Mechanism of Collapse of Endoplasmic Reticulum Cisternae During African Swine Fever Virus Infection

被引:15
作者
Windsor, Miriam [1 ]
Hawes, Philippa [1 ]
Monaghan, Paul [1 ,2 ]
Snapp, Erik [3 ]
Salas, Maria L. [4 ]
Rodriguez, Javier M. [5 ]
Wileman, Thomas [1 ,6 ]
机构
[1] Inst Anim Hlth, Pirbright Lab, Surrey, England
[2] Australian Anim Hlth Lab, Geelong, Vic 3219, Australia
[3] Albert Einstein Coll Med, Dept Anat & Struct Biol, Bronx, NY 10467 USA
[4] Univ Autonoma Madrid, Ctr Biol Mol Severo Ochoa, Consejo Super Invest Cient, E-28049 Madrid, Spain
[5] Inst Nacl Salud Carlos III, Ctr Nacl Microbiol, Madrid 28220, Spain
[6] Univ E Anglia, Norwich Med Sch, Norwich NR4 7TJ, Norfolk, England
关键词
African swine fever virus; cisternal collapse; endoplasmic reticulum; viral envelope protein; MAJOR CAPSID PROTEIN; VACCINIA VIRUS; MEMBRANE REARRANGEMENTS; STRUCTURAL PROTEIN; AGGRESOMES; PRECURSORS; EXPRESSION; PP220; SITES; A10L;
D O I
10.1111/j.1600-0854.2011.01293.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Infection of cells with African swine fever virus (ASFV) can lead to the formation of zipper-like stacks of structural proteins attached to collapsed endoplasmic reticulum (ER) cisternae. We show that the collapse of ER cisternae observed during ASFV infection is dependent on the viral envelope protein, J13Lp. Expression of J13Lp alone in cells is sufficient to induce collapsed ER cisternae. Collapse was dependent on a cysteine residue in the N-terminal domain of J13Lp exposed to the ER lumen. Luminal collapse was also dependent on the expression of J13Lp within stacks of ER where antiparallel interactions between the cytoplasmic domains of J13Lp orientated N-terminal domains across ER cisternae. Cisternal collapse was then driven by disulphide bonds between N-terminal domains arranged in antiparallel arrays across the ER lumen. This provides a novel mechanism for biogenesis of modified stacks of ER present in cells infected with ASFV, and may also be relevant to cellular processes.
引用
收藏
页码:30 / 42
页数:13
相关论文
共 30 条
[1]   Cubic membranes:: a legend beyond the Flatland of cell membrane organization [J].
Almsherqi, Zakaria A. ;
Kohlwein, Sepp D. ;
Deng, Yuru .
JOURNAL OF CELL BIOLOGY, 2006, 173 (06) :839-844
[2]   African swine fever virus polyproteins pp220 and pp62 assemble into the core shell [J].
Andrés, G ;
Alejo, A ;
Salas, J ;
Salas, ML .
JOURNAL OF VIROLOGY, 2002, 76 (24) :12473-12482
[3]  
Andrés G, 1998, J VIROL, V72, P8988
[4]   Membrane Rupture Generates Single Open Membrane Sheets during Vaccinia Virus Assembly [J].
Chlanda, Petr ;
Carbajal, Maria Alejandra ;
Cyrklaff, Marek ;
Griffiths, Gareth ;
Krijnse-Locker, Jacomine .
CELL HOST & MICROBE, 2009, 6 (01) :81-90
[5]   Involvement of the endoplasmic reticulum in the assembly and envelopment of African swine fever virus [J].
Cobbold, C ;
Whittle, JT ;
Wileman, T .
JOURNAL OF VIROLOGY, 1996, 70 (12) :8382-8390
[6]   The major structural protein of African swine fever virus, p73, is packaged into large structures, indicative of viral capsid or matrix precursors, on the endoplasmic reticulum [J].
Cobbold, C ;
Wileman, T .
JOURNAL OF VIROLOGY, 1998, 72 (06) :5215-5223
[7]   A virally encoded chaperone specialized for folding of the major capsid protein of African swine fever virus [J].
Cobbold, C ;
Windsor, M ;
Wileman, T .
JOURNAL OF VIROLOGY, 2001, 75 (16) :7221-7229
[8]   Origins of membrane vesicles generated during replication of positive-strand RNA viruses [J].
Cottam, Eleanor ;
Pierini, Roberto ;
Roberts, Rebecca ;
Wileman, Thomas .
FUTURE VIROLOGY, 2009, 4 (05) :473-485
[9]   Pathological and microbiological findings from incidents of unusual mortality of the common frog (Rana temporaria) [J].
Cunningham, AA ;
Langton, TES ;
Bennett, PM ;
Lewin, JF ;
Drury, SEN ;
Gough, RE ;
MacGregor, SK .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1996, 351 (1347) :1539-1557
[10]   VACCINIA AS A MODEL FOR MEMBRANE BIOGENESIS [J].
DALES, S ;
MOSBACH, EH .
VIROLOGY, 1968, 35 (04) :564-&