Division of Swine Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150001, China.
Vet Microbiol. 2012 Oct 12;159(3-4):273-81. doi: 10.1016/j.vetmic.2012.06.018. Epub 2012 Jun 25.
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.
2006 年,高致病性猪繁殖与呼吸综合征病毒(HP-PRRSV)在中国出现,给养猪业造成了巨大的经济损失,至今仍是该行业的一大威胁。GP5 的 B 抗原决定区(AR)((37)SHL/FQLIYNL(45))被认为是 PRRSV 经典株的主要线性中和 AR。然而,最近的一项研究报告表明,针对该 AR 的肽纯化抗体不能中和 PRRSV。与经典 PRRSV 相比,HP-PRRSV 的 B AR 发生了一个氨基酸突变(L/F(39)→I(39))。为了研究 HP-PRRSV 的 B AR 在体外和体内诱导中和抗体(NA)的能力,制备了针对 B AR 的兔抗血清(突变和未突变)以及针对 HP-PRRSV 具有高 NA 滴度的猪高免血清。免疫荧光试验(IFA)表明,两种兔抗血清均对经典 PRRSV CH-1a 和 HP-PRRSV HuN4 具有反应性,IFA 滴度无明显差异。然而,抗血清对经典 PRRSV CH-1a 和 HP-PRRSV HuN4 没有中和活性。间接 ELISA 和病毒中和试验分别检测猪高免血清中的抗 B AR 肽抗体和 NA 水平之间没有相关性。B AR 肽特异性血清抗体没有中和活性,GST-B 融合蛋白不能抑制猪高免血清中 NA 的中和作用。基于这些发现,我们得出结论,HP-PRRSV 的 B AR 不是 HP-PRRSV GP5 的中和 AR。