Proliferative growth of SARS coronavirus in Vero E6 cells

被引:89
作者
Ng, ML
Tan, SH
See, EE
Oi, EE
Ling, AE
机构
[1] Natl Univ Singapore, Dept Microbiol, Singapore 117597, Singapore
[2] Natl Univ Singapore, Fac Med, Electron Microscopy Unit, Singapore 117597, Singapore
[3] Natl Environm Agcy, Environm Hlth Inst, Singapore, Singapore
[4] Singapore Gen Hosp, Dept Pathol, Singapore, Singapore
关键词
D O I
10.1099/vir.0.19505-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
An isolate of SARS coronavirus (strain 2003VA2774) was obtained from a patient and used to infect Vero E6 cells. The replication cycle of the virus was followed from 1 to 30 h post-infection (p.i.). It was surprising to observe the swift growth of this human virus in Vero cells. Within the first hour of infection, the most obvious ultrastructural change was the proliferation of the Golgi complexes and related vesicles accompanied by swelling of some of the trans-Golgi sacs. Extracellular virus particles were present by 5 h p.i. in about 5% of the cells and this increased dramatically to about 30% of the cell population within an hour (6 h p.i.). Swollen Golgi sacs contained virus nucleocapsids at different stages of maturation. These virus precursors were also in large vacuoles and in close association with membrane whorls. The membrane whorls could be the replication complexes, since they appeared rather early in the replication cycle. As infection progressed from 12 to 21 h p.i., the cytoplasm of the infected cells was filled with numerous large, smooth-membraned vacuoles containing a mixture of mature virus and spherical cores. Several of these vacuoles were close to the cell periphery, ready to export out the mature progeny virus particles via exocytosis. By 24 to 30 h p.i., crystalline arrays of the extracellular virus particles were seen commonly at the cell surface.
引用
收藏
页码:3291 / 3303
页数:13
相关论文
共 29 条
[1]   ESTABLISHMENT AND MAINTENANCE OF A PERSISTENT INFECTION OF L132 CELLS BY HUMAN CORONAVIRUS STRAIN 229E [J].
CHALONERLARSSON, G ;
JOHNSONLUSSENBURG, CM .
ARCHIVES OF VIROLOGY, 1981, 69 (02) :117-129
[2]   AN ELECTRON MICROSCOPE STUDY OF DEVELOPMENT OF A MOUSE HEPATITIS VIRUS IN TISSUE CULTURE CELLS [J].
DAVIDFERREIRA, JF ;
MANAKER, RA .
JOURNAL OF CELL BIOLOGY, 1965, 24 (01) :57-+
[3]   Identification of a novel coronavirus in patients with severe acute respiratory syndrome [J].
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 .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (20) :1967-1976
[4]  
Fleming J O, 1987, Adv Exp Med Biol, V218, P333
[5]   ANTIGENIC ASSESSMENT OF CORONAVIRUSES ISOLATED FROM PATIENTS WITH MULTIPLE-SCLEROSIS [J].
FLEMING, JO ;
ELZAATARI, FAK ;
GILMORE, W ;
BERNE, JD ;
BURKS, JS ;
STOHLMAN, SA ;
TOURTELLOTTE, WW ;
WEINER, LP .
ARCHIVES OF NEUROLOGY, 1988, 45 (06) :629-633
[6]   PROTEOLYTIC CLEAVAGE OF THE E2-GLYCOPROTEIN OF MURINE CORONAVIRUS - HOST-DEPENDENT DIFFERENCES IN PROTEOLYTIC CLEAVAGE AND CELL-FUSION [J].
FRANA, MF ;
BEHNKE, JN ;
STURMAN, LS ;
HOLMES, KV .
JOURNAL OF VIROLOGY, 1985, 56 (03) :912-920
[7]  
Holmes K. V., 1990, VIROLOGY, V1, P841
[8]  
HOLMES KC, 1984, ADV EXP MED BIOL, V170, P373
[9]  
HOLMES KV, 1982, ADV EXP MED BIOL, V142, P287
[10]  
HOLMES KV, 1982, ADV EXP MED BIOL, V142, P133