NDV was considered as the important avian virus causing great damage in poultry industry. NDV selectively replicates in chicken and tumor cells, but not in normal cells. The study of NDV replication mechanism is of great significance to anti-NDV and anti-tumor therapy. Mammalian cells enter a relatively stable state by temporarily inhibiting cellular protein translation when exposed to various environmental stressors. In this case, SG is induced to arrest cytoplasmic mRNA, protein translation factors, and RNA binding proteins. In our current study, NDV triggered stable formation of bona fide SG through PKR/eIF2a pathway. NDV infection results in the inhibition of total host protein translation but not viral protein translation. SG blockage significantly inhibits virus replication. Mechanistically, SG specifically recruits host mRNA, whereas virus mRNA employs some unknown mechanism to escape from SG package. Blockage of SG results in the release of host mRNA into polysomes to competitively binds to translation factors, which lead to the decrease of viral mRNA translation level. This results give an explanation how virus utilize SG to promote its own replication.

Most of the previous reports identified SG as a host defense mechanism. Few of reports showed the pro-viral role of SG. However, the concrete mechanism has not been elucidated. Our study first give the explanation of how SG promotes virus infection, which is of great theoretical value and practical significance.

The first author of the study is Dr. Yingjie Sun from Shanghai Veterinary Research Institute. The corresponding author is Prof. Chan Ding, the chief expert of Waterfowl Virus Innovation Team. The study was supported by the National Natural Science Foundation and The Innovation Project Funding of Chinese Academy of Agricultural Science.

Paper link：http://www.fasebj.org/content/early/2016/12/23/fj.201600980R.abstract


 

By Sun Yingjie     
 sunyingjie@shvri.ac.cn