Cell–cell transmission allows human T-lymphotropic virus 1 to circumvent tetherin restriction
Open accessAbstract
Tetherin is part of the cellular innate immunity and impedes cell-free transmission of viruses that bud from the plasma membrane by retaining them on the cell surface. Some viruses have evolved activities in different proteins such as Vpu (HIV-1), K-protein (KSHV), Nef (SIV) or Env (HIV-2) to downregulate tetherin and overcome its restriction. We found that chronically HTLV-1 infected T-cell lines express eightfold more tetherin than uninfected transformed T-cell lines suggesting that tetherin expression is not inhibited by the virus. We observed that even small amounts of exogenous tetherin caused the retention of HTLV-1 on the cell surface and severely reduced cell-free infectivity of HTLV-1, but that cell-cell transmission, which is more relevant for HTLV-1, was significantly less decreased. However, knock-down of tetherin expresssion resulted in a slight increase in cell-cell infection indicating that the protein does not enhance this route of transmission.
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HTLV-1 viral clusters are enriched with galectin-3 and tetherin.
“Additionally, the viral clusters were found to be enriched with galectin-3, which forms the ECM lattice, and tetherin, which retains budding viral particles on the cell surface [99].”
From HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread (2022) · cites this paper as [99]
Cites
Avoiding the void: Cell-to-cell spread of human viruses
Sattentau, Q. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1972 · Cited by 614 · see citing works
Derse, D., Hill, S. A., Lloyd, P. A., Chung, H.-K., & Morse, B. A. (2001) · Journal of Virology · doi:10.1128/jvi.75.18.8461-8468.2001 · Cited by 145 · see citing works
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HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread
Kalinichenko, S., Komkov, D., & Mazurov, D. (2022) · Viruses · doi:10.3390/v14010152 · Cited by 68 · see citing works
“Additionally, the viral clusters were found to be enriched with galectin-3, which forms the ECM lattice, and tetherin, which retains budding viral particles on the cell surface [99].”
Background
- Authors
- Ilinskaya, A., Derse, D., Hill, S., Princler, G., & Heidecker, G.
- Affiliations
- Frederick National Laboratory for Cancer Research (US)
- Corresponding author
- Heidecker, Gisela
- Venue
- Virology
- Publisher
- Elsevier BV
- Published
- 2013-02
- Volume
- 436
- Issue
- 1
- Pages
- 201-209
- ISSN
- 0042-6822 (ISSN-L)
- OpenAlex
- W2067380134
- Cited by
- 30
- References
- 2
- Citations by year
- 2025: 1 · 2023: 1 · 2022: 4 · 2021: 1 · 2020: 2 · 2019: 2 · 2018: 2 · 2017: 8 · 2016: 1 · 2015: 1 · 2014: 2 · 2013: 5
- FWCI
- 1.11
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Virology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health, National Cancer Institute, Center for Cancer Research
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and Retrovirus Studies
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
- Keywords
- HTLV-1, tetherin, cell-to-cell transmission, innate immunity, T cell lines, chronic infection, viral infectivity
- MeSH terms
- Bone Marrow Stromal Antigen 2, Cell Communication, Cell Line, Cell Line, Transformed, Humans, Immunity, Innate, T-Lymphocytes, Human T-lymphotropic virus 1, CD4-Positive T-Lymphocytes, Antigens, CD, RNA Interference, RNA, Small Interfering, Virus Release, GPI-Linked Proteins
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