of Biochemistry 2004 136(6):795-804; doi:10.1093/jb/mvh189
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© 2004 The Japanese Biochemical Society

BIOCHEMISTRY

Identification of Antigenic Regions of the Erns Protein for Pig Antibodies Elicited during Classical Swine Fever Virus Infection

Min Lin1,*, Erin Trottier1, John Pasick2 and Marta Sabara2

1 Animal Diseases Research Institute, Nepean, Ontario, Canada K2H 8P9; and 2 National Centre for Foreign Animal Disease, Winnipeg, Manitoba, Canada R3E 3M4

The structural glycoprotein Erns of classical swine fever virus (CSFV) is one of the major antibody targets upon infection of pigs with the virus. Molecular dissection of the structure of Erns would define the minimal immunodominant regions that induce antibody responses after infection and may thus help design an effective diagnostic reagent or vaccine. In this study, deletion analysis was made within amino acids (aa) 297 to 776 of the CSFV Alfort/187 polyprotein containing the large C-terminal portion of the Erns protein (aa 27 to 227), the entire E1 protein (aa 1 to 195), and the N-terminal portion of the E2 protein (aa 1 to 87). Various protein fragments with target deletions from N- or/and C-terminal ends were constructed with pET30, expressed in Escherichia coli and probed on Western blots with antisera from pigs infected with CSFV. This has resulted in the identification within Erns of three overlapping antigenic regions: AR1(Ernsaa 65–145), AR2 (Ernsaa 84–160 ) and AR3 (Ernsaa 109–220). N- or C-terminal deletions as small as 3 residues introduced into these regions disrupt their reactivity with antibodies, indicating that they are the minimum requirements for recognition by pig antibodies. The three minimal antigenic regions correlated well with the hydropathy profiles and the 3D structural model of Erns. Each individual region and a protein fragment containing AR1, AR2 and AR3 reacted equally well with pig anti-CSFV sera. Since variable and conserved sequences are present within the three overlapping antigenic regions of Erns of different pestiviruses, specific serological detection of CSFV infection or broad detection of pestivirus infections may be achieved with the use of a single Erns region or a combination of two or three Erns regions.

* To whom correspondence should be addressed. Tel: +1-613-228-6698, Fax: +1-613-228-6667, E-mail: linm{at}inspection.gc.ca


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M. Lin, E. Trottier, and M. Mallory
Enzyme-Linked Immunosorbent Assay Based on a Chimeric Antigen Bearing Antigenic Regions of Structural Proteins Erns and E2 for Serodiagnosis of Classical Swine Fever Virus Infection
Clin. Vaccine Immunol., July 1, 2005; 12(7): 877 - 881.
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