Efficient replication of pneumonia virus of mice (PVM) in a mouse macrophage cell line

<p>Abstract</p> <p>Pneumonia virus of mice (PVM; family <it>Paramyxoviridae</it>, subfamily <it>Pneumovirinae</it>) is a natural respiratory pathogen of rodent species and an important new model for the study of severe viral bronchiolitis and pneumonia. Howe...

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Main Authors: Martin Brittany V, Bonville Cynthia A, Schellens Ingrid MM, Dyer Kimberly D, Domachowske Joseph B, Rosenberg Helene F
Format: Article
Language:English
Published: BMC 2007-06-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/4/1/48
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spelling doaj-ee9c4f5bb53c4c4eb99ca1d22d0737c92020-11-24T21:01:37ZengBMCVirology Journal1743-422X2007-06-01414810.1186/1743-422X-4-48Efficient replication of pneumonia virus of mice (PVM) in a mouse macrophage cell lineMartin Brittany VBonville Cynthia ASchellens Ingrid MMDyer Kimberly DDomachowske Joseph BRosenberg Helene F<p>Abstract</p> <p>Pneumonia virus of mice (PVM; family <it>Paramyxoviridae</it>, subfamily <it>Pneumovirinae</it>) is a natural respiratory pathogen of rodent species and an important new model for the study of severe viral bronchiolitis and pneumonia. However, despite high virus titers typically detected in infected mouse lung tissue <it>in vivo</it>, cell lines used routinely for virus propagation <it>in vitro </it>are not highly susceptible to PVM infection. We have evaluated several rodent and primate cell lines for susceptibility to PVM infection, and detected highest virus titers from infection of the mouse monocyte-macrophage RAW 264.7 cell line. Additionally, virus replication in RAW 264.7 cells induces the synthesis and secretion of proinflammatory cytokines relevant to respiratory virus disease, including tumor necrosis factor-α (TNF-α), interferon-β (IFN-β), macrophage inflammatory proteins 1α and 1β (MIP-1α and MIP-1β) and the functional homolog of human IL-8, mouse macrophage inflammatory peptide-2 (MIP-2). Identification and characterization of a rodent cell line that supports the replication of PVM and induces the synthesis of disease-related proinflammatory mediators will facilitate studies of molecular mechanisms of viral pathogenesis that will complement and expand on findings from mouse model systems.</p> http://www.virologyj.com/content/4/1/48
collection DOAJ
language English
format Article
sources DOAJ
author Martin Brittany V
Bonville Cynthia A
Schellens Ingrid MM
Dyer Kimberly D
Domachowske Joseph B
Rosenberg Helene F
spellingShingle Martin Brittany V
Bonville Cynthia A
Schellens Ingrid MM
Dyer Kimberly D
Domachowske Joseph B
Rosenberg Helene F
Efficient replication of pneumonia virus of mice (PVM) in a mouse macrophage cell line
Virology Journal
author_facet Martin Brittany V
Bonville Cynthia A
Schellens Ingrid MM
Dyer Kimberly D
Domachowske Joseph B
Rosenberg Helene F
author_sort Martin Brittany V
title Efficient replication of pneumonia virus of mice (PVM) in a mouse macrophage cell line
title_short Efficient replication of pneumonia virus of mice (PVM) in a mouse macrophage cell line
title_full Efficient replication of pneumonia virus of mice (PVM) in a mouse macrophage cell line
title_fullStr Efficient replication of pneumonia virus of mice (PVM) in a mouse macrophage cell line
title_full_unstemmed Efficient replication of pneumonia virus of mice (PVM) in a mouse macrophage cell line
title_sort efficient replication of pneumonia virus of mice (pvm) in a mouse macrophage cell line
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2007-06-01
description <p>Abstract</p> <p>Pneumonia virus of mice (PVM; family <it>Paramyxoviridae</it>, subfamily <it>Pneumovirinae</it>) is a natural respiratory pathogen of rodent species and an important new model for the study of severe viral bronchiolitis and pneumonia. However, despite high virus titers typically detected in infected mouse lung tissue <it>in vivo</it>, cell lines used routinely for virus propagation <it>in vitro </it>are not highly susceptible to PVM infection. We have evaluated several rodent and primate cell lines for susceptibility to PVM infection, and detected highest virus titers from infection of the mouse monocyte-macrophage RAW 264.7 cell line. Additionally, virus replication in RAW 264.7 cells induces the synthesis and secretion of proinflammatory cytokines relevant to respiratory virus disease, including tumor necrosis factor-α (TNF-α), interferon-β (IFN-β), macrophage inflammatory proteins 1α and 1β (MIP-1α and MIP-1β) and the functional homolog of human IL-8, mouse macrophage inflammatory peptide-2 (MIP-2). Identification and characterization of a rodent cell line that supports the replication of PVM and induces the synthesis of disease-related proinflammatory mediators will facilitate studies of molecular mechanisms of viral pathogenesis that will complement and expand on findings from mouse model systems.</p>
url http://www.virologyj.com/content/4/1/48
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