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Table 1 Use of exosomes in the detection of the viral infection

From: A state-of-the-art review of the recent advances in exosome isolation and detection methods in viral infection

Viral infection

Exosome isolation method

Exosomes detection method

Explain

References

HIV-1

Ultracentrifugation

Western blotting

Regarding HIV-1 gene transcription and replication, the Tat is crucial. Overall, our findings demonstrate that a sizeable amount of Tat is released and present in exosomes, which may aid in the stability of extracellular Tat and increase the variety of cells it may infect

[121]

SARS-CoV-2

Microfluidics

RADx-Rad exosome-based technologies

The RADx-Rad program was to accelerate the development of exRNAs and EVs as potential therapeutics and diagnostics. In addition to detecting SARS-CoV-2, the RADx-Rad exosome-based technologies program would also be able to identify prognostic indicators that may signal a propensity toward developing severe illness or PASC

[129, 131]

HPV-OPC

Acoustofluidic platform

Droplet digital PCR (ddPCR)

Isolated saliva samples include high-purity exosomes since the particles contain known exosomal protein biomarkers and have the anticipated exosomal size and form. Exosomal miRNA was quantified using ddPCR for miRNAs, and the results showed that the quantity of miRNA in acoustofluidic-separated samples was more than in the sample isolated by differential centrifugation

[134]

HBV

ExoQuick-TC exosome extraction kit

Nanoparticle tracking analysis (NTA)

Patients who test negative for serum HBV-DNA but have a strong suspicion of HBV infection may benefit from using exosomal HBV-DNA. Thus, tracking the amount of HBV-DNA in exosomes may help select therapy to stop the illness from developing into LC and cancer and immediately and properly represent the onset and progression of the disease

[121]

HCV

D63 immuno-magnetic separation

Western blotting (for CD9 and CD81), electron microscopy, and NTA

Researchers found that in HCV J6/JFH-1 infected Huh7.5 cell supernatants, there were almost seven times as many free HCV viral particles as there were exosome particles in the same volume, and in HCV infected patient serum samples, the ratio was about four times as high

[147]

HSV-1

Ultracentrifugation

Western blotting

Recurrent HSK suggests that HSV-1 is latent in tear exosomes and that they may play a role in HSV-1 transmission. This research also confirms the exosomal route as a viable HSV-1 gene transfer, opening up new avenues for therapeutic intervention and therapy of recurrent HSK

[149]