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Updated: Jul 5, 2025

Zika Virus Infectious Cell Culture System and the In Vitro Prophylactic Effect of Interferons
Published on: August 23, 2016
Zika Virus-Infected Monocyte Exosomes Mediate Cell-to-Cell Viral Transmission
Pedro Pablo Martínez-Rojas1, Verónica Monroy-Martínez1, Lourdes Teresa Agredano-Moreno2
1Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México 04510, México.
Abstract:
Zika fever is a reemerging arthropod-borne viral disease; however, Zika virus (ZIKV) can be transmitted by other, non-vector means. Severe Zika fever is characterized by neurological disorders, autoimmunity, or congenital Zika syndrome. Monocytes are primary ZIKV targets in humans and, in response to infection, release extracellular vesicles like exosomes. Exosomes mediate intercellular communication and are involved in the virus's ability to circumvent the immune response, promoting pathological processes. This study aimed to evaluate the role of monocyte exosomes in cell-to-cell viral transmission. We isolated exosomes from ZIKV-infected monocytes (Mø exo ZIKV) by differential ultracentrifugation and identified them by nanoparticle tracking analysis; transmission electron microscopy; and CD63, CD81, TSG101, and Alix detection by cytofluorometry. Purified exosome isolates were obtained by uncoupling from paramagnetic beads or by treatment with UV radiation and RNase A. We found that Mø exo ZIKV carry viral RNA and E/NS1 proteins and that their interaction with naïve cells favors viral transmission, infection, and cell differentiation/activation. These data suggest that Mø exo ZIKV are an efficient alternative pathway for ZIKV infection. Knowledge of these mechanisms contributes to understanding the pathogenesis of severe disease and to the development of new vaccines and therapies.
Insights
Zika virus (ZIKV) can spread through exosomes released by infected monocytes. These exosomes facilitate ZIKV transmission, infection, and cell activation, offering a new understanding of severe Zika disease.
Area of Science:
- Virology
- Immunology
- Cell Biology
Background:
- Zika virus (ZIKV) is an arthropod-borne virus causing severe neurological and developmental disorders.
- Monocytes are key targets for ZIKV, and their response involves releasing exosomes.
- Exosomes play a role in intercellular communication and immune evasion during viral infections.
Purpose of the Study:
- To investigate the role of exosomes derived from ZIKV-infected monocytes in viral transmission.
- To determine if these exosomes can mediate cell-to-cell spread of ZIKV.
Main Methods:
- Isolation of exosomes from ZIKV-infected human monocytes (Mø exo ZIKV) using differential ultracentrifugation.
- Characterization of exosomes via nanoparticle tracking analysis, transmission electron microscopy, and surface marker detection (CD63, CD81, TSG101, Alix).
- Purification of exosomes and assessment of their infectivity and impact on recipient cells.
Main Results:
- Mø exo ZIKV were confirmed to contain ZIKV RNA and E/NS1 proteins.
- Exposure of naïve cells to Mø exo ZIKV promoted viral transmission and infection.
- Interaction with Mø exo ZIKV led to recipient cell differentiation and activation.
Conclusions:
- Monocyte-derived exosomes serve as an efficient pathway for ZIKV cell-to-cell transmission.
- Understanding this transmission route is crucial for ZIKV pathogenesis research.
- These findings can inform the development of novel ZIKV vaccines and therapeutics.
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