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Zika Virus Hijacks Extracellular Vesicle Tetraspanin Pathways for Cell-to-Cell Transmission.

作者信息

York Sara B, Sun Li, Cone Allaura S, Duke Leanne C, Cheerathodi Mujeeb R, Meckes David G

机构信息

Florida State Universitygrid.255986.5 College of Medicine, Department of Biomedical Sciences, Tallahassee, Florida, USA.

出版信息

mSphere. 2021 Jun 30;6(3):e0019221. doi: 10.1128/mSphere.00192-21.


DOI:10.1128/mSphere.00192-21
PMID:34190582
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8265634/
Abstract

Extracellular vesicles (EVs) are membrane-encapsulated structures released by cells which carry signaling factors, proteins, and microRNAs that mediate intercellular communication. Accumulating evidence supports an important role of EVs in the progression of neurological conditions and both the spread and pathogenesis of infectious diseases. It has recently been demonstrated that EVs from hepatitis C virus (HCV)-infected individuals and cells contained replicative-competent viral RNA that was capable of infecting hepatocytes. Being a member of the same viral family, it is likely the Zika virus also hijacks EV pathways to package viral components and secrete vesicles that are infectious and potentially less immunogenic. As EVs have been shown to cross blood-brain and placental barriers, it is possible that Zika virus could usurp normal EV biology to gain access to the brain or developing fetus. Here, we demonstrate that Zika virus-infected cells secrete distinct EV subpopulations with specific viral protein profiles and infectious genomes. Zika virus infection resulted in the enhanced production of EVs with various sizes and densities compared to those released from noninfected cells. We also show that the EV-enriched tetraspanin CD63 regulates the release of EVs and Zika viral genomes and capsids following infection. Overall, these findings provide evidence for an alternative means of Zika virus transmission and demonstrate the role of EV biogenesis and trafficking proteins in the modulation of Zika virus infection and virion morphogenesis. Zika virus is a reemerging infectious disease that spread rapidly across the Caribbean and South America. Infection of pregnant women during the first trimester has been linked to microcephaly, a neurological condition where babies are born with smaller heads due to abnormal brain development. Babies born with microcephaly can develop convulsions and suffer disabilities as they age. Despite the significance of Zika virus, little is known about how the virus infects the fetus or causes disease. Extracellular vesicles (EVs) are membrane-encapsulated structures released by cells that are present in all biological fluids. EVs carry signaling factors, proteins, and microRNAs that mediate intercellular communication. EVs have been shown to be a means by which some viruses can alter cellular environments and cross previously unpassable cellular barriers. Thus, gaining a greater understanding of how Zika virus affects EV cargo may aid in the development of better diagnostics, targeted therapeutics, and/or prophylactic treatments.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/fc9a814e3bbb/msphere.00192-21-f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/ef9632b96ee4/msphere.00192-21-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/9c253d5c3b63/msphere.00192-21-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/1daba12e8961/msphere.00192-21-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/2457c1349082/msphere.00192-21-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/da8cc659c4b6/msphere.00192-21-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/fc9a814e3bbb/msphere.00192-21-f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/ef9632b96ee4/msphere.00192-21-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/9c253d5c3b63/msphere.00192-21-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/1daba12e8961/msphere.00192-21-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/2457c1349082/msphere.00192-21-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/da8cc659c4b6/msphere.00192-21-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/961b/8265634/fc9a814e3bbb/msphere.00192-21-f006.jpg

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引用本文的文献

[1]
Mosquito Exosomal Tetraspanin CD151 Facilitates Flaviviral Transmission and Interacts with ZIKV and DENV2 Viral Proteins.

Int J Mol Sci. 2025-7-31

[2]
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[3]
"Silent messengers of chaos: unveiling the dual threat of immune infiltrates in Japanese encephalitis virus neuroinflammatory storm".

Virol J. 2025-5-31

[4]
Extracellular vesicles in arbovirus infections: from basic biology to potential clinical applications.

Front Cell Infect Microbiol. 2025-4-28

[5]
Distinctive function of Tetraspanins: Implication in viral infections.

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[6]
Extracellular Vesicles as Biomarkers in Infectious Diseases.

Biology (Basel). 2025-2-11

[7]
Tetraspanin CD9 alters cellular trafficking and endocytosis of tetraspanin CD63, affecting CD63 packaging into small extracellular vesicles.

J Biol Chem. 2025-3

[8]
Extracellular vesicles in ZIKV infection: Carriers and facilitators of viral pathogenesis?

Sci Prog. 2025

[9]
An Overview of Zika Virus and Zika Virus Induced Neuropathies.

Int J Mol Sci. 2024-12-24

[10]
Extracellular vesicles promote the infection and pathogenicity of Japanese encephalitis virus.

J Extracell Vesicles. 2025-1

本文引用的文献

[1]
JC Polyomavirus Uses Extracellular Vesicles To Infect Target Cells.

mBio. 2019-4-9

[2]
Exosomes mediate Zika virus transmission through SMPD3 neutral Sphingomyelinase in cortical neurons.

Emerg Microbes Infect. 2019

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J Vis Exp. 2019-2-7

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PLoS Pathog. 2019-2-19

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Dengue virus requires apoptosis linked gene-2-interacting protein X (ALIX) for viral propagation.

Virus Res. 2018-12-29

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J Virol. 2019-3-5

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Vesicle-Cloaked Virus Clusters Are Optimal Units for Inter-organismal Viral Transmission.

Cell Host Microbe. 2018-8-8

[9]
Hepatitis C virus enters liver cells using the CD81 receptor complex proteins calpain-5 and CBLB.

PLoS Pathog. 2018-7-19

[10]
Arthropod EVs mediate dengue virus transmission through interaction with a tetraspanin domain containing glycoprotein Tsp29Fb.

Proc Natl Acad Sci U S A. 2018-6-26

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