Marek's disease virus undergoes complete morphogenesis after reactivation in a T-lymphoblastoid cell line transformed by recombinant fluorescent marker virus

被引:13
作者
Denesvre, Caroline [1 ]
Remy, Sylvie [1 ]
Trapp-Fragnet, Laetitia [1 ]
Smith, Lorraine P. [2 ]
Georgeault, Sonia [3 ]
Vautherot, Jean-Francois [1 ]
Nair, Venugopal [2 ]
机构
[1] INRA UMR1282 Infect Dis & Publ Hlth, ISP, BIOVA Team, F-37380 Nouzilly, France
[2] Pirbright Inst, Avian Oncogen Virus Grp, Guildford GU24 0NF, Surrey, England
[3] Univ Tours, Dept Microscopies Plateau Technol Anal Syst Biol, Tours, France
基金
英国生物技术与生命科学研究理事会;
关键词
SCANNING ELECTRON-MICROSCOPY; NUCLEAR EGRESS; IN-VIVO; HERPESVIRUS; TUMOR; MDV; LYMPHOCYTES; TRANSMISSION; EXPRESSION; CHICKENS;
D O I
10.1099/jgv.0.000354
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
T-lymphocytes are central targets of Marek's disease, a major chicken disease induced by the oncogenic alphaherpesvirus Marek's disease virus (MDV). T-lymphocyte infection is also associated with immunosuppression and virus latency. To decipher viral morphogenesis in T-lymphocytes, we used the recombinant vRB-1B 47EGFP marker virus to generate a new lymphoblastoid cell line, 3867K, that exhibited typical properties of other MDV-transformed chicken cell lines in term of cell markers, reactivation rate and infectivity. Examination of reactivating EGFP-positive 3867K cells by transmission electron microscopy revealed the presence of most types of herpesvirus particles inside the cells but no extracellular ones. Quantification of virion types indicated only 5 % cytoplasmic particles, with 0.5 % being mature. This study demonstrated that MDV morphogenesis is complete upon reactivation in T-lymphocytes, albeit with poor efficiency, with a defect in the exit of virions from the nucleus and secondary envelopment, as occurs in infected fibroblasts.
引用
收藏
页码:480 / 486
页数:7
相关论文
共 29 条
[1]  
AKIYAMA Y, 1974, BIKEN J, V17, P105
[2]  
AKIYAMA Y, 1974, BIKEN J, V17, P193
[3]   A full UL13 open reading frame in Marek's disease virus (MDV) is dispensable for tumor formation and feather follicle tropism and cannot restore horizontal virus transmission of rRB-1B in vivo [J].
Blondeau, Caroline ;
Chbab, Najet ;
Beaumont, Catherine ;
Courvoisier, Katia ;
Osterrieder, Nikolaus ;
Vautherot, Jean-Francois ;
Denesvre, Caroline .
VETERINARY RESEARCH, 2007, 38 (03) :419-433
[4]  
Calnek BW, 2001, CURR TOP MICROBIOL, V255, P25
[5]   Morphogenesis of a highly replicative EGFPVP22 recombinant Marek's disease virus in cell culture [J].
Denesvre, C. ;
Blondeau, C. ;
Lemesle, M. ;
Le Vern, Y. ;
Vautherot, D. ;
Roingeard, P. ;
Vautherot, J. F. .
JOURNAL OF VIROLOGY, 2007, 81 (22) :12348-12359
[6]   Marek's Disease Virus Morphogenesis [J].
Denesvre, Caroline .
AVIAN DISEASES, 2013, 57 (02) :340-350
[7]   Keep it in the subfamily: the conserved alphaherpesvirus US3 protein kinase [J].
Deruelle, M. J. ;
Favoreel, H. W. .
JOURNAL OF GENERAL VIROLOGY, 2011, 92 :18-30
[8]  
Dienglewicz RL, 1999, ACTA VIROL, V43, P106
[9]   ULTRASTRUCTURE OF LYMPHOBLASTOID CELL LINES FROM MAREKS-DISEASE LYMPHOMATA [J].
FRAZIER, JA ;
POWELL, PC .
BRITISH JOURNAL OF CANCER, 1975, 31 (01) :7-14
[10]   Fluorescently Tagged pUL47 of Marek's Disease Virus Reveals Differential Tissue Expression of the Tegument Protein In Vivo [J].
Jarosinski, Keith W. ;
Arndt, Sina ;
Kaufer, Benedikt B. ;
Osterrieder, Nikolaus .
JOURNAL OF VIROLOGY, 2012, 86 (05) :2428-2436