Publication: Interaction between Kazal serine proteinase inhibitor SPIPm2 and viral protein WSV477 reduces the replication of white spot syndrome virus
Issued Date
2013-09-01
Resource Type
ISSN
10959947
10504648
10504648
Other identifier(s)
2-s2.0-84882897048
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Fish and Shellfish Immunology. Vol.35, No.3 (2013), 957-964
Suggested Citation
Sirikwan Ponprateep, Kornsunee Phiwsaiya, Anchalee Tassanakajon, Vichien Rimphanitchayakit Interaction between Kazal serine proteinase inhibitor SPIPm2 and viral protein WSV477 reduces the replication of white spot syndrome virus. Fish and Shellfish Immunology. Vol.35, No.3 (2013), 957-964. doi:10.1016/j.fsi.2013.07.009 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/30983
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
Interaction between Kazal serine proteinase inhibitor SPIPm2 and viral protein WSV477 reduces the replication of white spot syndrome virus
Abstract
White spot syndrome (WSS) is a viral disease caused by white spot syndrome virus (WSSV) which leads to severe mortality in cultured penaeid shrimp. In response to WSSV infection in Penaeus monodon, a Kazal serine proteinase inhibitor SPI. Pm2, normally stored in the granules of granular and semi-granular hemocytes is up-regulated and found to deter the viral replication. By using yeast two-hybrid screening, we have identified a viral target protein, namely WSV477. Instead of being a proteinase, the WSV477 was reported to be a Cys2/Cys2-type zinc finger regulatory protein having ATP/GTP-binding activity. Invitro pull down assay confirmed the protein-protein interaction between rSPI. Pm2 and rWSV477. Confocal laser scanning microscopy demonstrated that the SPI. Pm2 and WSV477 were co-localized in the cytoplasm of shrimp hemocytes. Using RNA interference, the silencing of WSV477 resulted in down-regulated of viral late gene VP28, the same result obtained with SPI. Pm2. In this instance, the SPI. Pm2 does not function as proteinase inhibitor but inhibit the regulatory function of WSV477. © 2013 Elsevier Ltd.