Literature DB >> 18753210

Foot-and-mouth disease virus, but not bovine enterovirus, targets the host cell cytoskeleton via the nonstructural protein 3Cpro.

Hannah Armer1, Katy Moffat, Thomas Wileman, Graham J Belsham, Terry Jackson, W Paul Duprex, Martin Ryan, Paul Monaghan.   

Abstract

Foot-and-mouth disease virus (FMDV), a member of the Picornaviridae, is a pathogen of cloven-hoofed animals and causes a disease of major economic importance. Picornavirus-infected cells show changes in cell morphology and rearrangement of cytoplasmic membranes, which are a consequence of virus replication. We show here, by confocal immunofluorescence and electron microscopy, that the changes in morphology of FMDV-infected cells involve changes in the distribution of microtubule and intermediate filament components during infection. Despite the continued presence of centrosomes in infected cells, there is a loss of tethering of microtubules to the microtubule organizing center (MTOC) region. Loss of labeling for gamma-tubulin, but not pericentrin, from the MTOC suggests a targeting of gamma-tubulin (or associated proteins) rather than a total breakdown in MTOC structure. The identity of the FMDV protein(s) responsible was determined by the expression of individual viral nonstructural proteins and their precursors in uninfected cells. We report that the only viral nonstructural protein able to reproduce the loss of gamma-tubulin from the MTOC and the loss of integrity of the microtubule system is FMDV 3C(pro). In contrast, infection of cells with another picornavirus, bovine enterovirus, did not affect gamma-tubulin distribution, and the microtubule network remained relatively unaffected.

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Year:  2008        PMID: 18753210      PMCID: PMC2573224          DOI: 10.1128/JVI.00907-08

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  82 in total

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Journal:  J Virol       Date:  1997-02       Impact factor: 5.103

4.  Inhibition of the secretory pathway by foot-and-mouth disease virus 2BC protein is reproduced by coexpression of 2B with 2C, and the site of inhibition is determined by the subcellular location of 2C.

Authors:  Katy Moffat; Caroline Knox; Gareth Howell; Sarah J Clark; H Yang; Graham J Belsham; Martin Ryan; Thomas Wileman
Journal:  J Virol       Date:  2006-11-22       Impact factor: 5.103

5.  African swine fever virus induces filopodia-like projections at the plasma membrane.

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Journal:  Cell Microbiol       Date:  2006-07-26       Impact factor: 3.715

Review 6.  A guide to viral inclusions, membrane rearrangements, factories, and viroplasm produced during virus replication.

Authors:  Christopher Netherton; Katy Moffat; Elizabeth Brooks; Thomas Wileman
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7.  Vaccinia virus-induced microtubule-dependent cellular rearrangements.

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8.  Cellular origin and ultrastructure of membranes induced during poliovirus infection.

Authors:  A Schlegel; T H Giddings; M S Ladinsky; K Kirkegaard
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9.  Membrane permeabilization by poliovirus proteins 2B and 2BC.

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10.  NEDD1-dependent recruitment of the gamma-tubulin ring complex to the centrosome is necessary for centriole duplication and spindle assembly.

Authors:  Laurence Haren; Marie-Hélène Remy; Ingrid Bazin; Isabelle Callebaut; Michel Wright; Andreas Merdes
Journal:  J Cell Biol       Date:  2006-02-06       Impact factor: 10.539

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  21 in total

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Journal:  J Virol       Date:  2012-02-01       Impact factor: 5.103

Review 2.  Microtubule Regulation and Function during Virus Infection.

Authors:  Mojgan H Naghavi; Derek Walsh
Journal:  J Virol       Date:  2017-07-27       Impact factor: 5.103

3.  Cellular Vimentin Interacts with Foot-and-Mouth Disease Virus Nonstructural Protein 3A and Negatively Modulates Viral Replication.

Authors:  Xueqing Ma; Ying Ling; Pinghua Li; Pu Sun; Yimei Cao; Xingwen Bai; Kun Li; Yuanfang Fu; Jing Zhang; Dong Li; Huifang Bao; Yingli Chen; Zhiyong Li; Yonggang Wang; Zengjun Lu; Zaixin Liu
Journal:  J Virol       Date:  2020-07-30       Impact factor: 5.103

4.  Comparison of strategies for the production of FMDV empty capsids using the baculovirus vector system.

Authors:  V Ruiz; A C Mignaqui; M C Nuñez; E Reytor; J M Escribano; A Wigdorovitz
Journal:  Mol Biotechnol       Date:  2014-11       Impact factor: 2.695

5.  Suppression of injuries caused by a lytic RNA virus (mengovirus) and their uncoupling from viral reproduction by mutual cell/virus disarmament.

Authors:  Olga V Mikitas; Yuri Y Ivin; Sergey A Golyshev; Natalia V Povarova; Svetlana I Galkina; Olga Y Pletjushkina; Elena S Nadezhdina; Anatoly P Gmyl; Vadim I Agol
Journal:  J Virol       Date:  2012-03-21       Impact factor: 5.103

6.  Foot-and-mouth disease virus nonstructural protein 2C interacts with Beclin1, modulating virus replication.

Authors:  D P Gladue; V O'Donnell; R Baker-Branstetter; L G Holinka; J M Pacheco; I Fernandez-Sainz; Z Lu; E Brocchi; B Baxt; M E Piccone; L Rodriguez; M V Borca
Journal:  J Virol       Date:  2012-08-29       Impact factor: 5.103

7.  Cell susceptibility to baculovirus transduction and echovirus infection is modified by protein kinase C phosphorylation and vimentin organization.

Authors:  Paula Turkki; Kaisa-Emilia Makkonen; Moona Huttunen; Johanna P Laakkonen; Seppo Ylä-Herttuala; Kari J Airenne; Varpu Marjomäki
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8.  Sumoylation-promoted enterovirus 71 3C degradation correlates with a reduction in viral replication and cell apoptosis.

Authors:  Shu-Chuan Chen; Luan-Yin Chang; Yi-Wei Wang; Yi-Chun Chen; Kuo-Feng Weng; Shin-Ru Shih; Hsiu-Ming Shih
Journal:  J Biol Chem       Date:  2011-07-22       Impact factor: 5.157

9.  ICP0 dismantles microtubule networks in herpes simplex virus-infected cells.

Authors:  Mingyu Liu; Edward E Schmidt; William P Halford
Journal:  PLoS One       Date:  2010-06-08       Impact factor: 3.240

10.  Foot-and-mouth disease virus modulates cellular vimentin for virus survival.

Authors:  D P Gladue; V O'Donnell; R Baker-Branstetter; L G Holinka; J M Pacheco; I Fernández Sainz; Z Lu; X Ambroggio; L Rodriguez; M V Borca
Journal:  J Virol       Date:  2013-04-10       Impact factor: 5.103

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