RNA interference and single particle tracking analysis of hepatitis C virus endocytosis.

Hepatitis C virus (HCV) enters hepatocytes following a complex set of receptor interactions, culminating in internalization via clathrin-mediated endocytosis. However, aside from receptors, little is known about the cellular molecular requirements for infectious HCV entry. Therefore, we analyzed a s...

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Main Authors: Kelly E Coller, Kristi L Berger, Nicholas S Heaton, Jacob D Cooper, Rosa Yoon, Glenn Randall
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-12-01
Series:PLoS Pathogens
Online Access:https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1000702&type=printable
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author Kelly E Coller
Kristi L Berger
Nicholas S Heaton
Jacob D Cooper
Rosa Yoon
Glenn Randall
author_facet Kelly E Coller
Kristi L Berger
Nicholas S Heaton
Jacob D Cooper
Rosa Yoon
Glenn Randall
author_sort Kelly E Coller
collection DOAJ
description Hepatitis C virus (HCV) enters hepatocytes following a complex set of receptor interactions, culminating in internalization via clathrin-mediated endocytosis. However, aside from receptors, little is known about the cellular molecular requirements for infectious HCV entry. Therefore, we analyzed a siRNA library that targets 140 cellular membrane trafficking genes to identify host genes required for infectious HCV production and HCV pseudoparticle entry. This approach identified 16 host cofactors of HCV entry that function primarily in clathrin-mediated endocytosis, including components of the clathrin endocytosis machinery, actin polymerization, receptor internalization and sorting, and endosomal acidification. We next developed single particle tracking analysis of highly infectious fluorescent HCV particles to examine the co-trafficking of HCV virions with cellular cofactors of endocytosis. We observe multiple, sequential interactions of HCV virions with the actin cytoskeleton, including retraction along filopodia, actin nucleation during internalization, and migration of internalized particles along actin stress fibers. HCV co-localizes with clathrin and the ubiquitin ligase c-Cbl prior to internalization. Entering HCV particles are associated with the receptor molecules CD81 and the tight junction protein, claudin-1; however, HCV-claudin-1 interactions were not restricted to Huh-7.5 cell-cell junctions. Surprisingly, HCV internalization generally occurred outside of Huh-7.5 cell-cell junctions, which may reflect the poorly polarized nature of current HCV cell culture models. Following internalization, HCV particles transport with GFP-Rab5a positive endosomes, which is consistent with trafficking to the early endosome. This study presents technical advances for imaging HCV entry, in addition to identifying new host cofactors of HCV infection, some of which may be antiviral targets.
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spelling doaj-art-31e686d87fbb4d0696bd63a2d6d46f6f2025-08-20T02:02:01ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742009-12-01512e100070210.1371/journal.ppat.1000702RNA interference and single particle tracking analysis of hepatitis C virus endocytosis.Kelly E CollerKristi L BergerNicholas S HeatonJacob D CooperRosa YoonGlenn RandallHepatitis C virus (HCV) enters hepatocytes following a complex set of receptor interactions, culminating in internalization via clathrin-mediated endocytosis. However, aside from receptors, little is known about the cellular molecular requirements for infectious HCV entry. Therefore, we analyzed a siRNA library that targets 140 cellular membrane trafficking genes to identify host genes required for infectious HCV production and HCV pseudoparticle entry. This approach identified 16 host cofactors of HCV entry that function primarily in clathrin-mediated endocytosis, including components of the clathrin endocytosis machinery, actin polymerization, receptor internalization and sorting, and endosomal acidification. We next developed single particle tracking analysis of highly infectious fluorescent HCV particles to examine the co-trafficking of HCV virions with cellular cofactors of endocytosis. We observe multiple, sequential interactions of HCV virions with the actin cytoskeleton, including retraction along filopodia, actin nucleation during internalization, and migration of internalized particles along actin stress fibers. HCV co-localizes with clathrin and the ubiquitin ligase c-Cbl prior to internalization. Entering HCV particles are associated with the receptor molecules CD81 and the tight junction protein, claudin-1; however, HCV-claudin-1 interactions were not restricted to Huh-7.5 cell-cell junctions. Surprisingly, HCV internalization generally occurred outside of Huh-7.5 cell-cell junctions, which may reflect the poorly polarized nature of current HCV cell culture models. Following internalization, HCV particles transport with GFP-Rab5a positive endosomes, which is consistent with trafficking to the early endosome. This study presents technical advances for imaging HCV entry, in addition to identifying new host cofactors of HCV infection, some of which may be antiviral targets.https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1000702&type=printable
spellingShingle Kelly E Coller
Kristi L Berger
Nicholas S Heaton
Jacob D Cooper
Rosa Yoon
Glenn Randall
RNA interference and single particle tracking analysis of hepatitis C virus endocytosis.
PLoS Pathogens
title RNA interference and single particle tracking analysis of hepatitis C virus endocytosis.
title_full RNA interference and single particle tracking analysis of hepatitis C virus endocytosis.
title_fullStr RNA interference and single particle tracking analysis of hepatitis C virus endocytosis.
title_full_unstemmed RNA interference and single particle tracking analysis of hepatitis C virus endocytosis.
title_short RNA interference and single particle tracking analysis of hepatitis C virus endocytosis.
title_sort rna interference and single particle tracking analysis of hepatitis c virus endocytosis
url https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1000702&type=printable
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