Rodriguez M J, Sarraseca J, Garcia J, Sanz A, Plana-Durán J, Ignacio Casal J
INGENASA, Madrid, Spain.
J Gen Virol. 1997 Sep;78 ( Pt 9):2269-78. doi: 10.1099/0022-1317-78-9-2269.
Two major genotypes of porcine reproductive and respiratory syndrome virus (PRRSV) have been described, which correspond to the European and North American isolates. PRRSV nucleocapsid (N) protein has been identified as the most immunodominant viral protein. The N genes from two PRRSV isolates, Olot/91 (European) and Québec 807/94 (North American), were cloned and expressed in: (i) baculovirus under the control of the polyhedrin promoter and (ii) Escherichia coli using the pET3x system. The N protein from both isolates was expressed much more efficiently in E. coli as a fusion protein than in baculovirus. The antigenicity of the protein was similar in both systems and it was recognized by a collection of 48 PRRSV-positive pig sera. The antigenic structure of the PRRSV N protein was investigated using seven monoclonal antibodies (MAbs) and overlapping fragments of the protein expressed in E. coli. Four MAbs recognized two discontinuous epitopes that were present in the partially folded protein, or at least a large fragment comprising the first 78 residues. The other three MAbs revealed the presence of a common antigenic site localized in the central region of the protein (amino acids 50-66). This region is well conserved among different isolates of European and North American origin and is the most hydrophilic region of the protein. However, this epitope, although recognized by the MAbs and many pig sera, is not useful for diagnostic purposes. Moreover, none of the N protein fragments were able to mimic the antigenicity of the entire protein.
已描述了猪繁殖与呼吸综合征病毒(PRRSV)的两种主要基因型,它们分别对应于欧洲和北美分离株。PRRSV核衣壳(N)蛋白已被确定为免疫显性最强的病毒蛋白。来自两种PRRSV分离株Olot/91(欧洲株)和魁北克807/94(北美株)的N基因被克隆并在以下系统中表达:(i)在多角体蛋白启动子控制下的杆状病毒中;(ii)使用pET3x系统在大肠杆菌中。两种分离株的N蛋白作为融合蛋白在大肠杆菌中表达的效率比在杆状病毒中高得多。该蛋白在两个系统中的抗原性相似,并且能被48份PRRSV阳性猪血清识别。使用七种单克隆抗体(MAb)和在大肠杆菌中表达的该蛋白的重叠片段研究了PRRSV N蛋白的抗原结构。四种MAb识别出存在于部分折叠蛋白中或至少包含前78个残基的大片段中的两个不连续表位。另外三种MAb揭示了位于该蛋白中心区域(氨基酸残基50 - 66)的一个共同抗原位点的存在。该区域在欧洲和北美来源的不同分离株中高度保守,并且是该蛋白最亲水的区域。然而,尽管该表位能被MAb和许多猪血清识别,但它对诊断用途并无帮助。此外,没有一个N蛋白片段能够模拟整个蛋白的抗原性。