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Generation of fluorescent HCV pseudoparticles to study early viral entry events- involvement of Rab1a in HCV entry

Understanding the early events in viral biology holds the key to the development of potent preventives. In this study, fluorescent hepatitis C virus pseudoparticles (HCVpp) have been generated where the envelope glycoprotein of Hepatitis C virus (HCV) has an EGFP tag. Using these pseudoparticles, en...

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Detalles Bibliográficos
Autores principales: Bhattacharjee, Chayan, Mukhopadhyay, Aparna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer India 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9275390/
https://www.ncbi.nlm.nih.gov/pubmed/35855963
http://dx.doi.org/10.1007/s13337-022-00770-2
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author Bhattacharjee, Chayan
Mukhopadhyay, Aparna
author_facet Bhattacharjee, Chayan
Mukhopadhyay, Aparna
author_sort Bhattacharjee, Chayan
collection PubMed
description Understanding the early events in viral biology holds the key to the development of potent preventives. In this study, fluorescent hepatitis C virus pseudoparticles (HCVpp) have been generated where the envelope glycoprotein of Hepatitis C virus (HCV) has an EGFP tag. Using these pseudoparticles, entry assays were conducted where their entry was tracked via confocal microscopy. Using this system, fusion of host and viral membranes is predicted to occur within 15 min of HCV entry. Using cells with a knockdown for Rab1a, HCV trafficking was observed to be altered, indicating a role of Rab1a in HCV trafficking. In conclusion, this study reports the generation and use of fluorescent HCVpp which may be used to understand the early events of viral entry. This system may be adapted for the study of other enveloped viruses as well.
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spelling pubmed-92753902022-07-14 Generation of fluorescent HCV pseudoparticles to study early viral entry events- involvement of Rab1a in HCV entry Bhattacharjee, Chayan Mukhopadhyay, Aparna Virusdisease Original Article Understanding the early events in viral biology holds the key to the development of potent preventives. In this study, fluorescent hepatitis C virus pseudoparticles (HCVpp) have been generated where the envelope glycoprotein of Hepatitis C virus (HCV) has an EGFP tag. Using these pseudoparticles, entry assays were conducted where their entry was tracked via confocal microscopy. Using this system, fusion of host and viral membranes is predicted to occur within 15 min of HCV entry. Using cells with a knockdown for Rab1a, HCV trafficking was observed to be altered, indicating a role of Rab1a in HCV trafficking. In conclusion, this study reports the generation and use of fluorescent HCVpp which may be used to understand the early events of viral entry. This system may be adapted for the study of other enveloped viruses as well. Springer India 2022-07-11 2022-06 /pmc/articles/PMC9275390/ /pubmed/35855963 http://dx.doi.org/10.1007/s13337-022-00770-2 Text en © The Author(s), under exclusive licence to Indian Virological Society 2022
spellingShingle Original Article
Bhattacharjee, Chayan
Mukhopadhyay, Aparna
Generation of fluorescent HCV pseudoparticles to study early viral entry events- involvement of Rab1a in HCV entry
title Generation of fluorescent HCV pseudoparticles to study early viral entry events- involvement of Rab1a in HCV entry
title_full Generation of fluorescent HCV pseudoparticles to study early viral entry events- involvement of Rab1a in HCV entry
title_fullStr Generation of fluorescent HCV pseudoparticles to study early viral entry events- involvement of Rab1a in HCV entry
title_full_unstemmed Generation of fluorescent HCV pseudoparticles to study early viral entry events- involvement of Rab1a in HCV entry
title_short Generation of fluorescent HCV pseudoparticles to study early viral entry events- involvement of Rab1a in HCV entry
title_sort generation of fluorescent hcv pseudoparticles to study early viral entry events- involvement of rab1a in hcv entry
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9275390/
https://www.ncbi.nlm.nih.gov/pubmed/35855963
http://dx.doi.org/10.1007/s13337-022-00770-2
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