Wu Zhuan-Chang, Zhu Mei-Zhen, Bian Xiao-Ming, Ma Cheng-Tai, Zhao Peng, Cui Zhi-Zhong
College of Animal Science and Technology, Shandong Agricultural University, Shandong Engineering Research Center for Animal Disease Control and Prevention, Taian 271018, China.
Bing Du Xue Bao. 2011 Sep;27(5):447-55.
The purpose of this study was to compare the whole genome sequences and replication dynamics in cell cultures of two Avian leukosis viruses of subgroup B (ALV) isolates, SDAU09E3 and SDAU09C2. Comparison of the amino acid sequences indicated that the gp85 identity of these two subgroup B isolates was 95.4%, the identity with other three ALV-B reference strains was 91.0%-94.9%, and less than 87.9% with ALV subgroup A, C, D, E and J. Comparison of the nucleotide sequence of gag and pol genes indicated that homologies of gag gene and pol gene of these two ALV-B isolates with all compared reference strains of different subgroups were above 93%. Homologies of LTR sequence of these two ALV-B isolates with other exogenous ALVs subgroups A, B, C, D and J were 72.6%-88.3%, but only 51.5% when compared with endogenous ALV subgroup E. The identity of LTR between these two ALV-B strains was only 74.8%, which was far lower than the identity of other genes. The identity of U3 region of LTR between these two ALV-B isolates was only 68.8% and there were obvious differences in the number CAAT Boxes. Replication dynamics in DF-1 cell indicated that the value of TCID50 was similar between 2 isolates but the concentration of nucleocapsid protein p27 antigen of SDAU09E3 was significantly higher than SDAU09C2 in cell culture supernatant, which indicated there was no parallel relationship between p27 antigen concentration and infectious virus particles. Whether such difference was resulted from the diversity of U3 region of LTR, further studies with their recombinant infectious clones is necessary.
本研究的目的是比较两个B亚群禽白血病病毒(ALV)分离株SDAU09E3和SDAU09C2在细胞培养物中的全基因组序列和复制动力学。氨基酸序列比较表明,这两个B亚群分离株的gp85同一性为95.4%,与其他三个ALV-B参考毒株的同一性为91.0%-94.9%,与A、C、D、E和J亚群ALV的同一性低于87.9%。gag和pol基因的核苷酸序列比较表明,这两个ALV-B分离株的gag基因和pol基因与所有比较的不同亚群参考毒株的同源性均高于93%。这两个ALV-B分离株的LTR序列与其他外源性ALV亚群A、B、C、D和J的同源性为72.6%-88.3%,但与内源性ALV亚群E相比仅为51.5%。这两个ALV-B毒株之间LTR的同一性仅为74.8%,远低于其他基因的同一性。这两个ALV-B分离株之间LTR的U3区域同一性仅为68.8%,且CAAT框数量存在明显差异。DF-1细胞中的复制动力学表明,两个分离株之间的TCID50值相似,但细胞培养上清液中SDAU09E3的核衣壳蛋白p27抗原浓度显著高于SDAU09C2,这表明p27抗原浓度与感染性病毒颗粒之间不存在平行关系。这种差异是否由LTR的U3区域多样性导致,有必要对其重组感染性克隆进行进一步研究。