Mary Wilson
Well-known member
15 July 2024
DOI: https://doi.org/10.1128/jvi.00775-24
Authors: Judith M. Reyes Ballista, Ashley J. Hoover, Joseph T. Noble, Marissa D. Acciani, Kerri L. Miazgowicz, Sarah A. Harrison, Grace Andrea L. Tabscott, Avery Duncan, Don N.Barnes, Ariana R. Jimenez, Melinda A. Brindley
ABSTRACT
T-cell immunoglobin and mucin domain protein-1 (TIM-1) mediates entry of chikungunya virus (CHIKV) into some mammalian cells through the interaction with envelope phospholipids. While this interaction enhances entry, TIM-1 has been shown to tether newly formed HIV and Ebola virus particles, limiting their efficient release. In this study, we investigate the ability of surface receptors such as TIM-1 to sequester newly budded virions on the surface of infected cells. We established a luminescence reporter system to produce chikungunya viral particles that integrate nano-luciferase and easily quantify viral particles. We found that TIM-1 on the surface of host cells significantly reduced CHIKV release efficiency in comparison to other entry factors. Removal of cell surface TIM-1 through direct cellular knock-out or altering the cellular lipid distribution enhanced CHIKV release. Over the course of infection, CHIKV was able to counteract the tethering effect by gradually decreasing the surface levels of TIM-1 in a process mediated by the nonstructural protein 2. This study highlights the importance of phosphatidylserine receptors in mediating not only the entry of CHIKV but also its release and could aid in developing cell lines capable of enhanced vaccine production.
https://journals.asm.org/doi/abs/10.1128/jvi.00775-24
DOI: https://doi.org/10.1128/jvi.00775-24
Authors: Judith M. Reyes Ballista, Ashley J. Hoover, Joseph T. Noble, Marissa D. Acciani, Kerri L. Miazgowicz, Sarah A. Harrison, Grace Andrea L. Tabscott, Avery Duncan, Don N.Barnes, Ariana R. Jimenez, Melinda A. Brindley
ABSTRACT
T-cell immunoglobin and mucin domain protein-1 (TIM-1) mediates entry of chikungunya virus (CHIKV) into some mammalian cells through the interaction with envelope phospholipids. While this interaction enhances entry, TIM-1 has been shown to tether newly formed HIV and Ebola virus particles, limiting their efficient release. In this study, we investigate the ability of surface receptors such as TIM-1 to sequester newly budded virions on the surface of infected cells. We established a luminescence reporter system to produce chikungunya viral particles that integrate nano-luciferase and easily quantify viral particles. We found that TIM-1 on the surface of host cells significantly reduced CHIKV release efficiency in comparison to other entry factors. Removal of cell surface TIM-1 through direct cellular knock-out or altering the cellular lipid distribution enhanced CHIKV release. Over the course of infection, CHIKV was able to counteract the tethering effect by gradually decreasing the surface levels of TIM-1 in a process mediated by the nonstructural protein 2. This study highlights the importance of phosphatidylserine receptors in mediating not only the entry of CHIKV but also its release and could aid in developing cell lines capable of enhanced vaccine production.
https://journals.asm.org/doi/abs/10.1128/jvi.00775-24