Han Jun, Wang Yue, Faaberg Kay S
Department of Veterinary and Biomedical Sciences, 205 Veterinary Science Building, 1971 Commonwealth Avenue, University of Minnesota, Saint Paul, MN 55108, USA.
Virus Res. 2006 Dec;122(1-2):175-82. doi: 10.1016/j.virusres.2006.06.003. Epub 2006 Jul 21.
Two full-length genomes of recently emerged virulent isolates of porcine reproductive and respiratory syndrome virus (PRRSV) were sequenced and compared to other PRRSV strains. The results revealed that these two isolates (named MN184), of North American lineage, represented the shortest PRRSV genomes sequenced to date with a nucleotide length of 15019 bases. Genetic analysis demonstrated that the two isolates were not identical and shared approximately 87 and 59% nucleotide identity with prototype North American strain VR-2332 and European strain Lelystad, respectively. Three quite variable regions were identified, corresponding to putative nsp1beta, putative nsp2 and ORF5. Nsp2, the most variable region, shared only 66-70% amino acid similarity to other sequenced North American-like PRRSV nsp2 proteins. Further study revealed that the nsp2 protein of the MN184 isolates contained three discontinuous deletions when compared to strain VR-2332 nsp2 protein, with the sizes of 111, 1, and 19 amino acids corresponding to strain VR-2332 positions 324-434, 486 and 505-523, respectively. The results suggest that targeted manipulation of PRRSV through nsp2 modification by reverse genetics may yield promising vectors for vaccine development, as has been recently demonstrated [Han, J., Faaberg, K.S., Wang, Y., Liu, H., 2005. Non-structural protein 2 mutants of PRRSV strain VR-2332 infectious clone based on deletions seen in RFLP184 isolates are viable. In: PRRS International Symposium Proceedings, vol. 8, Saint Louis, MO].
对最近出现的猪繁殖与呼吸综合征病毒(PRRSV)强毒株的两个全长基因组进行了测序,并与其他PRRSV毒株进行了比较。结果显示,这两个北美谱系的毒株(命名为MN184)代表了迄今为止测序的最短PRRSV基因组,核苷酸长度为15019个碱基。遗传分析表明,这两个毒株并不相同,与北美原型毒株VR - 2332和欧洲毒株莱利斯塔德的核苷酸同一性分别约为87%和59%。鉴定出三个变异较大的区域,分别对应假定的nsp1β、假定的nsp2和开放阅读框5。nsp2是变异最大的区域,与其他已测序的北美型PRRSV nsp2蛋白的氨基酸相似性仅为66 - 70%。进一步研究发现,与VR - 2332毒株的nsp2蛋白相比,MN184毒株的nsp2蛋白包含三个不连续的缺失,大小分别为111、1和19个氨基酸,分别对应VR - 2332毒株的第324 - 434、486和505 - 523位。结果表明,通过反向遗传学对nsp2进行修饰来靶向操纵PRRSV,可能会产生用于疫苗开发的有前景的载体,正如最近所证明的那样[Han, J., Faaberg, K.S., Wang, Y., Liu, H., 2005.基于RFLP184分离株中观察到的缺失构建的PRRSV毒株VR - 2332感染性克隆的非结构蛋白2突变体是可行的。载于:《PRRS国际研讨会论文集》,第8卷,密苏里州圣路易斯] 。