An avian leukosis virus subgroup J isolate with a Rous sarcoma virus-like 59-LTR shows enhanced replication capability

نویسندگان

  • Yanni Gao
  • Xiaolu Guan
  • Yongzhen Liu
  • Xiaofei Li
  • Bingling Yun
  • Xiaole Qi
  • Yongqiang Wang
  • Honglei Gao
  • Hongyu Cui
  • Changjun Liu
  • Yanping Zhang
  • Xiaomei Wang
  • Yulong Gao
چکیده

Avian leukosis virus subgroup J (ALV-J) was first isolated from meat-producing chickens that had developed myeloid leukosis. However, ALV-J infections associated with hemangiomas have occurred in egg-producing (layer) flocks in China. In this study, we identified an ALV-J layer isolate (HLJ13SH01) as a recombinant of ALV-J and a Rous sarcoma virus Schmidt-Ruppin B strain (RSV-SRB), which contained the RSV-SRB 59-LTR and the other genes of ALV-J. Replication kinetic testing indicated that the HLJ13SH01 strain replicated faster than other ALV-J layer isolates in vitro. Sequence analysis indicated that the main difference between the two isolates was the 59-LTR sequences, particularly the U3 sequences. A 19 nt insertion was uniquely found in the U3 region of the HLJ13SH01 strain. The results of a Dual-Glo luciferase assay revealed that the 19 nt insertion in the HLJ13SH01 strain increased the enhancer activity of the U3 region. Moreover, an additional CCAAT/enhancer element was found in the 19 nt insertion and the luciferase assay indicated that this element played a key role in increasing the enhancer activity of the 59-U3 region. To confirm the potentiation effect of the 19 nt insertion and the CCAAT/ enhancer element on virus replication, three infectious clones with 59-U3 region variations were constructed and rescued. Replication kinetic testing of the rescued viruses demonstrated that the CCAAT/enhancer element in the 19 nt insertion enhanced the replication capacity of the ALV-J recombinant in vitro.

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تاریخ انتشار 2014