Avian deltacoronaviruses encode fusion-associated small transmembrane proteins that can induce syncytia formation
Fusion-associated small transmembrane (FAST) proteins are nonstructural viral proteins that induce cell-cell fusion. FAST proteins, which previously were identified in the genomes of double-stranded RNA viruses, typically contain an acylated N-terminal ectodomain, central transmembrane domain, and C-terminal endodomain with a polybasic region. Using sequence homology and protein motif prediction, we identified accessory proteins in a subset of avian deltacoronaviruses as putative FAST proteins. Transient expression of thrush coronavirus NS7b or common moorhen coronavirus NS7a, but not night heron coronavirus NS7b, induced cell-cell fusion. Syncytia were detected in primate kidney epithelial cells or fibroblasts but not chicken embryo fibroblasts, and addition of an N-terminal FLAG peptide to the proteins ablated fusion activity. These findings suggest that multiple avian deltacoronaviruses, positive-sense RNA viruses, encode nonstructural proteins that can mediate cell-cell fusion and share features with known FAST proteins. Additional studies are needed to understand contributions of these proteins to deltacoronavirus biology.
Authors
- Kylie Sartalamacchia
- Vanesa Veletanlic
- Monique S. Porter
- Kristen M. Ogden (ORCID: https://orcid.org/0000-0002-2670-4335)
Institutions
- Vanderbilt University Medical Center (US)
Publication Details
- Journal
- Virology
- Published
- 2024-10-09
- DOI
- https://doi.org/10.1016/j.virol.2024.110258
- Citations
- 2
- Primary Topic
- Animal Virus Infections Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.68
Funders
- Vanderbilt University
- National Institutes of Health