Hosting the severe acute respiratory syndrome coronavirus: specific cell factors required for infection

被引:18
作者
de Haan, Cornelis A. M. [1 ]
Rottier, Peter J. M. [1 ]
机构
[1] Univ Utrecht, Fac Vet Med, Dept Immunol & Infect Dis, Div Virol, NL-3584 CL Utrecht, Netherlands
关键词
D O I
10.1111/j.1462-5822.2006.00744.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
As with all viruses, the severe acute respiratory syndrome coronavirus (SARS-CoV) utilizes specific host cell factors during its infection cycle. Some of these factors have been identified and are now increasingly scrutinized as targets to intervene with infection. In this brief review, we describe the current understanding of how the SARS-CoV is able to use the cellular machinery for its replication.
引用
收藏
页码:1211 / 1218
页数:8
相关论文
共 74 条
  • [1] The nucleoprotein is required for efficient coronavirus genome replication
    Almazán, F
    Galán, C
    Enjuanes, L
    [J]. JOURNAL OF VIROLOGY, 2004, 78 (22) : 12683 - 12688
  • [2] Amino acids 270 to 510 of the severe acute respiratory syndrome coronavirus spike protein are required for interaction with receptor
    Babcock, GJ
    Esshaki, DJ
    Thomas, WD
    Ambrosino, DM
    [J]. JOURNAL OF VIROLOGY, 2004, 78 (09) : 4552 - 4560
  • [3] Severe acute respiratory syndrome coronavirus spike protein expressed by attenuated vaccinia virus protectively immunizes mice
    Bisht, H
    Roberts, A
    Vogel, L
    Bukreyev, A
    Collins, PL
    Murphy, BR
    Subbarao, K
    Moss, B
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (17) : 6641 - 6646
  • [4] Severe acute respiratory syndrome coroavirus (SARS-CoV) infection inhibition using spike protein heptad repeat-derived peptides
    Bosch, BJ
    Martina, BEE
    van der Zee, R
    Lepault, J
    Haijema, BJ
    Versluis, C
    Heck, AJR
    de Groot, R
    Osterhaus, ADME
    Rottier, PJM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (22) : 8455 - 8460
  • [5] The coronavirus spike protein is a class I virus fusion protein: Structural and functional characterization of the fusion core complex
    Bosch, BJ
    van der Zee, R
    de Haan, CAM
    Rottier, PJM
    [J]. JOURNAL OF VIROLOGY, 2003, 77 (16) : 8801 - 8811
  • [6] Mouse hepatitis virus replicase protein complexes are translocated to sites of M protein accumulation in the ERGIC at late times of infection
    Bost, AG
    Prentice, E
    Denison, MR
    [J]. VIROLOGY, 2001, 285 (01) : 21 - 29
  • [7] Homozygous L-SIGN (CLEC4M) plays a protective role in SARS coronavirus infection
    Chan, VSF
    Chan, KYK
    Chen, YX
    Poon, LLM
    Cheung, ANY
    Zheng, BJ
    Chan, KH
    Mak, W
    Ngan, HYS
    Xu, XN
    Screaton, G
    Tam, PKH
    Austyn, JM
    Chan, LC
    Yip, SP
    Peiris, M
    Khoo, US
    Lin, CLS
    [J]. NATURE GENETICS, 2006, 38 (01) : 38 - 46
  • [8] Molecular interactions in the assembly of coronaviruses
    de Haan, CAM
    Rottier, PJM
    [J]. VIRUS STRUCTURE AND ASSEMBLY, 2005, 64 : 165 - 230
  • [9] Cleavage inhibition of the murine coronavirus spike protein by a furin-like enzyme affects cell-cell but not virus-cell fusion
    de Haan, CAM
    Stadler, K
    Godeke, GJ
    Bosch, BJ
    Rottier, PJM
    [J]. JOURNAL OF VIROLOGY, 2004, 78 (11) : 6048 - 6054
  • [10] Identification of a novel coronavirus in patients with severe acute respiratory syndrome
    Drosten, C
    Günther, S
    Preiser, W
    van der Werf, S
    Brodt, HR
    Becker, S
    Rabenau, H
    Panning, M
    Kolesnikova, L
    Fouchier, RAM
    Berger, A
    Burguière, AM
    Cinatl, J
    Eickmann, M
    Escriou, N
    Grywna, K
    Kramme, S
    Manuguerra, JC
    Müller, S
    Rickerts, V
    Stürmer, M
    Vieth, S
    Klenk, HD
    Osterhaus, ADME
    Schmitz, H
    Doerr, HW
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (20) : 1967 - 1976