A functional link between the actin cytoskeleton and lipid rafts during budding of filamentous influenza virions

被引:105
作者
Simpson-Holley, M
Ellis, D
Fisher, D
Elton, D
McCauley, J
Digard, P
机构
[1] Univ Cambridge, Dept Pathol, Div Virol, Cambridge CB2 1QP, England
[2] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1QJ, England
[3] AFRC, Inst Anim Hlth, Newbury RG20 7NN, Berks, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
cytochalasin D; latrunculin A; atomic force microscopy;
D O I
10.1006/viro.2002.1595
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Morphogenesis of influenza virus is a poorly understood process that produces two types of enveloped virion: similar to 100-nm spheres and similar diameter filaments that reach 20 mum in length. Spherical particles assemble at plasma membrane lipid rafts in a process independent of microfilaments, The budding site of filamentous virions is hitherto uncharacterised but their formation involves the actin cytoskeleton. We confirm microfilament involvement in filamentous budding and show that after disruption of cortical actin by jasplakinolide, HA, NP, and M1 redistributed around beta-actin clusters to form novel annular membrane structures. HA in filamentous virions and jasplakinolide-induced annuli was detergent insoluble at 4degreesC. Furthermore, in both cases HA partitioned into low buoyant density detergent-insoluble glycolipid domains, indicating that filamentous virions and annuli contain reorganised lipid rafts, We propose that the actin cytoskeleton is required to maintain the correct organisation of lipid rafts for incorporation into budding viral filaments. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:212 / 225
页数:14
相关论文
共 68 条
  • [1] Influenza virus assembly: Effect of influenza virus glycoproteins on the membrane association of M1 protein
    Ali, A
    Avalos, RT
    Ponimaskin, E
    Nayak, DP
    [J]. JOURNAL OF VIROLOGY, 2000, 74 (18) : 8709 - 8719
  • [2] Association of influenza virus NP and M1 proteins with cellular cytoskeletal elements in influenza virus-infected cells
    Avalos, RT
    Yu, Z
    Nayak, DP
    [J]. JOURNAL OF VIROLOGY, 1997, 71 (04) : 2947 - 2958
  • [3] BACHI T, 1969, J VIROL, V4, P769
  • [4] Analysis of the transmembrane domain of influenza virus neuraminidase, a type II transmembrane glycoprotein, for apical sorting and raft association
    Barman, S
    Nayak, DP
    [J]. JOURNAL OF VIROLOGY, 2000, 74 (14) : 6538 - 6545
  • [5] Acyl and alkyl chain length of GPI-anchors is critical for raft association in vitro
    Benting, J
    Rietveld, A
    Ansorge, I
    Simons, K
    [J]. FEBS LETTERS, 1999, 462 (1-2) : 47 - 50
  • [6] Inhibition of the influenza virus RNA-dependent RNA polymerase by antisera directed against the carboxy-terminal region of the PB2 subunit
    Blok, V
    Cianci, C
    Tibbles, KW
    Inglis, SC
    Krystal, M
    Digard, P
    [J]. JOURNAL OF GENERAL VIROLOGY, 1996, 77 : 1025 - 1033
  • [7] BOHN W, 1987, SCANNING MICROSCOPY, V1, P319
  • [8] Structure and function of sphingolipid- and cholesterol-rich membrane rafts
    Brown, DA
    London, E
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (23) : 17221 - 17224
  • [9] Functions of lipid rafts in biological membranes
    Brown, DA
    London, E
    [J]. ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1998, 14 : 111 - 136
  • [10] SORTING OF GPI-ANCHORED PROTEINS TO GLYCOLIPID-ENRICHED MEMBRANE SUBDOMAINS DURING TRANSPORT TO THE APICAL CELL-SURFACE
    BROWN, DA
    ROSE, JK
    [J]. CELL, 1992, 68 (03) : 533 - 544