Replication kinetics of different porcine circovirus 2 strains in PK-15 cells, fetal cardiomyocytes and macrophages

被引:79
作者
Meerts, P
Misinzo, G
McNeilly, F
Nauwynck, HJ
机构
[1] Univ Ghent, Fac Vet Med, Virol Lab, B-9820 Merelbeke, Belgium
[2] Dept Agr & Rural Dev No Ireland, Vet Sci Div, Belfast, Antrim, North Ireland
关键词
D O I
10.1007/s00705-004-0444-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In this in vitro study, the replication kinetics of porcine circovirus type 2 (PCV2) in porcine alveolar macrophages (PAM) and fetal cardiomyocytes (FCM), two target cells in vivo, was compared with that in PK-15 cells. Cultures were inoculated with either the postweaning multisystemic wasting syndrome (PMWS)-associated strain Stoon-1010 or the abortion-associated strain 1121. Viral proteins were visualized and virus production was determined. In PK-15 cells, the capsid protein was expressed between 6 and 12 hours post inoculation (hpi), it relocated to the nucleus between 12 and 24 hpi. At that time, Rep protein was also detected in the nucleus. This sequence of events also occurred in FCM and PAM but nuclear localized antigens appeared later (48 hpi) and in a lower percentage of cells. In PAM, clear differences in susceptibility were seen between pigs. In PAM from two out of five tested pigs, nuclear localized antigens were not detected, whereas in PAM from three other pigs they were seen in up to 20% of the antigen-positive cells. Virus production was observed in PK-15 but not in PAM or FCM cultures. In a second study, the replication kinetics of seven different PCV2 strains were compared in PK-15 cells. It was shown that the two abortion-associated strains had a different replication kinetics in comparison with PMWS or porcine dermatitis and nephropathy syndrome associated strains. With the abortion-associated strains, a higher number of infected cells was observed at 24 hpi and the percentage of infected cells with nuclear localised antigens was lower compared to that of other strains.
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页码:427 / 441
页数:15
相关论文
共 32 条
[21]   PORCINE RESPIRATORY CORONAVIRUS DIFFERS FROM TRANSMISSIBLE GASTROENTERITIS VIRUS BY A FEW GENOMIC DELETIONS [J].
RASSCHAERT, D ;
DUARTE, M ;
LAUDE, H .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :2599-2607
[22]   Characteristics of porcine circovirus-2 replication in lymphoid organs of pigs inoculated in late gestation or postnatally and possible relation to clinical and pathological outcome of infection [J].
Sanchez, RE ;
Meerts, P ;
Nauwynck, HJ ;
Ellis, JA ;
Pensaert, MB .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2004, 16 (03) :175-185
[23]   Change of porcine circovirus 2 target cells in pigs during development from fetal to early postnatal life [J].
Sanchez, RE ;
Meerts, P ;
Nauwynck, HJ ;
Pensaert, MB .
VETERINARY MICROBIOLOGY, 2003, 95 (1-2) :15-25
[24]   Porcine circovirus 2 infection in swine foetuses inoculated at different stages of gestation [J].
Sanchez, RE ;
Nauwynck, HJ ;
McNeilly, F ;
Allan, GM ;
Pensaert, MB .
VETERINARY MICROBIOLOGY, 2001, 83 (02) :169-176
[25]   Rep and Rep′ protein of Porcine circovirus type 1 bind to the origin of replication in vitro [J].
Steinfeldt, T ;
Finsterbusch, T ;
Mankertz, A .
VIROLOGY, 2001, 291 (01) :152-160
[26]  
TISCHER I, 1988, ZBL BAKT-INT J MED M, V270, P280
[27]   REPLICATION OF PORCINE CIRCOVIRUS - INDUCTION BY GLUCOSAMINE AND CELL-CYCLE DEPENDENCE [J].
TISCHER, I ;
PETERS, D ;
RASCH, R ;
POCIULI, S .
ARCHIVES OF VIROLOGY, 1987, 96 (1-2) :39-57
[28]   STUDIES ON EPIDEMIOLOGY AND PATHOGENICITY OF PORCINE CIRCOVIRUS [J].
TISCHER, I ;
MIELDS, W ;
WOLFF, D ;
VAGT, M ;
GRIEM, W .
ARCHIVES OF VIROLOGY, 1986, 91 (3-4) :271-276
[29]   A VERY SMALL PORCINE VIRUS WITH CIRCULAR SINGLE-STRANDED-DNA [J].
TISCHER, I ;
GELDERBLOM, H ;
VETTERMANN, W ;
KOCH, MA .
NATURE, 1982, 295 (5844) :64-66
[30]   Involvement of sialoadhesin in entry of porcine reproductive and respiratory syndrome virus into porcine alveolar macrophages [J].
Vanderheijden, N ;
Delputte, PL ;
Favoreel, HW ;
Vandekerckhove, J ;
Van Damme, J ;
van Woensel, PA ;
Nauwynck, HJ .
JOURNAL OF VIROLOGY, 2003, 77 (15) :8207-8215