Plagemann Peter G W
Department of Microbiology, University of Minnesota, MMC 196, Minneapolis, MN 55455, USA.
Vet Immunol Immunopathol. 2004 Dec 8;102(3):263-75. doi: 10.1016/j.vetimm.2004.09.011.
I have used indirect ELISA with overlapping synthetic peptides representing the GP5 ectodomain to study the generation and specificity of peptide-binding Abs in pigs that were infected in utero with porcine reproductive and respiratory syndrome virus (PRRSV) strain VR2332 and in North American field sera submitted for PRRSV infection diagnosis. Peptide-binding Abs appeared in sera of the VR2332-infected pigs within about 30 days post-farrowing (dpf), reaching maximum titers 100-200 dpf and then decreasing slowly to about half of maximum titer by about 400 dpf. The formation of peptide-binding Abs and of virus neutralizing Abs correlated and their initial appearance coincided with disappearance of virus from the circulation. The Abs were specific for VR2332-specific peptides. In contrast, anti-N-protein Abs as measured by HerdCheck ELISA appeared within 7 dpf, reached maximum levels at about 100 dpf and had decreased below detectable levels by about 200 dpf. Twenty-seven field serum samples with virus neutralizing activity all possessed high levels of peptide binding Abs, but the Abs bound about equally to VR2332 and strain Lelystad virus (LV)-specific peptides. The indirect ELISA results using various large peptides and competition ELISA using small peptides (8 or 9 amino acids long) confirmed that the epitope recognized by the Abs is located in the GP5 ectodomain sequence 37SHLQLIYNL of VR2332. Use of mutated peptides in the competition ELISA showed that 42I to T and 38HL to TY substitutions blocked Ab recognition, whereas deletion of 41L had no effect. In addition, 26 serum samples submitted by two farms for diagnostic tests were found to possess low levels of Abs that bound to GP5 ectodomain peptides, even though the sera were sero-negative in the HerdChek ELISA and lacked neutralizing activity. Competition ELISA showed that the Abs recognized one or more epitopes located downstream of the PRRSV neutralization epitope. An epitope(s) located in the same area was recognized by Abs generated in mice by immunization with a GP5 ectodomain peptide conjugated to BSA. These Abs also lacked neutralizing activity.
我使用间接ELISA法,利用代表GP5胞外域的重叠合成肽,研究了子宫内感染猪繁殖与呼吸综合征病毒(PRRSV)VR2332株的仔猪以及提交用于PRRSV感染诊断的北美田间血清中肽结合抗体的产生和特异性。肽结合抗体在分娩后约30天(dpf)出现在VR2332感染仔猪的血清中,在100 - 200 dpf达到最高滴度,然后缓慢下降,到约400 dpf时降至最高滴度的一半左右。肽结合抗体和病毒中和抗体的形成相关,它们的最初出现与病毒从循环中的消失同时发生。这些抗体对VR2332特异性肽具有特异性。相比之下,通过HerdCheck ELISA检测的抗N蛋白抗体在7 dpf内出现,在约100 dpf达到最高水平,到约200 dpf时已降至可检测水平以下。27份具有病毒中和活性的田间血清样本均具有高水平的肽结合抗体,但这些抗体与VR2332和莱利斯塔德病毒(LV)特异性肽的结合程度大致相同。使用各种大肽的间接ELISA结果以及使用小肽(8或9个氨基酸长)的竞争ELISA结果证实,抗体识别的表位位于VR2332的GP5胞外域序列37SHLQLIYNL中。在竞争ELISA中使用突变肽表明,42I突变为T以及38HL突变为TY会阻断抗体识别,而缺失41L则没有影响。此外,发现两个农场提交用于诊断测试的26份血清样本中,与GP5胞外域肽结合的抗体水平较低,尽管这些血清在HerdChek ELISA中呈血清阴性且缺乏中和活性。竞争ELISA表明,这些抗体识别位于PRRSV中和表位下游的一个或多个表位。通过用与牛血清白蛋白(BSA)偶联的GP5胞外域肽免疫小鼠产生的抗体识别位于同一区域的一个表位。这些抗体也缺乏中和活性。