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.

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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

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article

Avian deltacoronaviruses encode fusion-associated small transmembrane proteins that can induce syncytia formation

Kylie Sartalamacchia, Vanesa Veletanlic, Monique S. Porter, Kristen M. Ogden
2 citations
Virology
Animal Virus Infections Studies
0.68
article

Avian deltacoronaviruses encode fusion-associated small transmembrane proteins that can induce syncytia formation

Kylie Sartalamacchia, Vanesa Veletanlic, Monique S. Porter, Kristen M. Ogden
article en
2 citations

Abstract

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.

VirologyVol. 600
Vanderbilt University Medical Center (US)
Vanderbilt University, National Institutes of Health
Openalex Percentile: Top 32%
Animal Virus Infections Studies
0.68
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Avian deltacoronaviruses encode fusion-associated small transmembrane proteins that can induce syncytia formation — Kylie Sartalamacchia, Vanesa Veletanlic, et al. · Virology (2024) | TGRS Research Map | TGRS