Yoo Dongwan, Welch Siao-Kun W, Lee Changhee, Calvert Jay G
Department of Pathobiology, Ontario Veterinary College, University of Guelph, Guelph, Ont., N1G 2W1, Canada.
Vet Immunol Immunopathol. 2004 Dec 8;102(3):143-54. doi: 10.1016/j.vetimm.2004.09.019.
Full-length infectious cDNA clones have recently become available for both European and North American genotypes of porcine reproductive and respiratory syndrome virus (PRRSV), and it is now possible to alter the PRRSV genome and create genetically defined mutant viruses. Among many possible applications of the PRRSV infectious cDNA clones, development of genetically modified vaccines is of particular interest. Using infectious clones, the PRRSV genome has been manipulated by changing individual amino acids, deleting coding regions, inserting foreign sequences, and generating arterivirus chimeras. The limited available data suggest that all structural proteins of PRRSV are essential for replication of the virus, and that PRRSV infectivity is relatively intolerant of subtle changes within the structural proteins. The major tasks in PRRSV research are to identify virulence factors and pathogenic mechanisms, and to understand the structure-function relationships of individual viral proteins. Utilizing these infectious clones as tools, a new generation of safe and efficacious PRRS vaccines may be constructed.
最近,欧洲型和北美型猪繁殖与呼吸综合征病毒(PRRSV)的全长感染性cDNA克隆均已获得,现在有可能改变PRRSV基因组并创建基因明确的突变病毒。在PRRSV感染性cDNA克隆的众多可能应用中,转基因疫苗的开发尤其令人关注。利用感染性克隆,通过改变单个氨基酸、删除编码区、插入外源序列以及构建动脉炎病毒嵌合体等方式对PRRSV基因组进行了操作。有限的现有数据表明,PRRSV的所有结构蛋白对于病毒复制都是必不可少的,并且PRRSV的感染性相对不耐受结构蛋白内的细微变化。PRRSV研究的主要任务是鉴定毒力因子和致病机制,以及了解单个病毒蛋白的结构-功能关系。利用这些感染性克隆作为工具,可能构建出新一代安全有效的PRRS疫苗。