| Literature DB >> 22771210 |
Chao-Liang Leng1, Tong-Qing An, Jia-Zeng Chen, Da-Qing Gong, Jin-Mei Peng, Yong-Qian Yang, Jiang Wu, Juan-Juan Guo, Deng-Yun Li, Yi Zhang, Zhen-Xiang Meng, Yu-Quan Wu, Zhi-Jun Tian, Guang-Zhi Tong.
Abstract
In 2006, highly pathogenic porcine reproductive and respiratory syndrome virus (HP-PRRSV) caused great economic losses emerged in China and continues to be a threat for the pig industry. B antigenic region (AR) ((37)SHL/FQLIYNL(45)) of GP5 was considered to be a major linear neutralizing AR in PRRSV classical strains. However, peptide-purified antibodies against this AR did not neutralize PRRSV in a recent report. Compared with classical PRRSV, one amino acid mutation (L/F(39)→ I(39)) was found in B AR of HP-PRRSV. To study the ability of B AR of HP-PRRSV to induce neutralizing antibody (NA) in vitro and in vivo, rabbit antisera against B AR with and without the mutation and pig hyperimmune sera with high titer of NAs against HP-PRRSV were prepared. Immunofluorescence assays (IFA) showed that the two rabbit antisera both had reactivity to classical PRRSV CH-1a and HP-PRRSV HuN4 with no observable difference in IFA titer. However, antisera did not have neutralizing activity against classical PRRSV CH-1a and HP-PRRSV HuN4. No correlation was observed between the levels of anti-B AR peptide antibodies and NAs in pig hyperimmune sera that were detected by indirect ELISA and virus neutralization, respectively. B AR peptide-specific serum antibodies had no neutralizing activity and, GST-B fusion protein could not inhibit neutralization of NAs in pig hyperimmune sera. Based on these findings, we conclude that B AR of HP-PRRSV is not a neutralizing AR of HP-PRRSV GP5.Entities:
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Year: 2012 PMID: 22771210 DOI: 10.1016/j.vetmic.2012.06.018
Source DB: PubMed Journal: Vet Microbiol ISSN: 0378-1135 Impact factor: 3.293