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高致病性猪繁殖与呼吸综合征病毒 GP5 B 抗原区不是中和抗原区。

Highly pathogenic porcine reproductive and respiratory syndrome virus GP5 B antigenic region is not a neutralizing antigenic region.

机构信息

Division of Swine Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150001, China.

出版信息

Vet Microbiol. 2012 Oct 12;159(3-4):273-81. doi: 10.1016/j.vetmic.2012.06.018. Epub 2012 Jun 25.

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.

摘要

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。

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