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Human T-lymphotropic virus-1 visualized at the virological synapse by electron tomography
Endre Majorovits1, Mohamed Nejmeddine, Yuetsu Tanaka
1Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Insights
Human T-lymphotropic virus 1 (HTLV-1) directly transmits via a virological synapse (VS). This study reveals enveloped HTLV-1 particles within the VS, confirming cell-to-cell viral transfer.
Area of Science:
- Virology
- Cell Biology
- Immunology
Background:
- Human T-lymphotropic virus 1 (HTLV-1) transmission occurs via cell-cell contact (virological synapse, VS).
- The ultrastructure of the HTLV-1 VS and the nature of transmitted viral particles were previously unknown.
- Cell-free HTLV-1 virions are undetectable, yet viral envelope protein is crucial for infectivity, suggesting direct particle transfer.
Purpose of the Study:
- To elucidate the ultrastructure of the HTLV-1 virological synapse.
- To determine the nature of HTLV-1 particles transmitted during cell-cell contact.
- To visualize the direct cell-to-cell transmission mechanism of HTLV-1.
Main Methods:
- Utilized electron tomography combined with immunostaining for viral proteins.
- Analyzed virological synapses formed between naturally HTLV-1 infected lymphocytes.
- Reconstructed 3D images to visualize viral particle location and interaction within the VS.
Main Results:
- Demonstrated the presence of enveloped HTLV-1 particles within the virological synapse.
- Showed HTLV-1 particles within multiple synaptic clefts simultaneously in 3D.
- Observed HTLV-1 virions contacting the recipient cell membrane before detachment.
Conclusions:
- The HTLV-1 virological synapse facilitates direct cell-to-cell transmission of enveloped viral particles.
- Transmission involves triggered, directional release of HTLV-1 into confined intercellular spaces.
- This mechanism explains the infectivity of HTLV-1 despite the absence of cell-free virions.
Abstract:
Human T-lymphotropic virus 1 (HTLV-1) is transmitted directly between cells via an organized cell-cell contact called a virological synapse (VS). The VS has been studied by light microscopy, but the ultrastructure of the VS and the nature of the transmitted viral particle have remained unknown. Cell-free enveloped virions of HTLV-1 are undetectable in the serum of individuals infected with the human T-lymphotropic virus 1 (HTLV-1) and during in vitro culture of naturally infected lymphocytes. However, the viral envelope protein is required for infectivity of HTLV-1, suggesting that complete, enveloped HTLV-1 virions are transferred across the synapse. Here, we use electron tomography combined with immunostaining of viral protein to demonstrate the presence of enveloped HTLV-1 particles within the VS formed between naturally infected lymphocytes. We show in 3D that HTLV-1 particles can be detected in multiple synaptic clefts at different locations simultaneously within the same VS. The synaptic clefts are surrounded by the tightly apposed plasma membranes of the two cells. HTLV-1 virions can contact the recipient cell membrane before detaching from the infected cell. The results show that the HTLV-1 virological synapse that forms spontaneously between lymphocytes of HTLV-1 infected individuals allows direct cell-cell transmission of the virus by triggered, directional release of enveloped HTLV-1 particles into confined intercellular spaces.
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