Table 1.
The viral proteins known to regulate exosomes biogenesis.
| Virus type | Virus name | Viral components | Effector | Function and mechanism | Reference |
|---|---|---|---|---|---|
| RNA VIRUS | HIV-1 (+ssRNA) | Accessory protein Nef | — | Nef expression reduces the sorting of CD4 and MHC class 1 molecules into exosomes | (de Carvalho et al., 2014) |
| Nef expression in monocytes alters miRNA distribution within exosomes and cells | (Aqil et al., 2014) | ||||
| EBOV (-ssRNA) | Matrix protein VP40 | — | VP40 may increase the production of exosomes by upregulating some ESCRT machinery components. | (Pleet et al., 2016) | |
| cyclin D1 | VP40 reduces the number of while increasing the size of secreted EVs, especially at G0 phase, though its modulation of the cell cycle via upregulation cycling D1 expression. | (Pleet et al., 2018) | |||
| HAV (+ssRNA) | Structural protein pX | Alix | PX transports foreign protein and virus particles into MVBs prior to their release via exosomes by interacting with Alix directly. | (Feng et al., 2013; Jiang et al., 2020) | |
| DNA VIRUS | HHV-1 (dsDNA) | gB | DR molecules | Glycoprotein B binds to DR, and ubiquitinated gB transfers DR-gB complexes into the exosomes. | (Temme et al., 2010) |
| Accessory protein γ134.5 | — | The deletion of viral γ134.5 gene markedly attenuates HSV-induced exosome secretion. | (Heikkilä et al., 2016) | ||
| HHV-4 (dsDNA) | LMP1 | SDC2 and SYTL4 | LMP1 increases exosome secretion by upregulating SDC2 and SYTL4 in cells and the interaction between SDC2 and syntenin. | (Liao et al., 2020) | |
| HBV (dsDNA) | HBx | nSMASE2 and CD9, CD81, and CD63 | HBx increases exosome secretion by upregulating the activity and mRNA level of nSMase2 and interacting with the exosomal biomarkers CD9, CD81, and nSMase2. | (Kapoor et al., 2017); | |
|
HBx enhances the transportation of A3G protein into the exosomes. | (Chen et al., 2017) | |||
| PRIONS | protein-based infectious agent | PRNP | Caveolin-1 | PRNP increases exosome secretion by inhibiting the caveolin-1-activated autophage pathway. | (Dias et al., 2016) |