Challenges of culturing human norovirus in three-dimensional organoid intestinal cell culture models.
Human noroviruses are the most common cause of acute gastroenteritis worldwide. Recently, cell culture systems have been described using either human embryonic intestinal epithelial cells (Int-407) or human epithelial colorectal adenocarcinoma cells (Caco-2) growing on collagen-I porous micro carrie...
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doaj-53633822d36b4143941427bcb0281fae2020-11-25T01:56:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0186e6348510.1371/journal.pone.0063485Challenges of culturing human norovirus in three-dimensional organoid intestinal cell culture models.Efstathia PapafragkouJoanne HewittGeun Woo ParkGail GreeningJan VinjéHuman noroviruses are the most common cause of acute gastroenteritis worldwide. Recently, cell culture systems have been described using either human embryonic intestinal epithelial cells (Int-407) or human epithelial colorectal adenocarcinoma cells (Caco-2) growing on collagen-I porous micro carrier beads in a rotating bioreactor under conditions of physiological fluid shear. Here, we describe the efforts from two independent laboratories to implement this three dimensional (3D) cell culture system for the replication of norovirus. Int-407 and Caco-2 were grown in a rotating bioreactor for up to 28 days. Prior to infection, cells were screened for the presence of microvilli by electron microscopy and stained for junction proteins (zonula occludens-1, claudin-1, and β-catenin). Differentiated 3D cells were transferred to 24-well plates and infected with bacteria-free filtrates of various norovirus genotypes (GI.1, GI.3, GI.8, GII.2, GII.4, GII.7, and GII.8). At 12 h, 24 h, and 48 h post inoculation, viral RNA from both cells and supernatants were collected and analyzed for norovirus RNA by real-time reverse transcription PCR. Despite observations of high expression of junction proteins and microvilli development in stained thin sections, our data suggest no significant increase in viral titer based on norovirus RNA copy number during the first 48 h after inoculation for the different samples and virus culture conditions tested. Our combined efforts demonstrate that 3D cell culture models using Int-407 or Caco-2 cells do not support norovirus replication and highlight the complexity and difficulty of developing a reproducible in vitro cell culture system for human norovirus.http://europepmc.org/articles/PMC3670855?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Efstathia Papafragkou Joanne Hewitt Geun Woo Park Gail Greening Jan Vinjé |
spellingShingle |
Efstathia Papafragkou Joanne Hewitt Geun Woo Park Gail Greening Jan Vinjé Challenges of culturing human norovirus in three-dimensional organoid intestinal cell culture models. PLoS ONE |
author_facet |
Efstathia Papafragkou Joanne Hewitt Geun Woo Park Gail Greening Jan Vinjé |
author_sort |
Efstathia Papafragkou |
title |
Challenges of culturing human norovirus in three-dimensional organoid intestinal cell culture models. |
title_short |
Challenges of culturing human norovirus in three-dimensional organoid intestinal cell culture models. |
title_full |
Challenges of culturing human norovirus in three-dimensional organoid intestinal cell culture models. |
title_fullStr |
Challenges of culturing human norovirus in three-dimensional organoid intestinal cell culture models. |
title_full_unstemmed |
Challenges of culturing human norovirus in three-dimensional organoid intestinal cell culture models. |
title_sort |
challenges of culturing human norovirus in three-dimensional organoid intestinal cell culture models. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2014-01-01 |
description |
Human noroviruses are the most common cause of acute gastroenteritis worldwide. Recently, cell culture systems have been described using either human embryonic intestinal epithelial cells (Int-407) or human epithelial colorectal adenocarcinoma cells (Caco-2) growing on collagen-I porous micro carrier beads in a rotating bioreactor under conditions of physiological fluid shear. Here, we describe the efforts from two independent laboratories to implement this three dimensional (3D) cell culture system for the replication of norovirus. Int-407 and Caco-2 were grown in a rotating bioreactor for up to 28 days. Prior to infection, cells were screened for the presence of microvilli by electron microscopy and stained for junction proteins (zonula occludens-1, claudin-1, and β-catenin). Differentiated 3D cells were transferred to 24-well plates and infected with bacteria-free filtrates of various norovirus genotypes (GI.1, GI.3, GI.8, GII.2, GII.4, GII.7, and GII.8). At 12 h, 24 h, and 48 h post inoculation, viral RNA from both cells and supernatants were collected and analyzed for norovirus RNA by real-time reverse transcription PCR. Despite observations of high expression of junction proteins and microvilli development in stained thin sections, our data suggest no significant increase in viral titer based on norovirus RNA copy number during the first 48 h after inoculation for the different samples and virus culture conditions tested. Our combined efforts demonstrate that 3D cell culture models using Int-407 or Caco-2 cells do not support norovirus replication and highlight the complexity and difficulty of developing a reproducible in vitro cell culture system for human norovirus. |
url |
http://europepmc.org/articles/PMC3670855?pdf=render |
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