Viral circular RNA-encoded protein, ceVP28, divulges an antiviral response in invertebrates
Issued Date
2025-02-25
Resource Type
eISSN
10916490
Scopus ID
2-s2.0-85218932441
Pubmed ID
39964719
Journal Title
Proceedings of the National Academy of Sciences of the United States of America
Volume
122
Issue
8
Rights Holder(s)
SCOPUS
Bibliographic Citation
Proceedings of the National Academy of Sciences of the United States of America Vol.122 No.8 (2025)
Suggested Citation
Limkul S., Phiwthong T., Wanvimonsuk S., Seabkongseng T., Aunkam P., Jaree P., Luangtrakul W., Mahanil K., Teamtisong K., Tittabutr P., Teaumroong N., Sarnow P., Wang H.C., Somboonwiwat K., Boonchuen P. Viral circular RNA-encoded protein, ceVP28, divulges an antiviral response in invertebrates. Proceedings of the National Academy of Sciences of the United States of America Vol.122 No.8 (2025). doi:10.1073/pnas.2321707122 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/105576
Title
Viral circular RNA-encoded protein, ceVP28, divulges an antiviral response in invertebrates
Corresponding Author(s)
Other Contributor(s)
Abstract
Invertebrates mostly use innate immunity to counteract pathogenic infections. In this study, shrimp was used as a model organism to explore the functions of circular RNAs (circRNAs) derived from white spot syndrome virus (WSSV). We identified four viral circRNAs, termed circWSSV147, circWSSV326, circWSSV458, and circVP28, from transcriptomic data of WSSV-infected shrimp. CircVP28, which contains an internal ribosome entry site, was further characterized to determine its potential as a template for protein translation. We observed the presence of a truncated, circRNA-encoded VP28 (ceVP28) in infected shrimp. Both ceVP28 and its parental counterpart, VP28, share the same host cell binding partner Rab7, which is a host receptor for WSSV. Coadministration of recombinant ceVP28 protein and WSSV to penaeid shrimps reduced both viral copy numbers and mortality upon WSSV challenges. These findings uncovered a host defense mechanism by which a protein encoded by a viral circRNA modulates virus-receptor interactions, resulting in blocking of viral entry.