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Structure analysis of capsid protein of Porcine circovirus type 2 from pigs with systemic disease.

Authors :
Gava D
Serrão VHB
Fernandes LT
Cantão ME
Ciacci-Zanella JR
Morés N
Schaefer R
Source :
Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] [Braz J Microbiol] 2018 Apr - Jun; Vol. 49 (2), pp. 351-357. Date of Electronic Publication: 2017 Nov 08.
Publication Year :
2018

Abstract

Economic losses with high mortality rate associated with Porcine circovirus type 2 (PCV2) is reported worldwide. PCV2 commercial vaccine was introduced in 2006 in U.S. and in 2008 in Brazil. Although PCV2 vaccines have been widely used, cases of PCV2 systemic disease have been reported in the last years. Eleven nursery or fattening pigs suffering from PCV2 systemic disease were selected from eight PCV2-vaccinated farms with historical records of PCV2 systemic disease in Southern Brazil. PCV2 genomes were amplified and sequenced from lymph node samples of selected pigs. The comparison among the ORF2 amino acid sequences of PCV2 isolates revealed three amino acid substitutions in the positions F57I, N178S and A190T, respectively. Using molecular modeling, a structural model for the capsid protein of PCV2 was built. Afterwards, the mutated residues positions were identified in the model. The structural analysis of the mutated residues showed that the external residue 190 is close to an important predicted region for antibodies recognition. Therefore, changes in the viral protein conformation might lead to an inefficient antibody binding and this could be a relevant mechanism underlying the recent vaccine failures observed in swine farms in Brazil.<br /> (Copyright © 2017 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda. All rights reserved.)

Details

Language :
English
ISSN :
1678-4405
Volume :
49
Issue :
2
Database :
MEDLINE
Journal :
Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]
Publication Type :
Academic Journal
Accession number :
29128395
Full Text :
https://doi.org/10.1016/j.bjm.2017.08.007