Literature DB >> 15039536

The ultrastructure of the developing replication site in foot-and-mouth disease virus-infected BHK-38 cells.

Paul Monaghan1, Hannah Cook1, Terry Jackson1, Martin Ryan2, Tom Wileman1.   

Abstract

Foot-and-mouth disease virus (FMDV) is the type species of the Aphthovirus genus of the Picornaviridae: Infection by picornaviruses results in a major rearrangement of the host cell membranes to create vesicular structures where virus genome replication takes place. In this report, using fluorescence and electron microscopy, membrane rearrangements in the cytoplasm of FMDV-infected BHK-38 cells are documented. At 1.5-2.0 h post-infection, free ribosomes, fragmented rough endoplasmic reticulum, Golgi and smooth membrane-bound vesicles accumulated on one side of the nucleus. Newly synthesized viral RNA was localized to this region of the cell. The changes seen in FMDV-infected cells distinguish this virus from other members of the Picornaviridae, such as poliovirus. Firstly, the collapse of cellular organelles to one side of the cell has not previously been observed for other picornaviruses. Secondly, the membrane vesicles, induced by FMDV, appear distinct from those induced by other picornaviruses such as poliovirus and echovirus 11 since they are relatively few in number and do not aggregate into densely packed clusters. Additionally, the proportion of vesicles with double membranes is considerably lower in FMDV-infected cells. These differences did not result from the use of BHK-38 cells in this study, as infection of these cells by another picornavirus, bovine enterovirus (a close relative of poliovirus), resulted in morphological changes similar to those reported for poliovirus-infected cells. With conventional fixation, FMDV particles were not seen; however, following high-pressure freezing and freeze-substitution, many clusters of virus-like particles were seen.

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Year:  2004        PMID: 15039536     DOI: 10.1099/vir.0.19408-0

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  45 in total

1.  Integrity of the early secretory pathway promotes, but is not required for, severe acute respiratory syndrome coronavirus RNA synthesis and virus-induced remodeling of endoplasmic reticulum membranes.

Authors:  Kèvin Knoops; Cindy Swett-Tapia; Sjoerd H E van den Worm; Aartjan J W Te Velthuis; Abraham J Koster; A Mieke Mommaas; Eric J Snijder; Marjolein Kikkert
Journal:  J Virol       Date:  2009-11-04       Impact factor: 5.103

2.  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

Review 3.  Rewiring of cellular membrane homeostasis by picornaviruses.

Authors:  George A Belov; Elizabeth Sztul
Journal:  J Virol       Date:  2014-06-11       Impact factor: 5.103

4.  Foot-and-mouth disease virus genome replication is unaffected by inhibition of type III phosphatidylinositol-4-kinases.

Authors:  Eleni-Anna Loundras; Morgan R Herod; Mark Harris; Nicola J Stonehouse
Journal:  J Gen Virol       Date:  2016-06-20       Impact factor: 3.891

5.  Effects of foot-and-mouth disease virus nonstructural proteins on the structure and function of the early secretory pathway: 2BC but not 3A blocks endoplasmic reticulum-to-Golgi transport.

Authors:  Katy Moffat; Gareth Howell; Caroline Knox; Graham J Belsham; Paul Monaghan; Martin D Ryan; Thomas Wileman
Journal:  J Virol       Date:  2005-04       Impact factor: 5.103

6.  ACBD3-mediated recruitment of PI4KB to picornavirus RNA replication sites.

Authors:  Jun Sasaki; Kumiko Ishikawa; Minetaro Arita; Koki Taniguchi
Journal:  EMBO J       Date:  2011-11-29       Impact factor: 11.598

Review 7.  A guide to viral inclusions, membrane rearrangements, factories, and viroplasm produced during virus replication.

Authors:  Christopher Netherton; Katy Moffat; Elizabeth Brooks; Thomas Wileman
Journal:  Adv Virus Res       Date:  2007       Impact factor: 9.937

8.  A single amino acid substitution in the capsid of foot-and-mouth disease virus can increase acid lability and confer resistance to acid-dependent uncoating inhibition.

Authors:  Miguel A Martín-Acebes; Verónica Rincón; Rosario Armas-Portela; Mauricio G Mateu; Francisco Sobrino
Journal:  J Virol       Date:  2010-01-06       Impact factor: 5.103

9.  Deletion mutants of VPg reveal new cytopathology determinants in a picornavirus.

Authors:  Armando Arias; Celia Perales; Cristina Escarmís; Esteban Domingo
Journal:  PLoS One       Date:  2010-05-20       Impact factor: 3.240

10.  Feline calicivirus p32, p39 and p30 proteins localize to the endoplasmic reticulum to initiate replication complex formation.

Authors:  Dalan Bailey; William J Kaiser; Mike Hollinshead; Katy Moffat; Yasmin Chaudhry; Thomas Wileman; Stanislav V Sosnovtsev; Ian G Goodfellow
Journal:  J Gen Virol       Date:  2009-11-11       Impact factor: 3.891

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