The emerging novel avian leukosis virus with mutations in the pol gene shows competitive replication advantages both in vivo and in vitro

Emerg Microbes Infect. 2018 Jun 26;7(1):117. doi: 10.1038/s41426-018-0111-4.

Abstract

The avian leukosis virus subgroup K (ALV-K), a novel subgroup in Chinese indigenous chicken breeds, has been difficult to isolate in the past due to its poor replication ability. However, according to the latest monitoring data, the replication ability and isolation rate of ALV-K have clearly increased, and new strains with mutations in the pol gene have also been found. To determine the effects of such mutations on the biological characteristics of ALV-K, a pair of infectious clones were constructed and rescued. The first virus was an ALV-K Chinese isolate with mutations in its pol gene, named rSDAUAK-11. The second virus was a recuperative rSDAUAK-11 from which mutations in the pol gene were recovered according to the corresponding region of the ALV-K prototype virus JS11C1, named rRSDAUAK-11. In addition, two quantitative real-time polymerase chain reaction assays were developed to specifically detect these virus strains. Using such methods, we observed a marked improvement of the reverse transcriptase activity, replication ability and vertical transmission ability of rSDAUAK-11, which also revealed a formidable competitive advantage in mixed infection with rRSDAUAK-11 and corresponded to the differences between the wild strains SDAUAK-11 and JS11C1. Accordingly, our findings not only show that mutations in the pol gene are an important molecular mechanism contributing to corresponding changes in the biological characteristics of the newest ALV-K but also emphasize the potential future eradication of ALV.

MeSH terms

  • Animals
  • Avian Leukosis / transmission
  • Avian Leukosis / virology*
  • Avian Leukosis Virus / isolation & purification
  • Avian Leukosis Virus / physiology*
  • Chickens / virology*
  • DNA Mutational Analysis
  • Genes, pol*
  • Genome, Viral
  • Genomic Instability
  • Infectious Disease Transmission, Vertical
  • Mutation*
  • Virus Replication*