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Detailed morphological characterisation of Hendra virus infection of different cell types using super-resolution and conventional imaging

BACKGROUND: Hendra virus (HeV) is a pleomorphic virus belonging to the Paramyxovirus family. Our long-term aim is to understand the process of assembly of HeV virions. As a first step, we sought to determine the most appropriate cell culture system with which to study this process, and then to use t...

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Autores principales: Monaghan, Paul, Green, Diane, Pallister, Jackie, Klein, Reuben, White, John, Williams, Catherine, McMillan, Paul, Tilley, Leann, Lampe, Marko, Hawes, Pippa, Wang, Lin-Fa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4254186/
https://www.ncbi.nlm.nih.gov/pubmed/25428656
http://dx.doi.org/10.1186/s12985-014-0200-5
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author Monaghan, Paul
Green, Diane
Pallister, Jackie
Klein, Reuben
White, John
Williams, Catherine
McMillan, Paul
Tilley, Leann
Lampe, Marko
Hawes, Pippa
Wang, Lin-Fa
author_facet Monaghan, Paul
Green, Diane
Pallister, Jackie
Klein, Reuben
White, John
Williams, Catherine
McMillan, Paul
Tilley, Leann
Lampe, Marko
Hawes, Pippa
Wang, Lin-Fa
author_sort Monaghan, Paul
collection PubMed
description BACKGROUND: Hendra virus (HeV) is a pleomorphic virus belonging to the Paramyxovirus family. Our long-term aim is to understand the process of assembly of HeV virions. As a first step, we sought to determine the most appropriate cell culture system with which to study this process, and then to use this model to define the morphology of the virus and identify the site of assembly by imaging key virus encoded proteins in infected cells. METHODS: A range of primary cells and immortalised cell lines were infected with HeV, fixed at various time points post-infection, labelled for HeV proteins and imaged by confocal, super-resolution and transmission electron microscopy. RESULTS: Significant differences were noted in viral protein distribution depending on the infected cell type. At 8 hpi HeV G protein was detected in the endoplasmic reticulum and M protein was seen predominantly in the nucleus in all cells tested. At 18 hpi, HeV-infected Vero cells showed M and G proteins throughout the cell and in transmission electron microscope (TEM) sections, in pleomorphic virus-like structures. In HeV infected MDBK, A549 and HeLa cells, HeV M protein was seen predominantly in the nucleus with G protein at the membrane. In HeV-infected primary bovine and porcine aortic endothelial cells and two bat-derived cell lines, HeV M protein was not seen at such high levels in the nucleus at any time point tested (8,12, 18, 24, 48 hpi) but was observed predominantly at the cell surface in a punctate pattern co-localised with G protein. These HeV M and G positive structures were confirmed as round HeV virions by TEM and super-resolution (SR) microscopy. SR imaging demonstrated for the first time sub-virion imaging of paramyxovirus proteins and the respective localisation of HeV G, M and N proteins within virions. CONCLUSION: These findings provide novel insights into the structure of HeV and show that for HeV imaging studies the choice of tissue culture cells may affect the experimental results. The results also indicate that HeV should be considered a predominantly round virus with a mean diameter of approximately 280 nm by TEM and 310 nm by SR imaging.
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spelling pubmed-42541862014-12-04 Detailed morphological characterisation of Hendra virus infection of different cell types using super-resolution and conventional imaging Monaghan, Paul Green, Diane Pallister, Jackie Klein, Reuben White, John Williams, Catherine McMillan, Paul Tilley, Leann Lampe, Marko Hawes, Pippa Wang, Lin-Fa Virol J Research BACKGROUND: Hendra virus (HeV) is a pleomorphic virus belonging to the Paramyxovirus family. Our long-term aim is to understand the process of assembly of HeV virions. As a first step, we sought to determine the most appropriate cell culture system with which to study this process, and then to use this model to define the morphology of the virus and identify the site of assembly by imaging key virus encoded proteins in infected cells. METHODS: A range of primary cells and immortalised cell lines were infected with HeV, fixed at various time points post-infection, labelled for HeV proteins and imaged by confocal, super-resolution and transmission electron microscopy. RESULTS: Significant differences were noted in viral protein distribution depending on the infected cell type. At 8 hpi HeV G protein was detected in the endoplasmic reticulum and M protein was seen predominantly in the nucleus in all cells tested. At 18 hpi, HeV-infected Vero cells showed M and G proteins throughout the cell and in transmission electron microscope (TEM) sections, in pleomorphic virus-like structures. In HeV infected MDBK, A549 and HeLa cells, HeV M protein was seen predominantly in the nucleus with G protein at the membrane. In HeV-infected primary bovine and porcine aortic endothelial cells and two bat-derived cell lines, HeV M protein was not seen at such high levels in the nucleus at any time point tested (8,12, 18, 24, 48 hpi) but was observed predominantly at the cell surface in a punctate pattern co-localised with G protein. These HeV M and G positive structures were confirmed as round HeV virions by TEM and super-resolution (SR) microscopy. SR imaging demonstrated for the first time sub-virion imaging of paramyxovirus proteins and the respective localisation of HeV G, M and N proteins within virions. CONCLUSION: These findings provide novel insights into the structure of HeV and show that for HeV imaging studies the choice of tissue culture cells may affect the experimental results. The results also indicate that HeV should be considered a predominantly round virus with a mean diameter of approximately 280 nm by TEM and 310 nm by SR imaging. BioMed Central 2014-11-27 /pmc/articles/PMC4254186/ /pubmed/25428656 http://dx.doi.org/10.1186/s12985-014-0200-5 Text en © Monaghan et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Monaghan, Paul
Green, Diane
Pallister, Jackie
Klein, Reuben
White, John
Williams, Catherine
McMillan, Paul
Tilley, Leann
Lampe, Marko
Hawes, Pippa
Wang, Lin-Fa
Detailed morphological characterisation of Hendra virus infection of different cell types using super-resolution and conventional imaging
title Detailed morphological characterisation of Hendra virus infection of different cell types using super-resolution and conventional imaging
title_full Detailed morphological characterisation of Hendra virus infection of different cell types using super-resolution and conventional imaging
title_fullStr Detailed morphological characterisation of Hendra virus infection of different cell types using super-resolution and conventional imaging
title_full_unstemmed Detailed morphological characterisation of Hendra virus infection of different cell types using super-resolution and conventional imaging
title_short Detailed morphological characterisation of Hendra virus infection of different cell types using super-resolution and conventional imaging
title_sort detailed morphological characterisation of hendra virus infection of different cell types using super-resolution and conventional imaging
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4254186/
https://www.ncbi.nlm.nih.gov/pubmed/25428656
http://dx.doi.org/10.1186/s12985-014-0200-5
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