4.7 Article

Characterization and Involvement of Exosomes Originating from Chikungunya Virus-Infected Epithelial Cells in the Transmission of Infectious Viral Elements

Journal

Publisher

MDPI
DOI: 10.3390/ijms232012117

Keywords

chikungunya virus (CHIKV); extracellular vesicles; EVs; exosomes; cell-to-cell transmission; infectious viral elements

Funding

  1. Research Council of Norway [250443]
  2. Research and Graduate Studies, Khon Kaen University, Thailand [RP65-8/001]
  3. Faculty of Medicine, Khon Kaen University
  4. DENCLIM project (the Research Council of Norway) [281077]

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The Chikungunya virus (CHIKV) is a mosquito-borne alphavirus that causes chikungunya disease. Recent studies have found that extracellular vesicles, including exosomes, play an important role in the infection and transmission of CHIKV. Infected epithelial cells release exosomes containing CHIKV RNA and proteins, which can infect other cells.
The Chikungunya virus (CHIKV) is a mosquito-borne alphavirus that affects the world's popula-tion with chikungunya disease. Adaptation of the viral life cycle to their host cells' environment is a key step for establishing their infection and pathogenesis. Recently, the accumulating evidence advocates a principal role of extracellular vesicles (EVs), including exosomes, in both the infection and pathogenesis of infectious diseases. However, the participation of exosomes in CHIKV infec-tion and transmission is not well clarified. Here, we demonstrated that the CHIKV RNA and pro-teins were captured in exosomes, which were released by viral-infected epithelial cells. A viral genomic element in the isolated exosomes was infectious to naive mammalian epithelial cells. The assay of particle size distribution and transmission electron microscopy (TEM) revealed CHIKV-derived exosomes with a size range from 50 to 250 nm. Treatments with RNase A, Triton X-100, and immunoglobulin G antibodies from CHIKV-positive patient plasma indicated that in-fectious viral elements are encompassed inside the exosomes. Interestingly, our viral plaque for-mation also exhibited that infectious viral elements might be securely transmitted to neighboring cells by a secreted exosomal pathway. Taken together, our recent findings emphasize the evidence for a complementary means of CHIKV infection and suggest the role of exosome-mediated CHIKV transmission.

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