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Vaccinia Virus Infection Requires Maturation of Macropinosomes
The prototypic poxvirus, vaccinia virus (VACV), occurs in two infectious forms, mature virions (MVs) and extracellular virions (EVs). Both enter HeLa cells by inducing macropinocytic uptake. Using confocal microscopy, live‐cell imaging, targeted RNAi screening and perturbants of endosome maturation,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons A/S
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973667/ https://www.ncbi.nlm.nih.gov/pubmed/25869659 http://dx.doi.org/10.1111/tra.12290 |
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author | Rizopoulos, Zaira Balistreri, Giuseppe Kilcher, Samuel Martin, Caroline K. Syedbasha, Mohammedyaseen Helenius, Ari Mercer, Jason |
author_facet | Rizopoulos, Zaira Balistreri, Giuseppe Kilcher, Samuel Martin, Caroline K. Syedbasha, Mohammedyaseen Helenius, Ari Mercer, Jason |
author_sort | Rizopoulos, Zaira |
collection | PubMed |
description | The prototypic poxvirus, vaccinia virus (VACV), occurs in two infectious forms, mature virions (MVs) and extracellular virions (EVs). Both enter HeLa cells by inducing macropinocytic uptake. Using confocal microscopy, live‐cell imaging, targeted RNAi screening and perturbants of endosome maturation, we analyzed the properties and maturation pathway of the macropinocytic vacuoles containing VACV MVs in HeLa cells. The vacuoles first acquired markers of early endosomes [Rab5, early endosome antigen 1 and phosphatidylinositol(3)P]. Prior to release of virus cores into the cytoplasm, they contained markers of late endosomes and lysosomes (Rab7a, lysosome‐associated membrane protein 1 and sorting nexin 3). RNAi screening of endocytic cell factors emphasized the importance of late compartments for VACV infection. Follow‐up perturbation analysis showed that infection required Rab7a and PIKfyve, confirming that VACV is a late‐penetrating virus dependent on macropinosome maturation. VACV EV infection was inhibited by depletion of many of the same factors, indicating that both infectious particle forms share the need for late vacuolar conditions for penetration. [Image: see text] |
format | Online Article Text |
id | pubmed-4973667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons A/S |
record_format | MEDLINE/PubMed |
spelling | pubmed-49736672016-08-17 Vaccinia Virus Infection Requires Maturation of Macropinosomes Rizopoulos, Zaira Balistreri, Giuseppe Kilcher, Samuel Martin, Caroline K. Syedbasha, Mohammedyaseen Helenius, Ari Mercer, Jason Traffic Original Articles The prototypic poxvirus, vaccinia virus (VACV), occurs in two infectious forms, mature virions (MVs) and extracellular virions (EVs). Both enter HeLa cells by inducing macropinocytic uptake. Using confocal microscopy, live‐cell imaging, targeted RNAi screening and perturbants of endosome maturation, we analyzed the properties and maturation pathway of the macropinocytic vacuoles containing VACV MVs in HeLa cells. The vacuoles first acquired markers of early endosomes [Rab5, early endosome antigen 1 and phosphatidylinositol(3)P]. Prior to release of virus cores into the cytoplasm, they contained markers of late endosomes and lysosomes (Rab7a, lysosome‐associated membrane protein 1 and sorting nexin 3). RNAi screening of endocytic cell factors emphasized the importance of late compartments for VACV infection. Follow‐up perturbation analysis showed that infection required Rab7a and PIKfyve, confirming that VACV is a late‐penetrating virus dependent on macropinosome maturation. VACV EV infection was inhibited by depletion of many of the same factors, indicating that both infectious particle forms share the need for late vacuolar conditions for penetration. [Image: see text] John Wiley & Sons A/S 2015-05-06 2015-08 /pmc/articles/PMC4973667/ /pubmed/25869659 http://dx.doi.org/10.1111/tra.12290 Text en © 2015 The Authors. Traffic published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Rizopoulos, Zaira Balistreri, Giuseppe Kilcher, Samuel Martin, Caroline K. Syedbasha, Mohammedyaseen Helenius, Ari Mercer, Jason Vaccinia Virus Infection Requires Maturation of Macropinosomes |
title | Vaccinia Virus Infection Requires Maturation of Macropinosomes |
title_full | Vaccinia Virus Infection Requires Maturation of Macropinosomes |
title_fullStr | Vaccinia Virus Infection Requires Maturation of Macropinosomes |
title_full_unstemmed | Vaccinia Virus Infection Requires Maturation of Macropinosomes |
title_short | Vaccinia Virus Infection Requires Maturation of Macropinosomes |
title_sort | vaccinia virus infection requires maturation of macropinosomes |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973667/ https://www.ncbi.nlm.nih.gov/pubmed/25869659 http://dx.doi.org/10.1111/tra.12290 |
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