Mutations in the spike gene of porcine epidemic diarrhea virus associated with growth adaptation in vitro and attenuation of virulence in vivo

被引:133
作者
Sato, Tetsuo [1 ]
Takeyama, Natsumi [1 ]
Katsumata, Atsushi [1 ]
Tuchiya, Kotaro [1 ]
Kodama, Toshiaki [1 ]
Kusanagi, Ko-ichi [1 ]
机构
[1] Nippon Inst Biol Sci, Tokyo 1980024, Japan
关键词
Growth adaptation; Mutation; Porcine epidemic diarrhea virus; Serial passage; Spike gene; Virus attenuation; TRANSMISSIBLE GASTROENTERITIS VIRUS; INFECTIOUS-BRONCHITIS VIRUS; CORONAVIRUS ENVELOPE; PROTEIN GENES; SEQUENCE; PATHOGENICITY; STRAINS; IDENTIFICATION; GLYCOPROTEIN; DETERMINANT;
D O I
10.1007/s11262-011-0617-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Previously, we have reported that a serial passage of 83P-5 strain of porcine epidemic diarrhea virus (PEDV) in Vero cells resulted in a growth adaptation of the virus in cultured cells at the 22nd passage. In this study, we further maintained the 83P-5 in Vero cells up to the 100th passage and analyzed changes in the spike (S), membrane (M), and nucleocapsid (N) gene sequences and pathogenicity of the virus at the 34th, 61st, and 100th passage levels. Sequence analyses revealed a strong selection for the S gene of 83P-5 in Vero cells, and virtually all mutations occurring at the 34th and 61st passages had been carried over to the 100th-passaged virus. In contrast, the viral M and N genes showed a strong conservation during the serial passage. Pigs experimentally infected with the 34th- or 61st-passaged virus, but not the 100th-passaged virus, exhibited diarrhea, indicating an attenuation of the 83P-5 at the 100th passage. Interestingly, S protein of the attenuated 100th-passaged 83P-5 showed a remarkable sequence similarity to that of previously reported DR-13 strain of attenuated PEDV that also had been established by serial passage in Vero cells. Further studies will be required to define whether the mutations in the S gene of 83P-5 that had been selected and accumulated during the serial passages are indeed the causalities of the growth adaptation in vitro and the attenuation of virulence in vivo.
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页码:72 / 78
页数:7
相关论文
共 39 条
[1]   Identification of sequence changes responsible for the attenuation of avian infectious bronchitis virus strain Arkansas DPI [J].
Ammayappan, Arun ;
Upadhyay, Chitra ;
Gelb, Jack, Jr. ;
Vakharia, Vikram N. .
ARCHIVES OF VIROLOGY, 2009, 154 (03) :495-499
[2]   The Replicase Gene of Avian Coronavirus Infectious Bronchitis Virus Is a Determinant of Pathogenicity [J].
Armesto, Maria ;
Cavanagh, Dave ;
Britton, Paul .
PLOS ONE, 2009, 4 (10)
[3]   SITE-SPECIFIC ALTERATION OF TRANSMISSIBLE GASTROENTERITIS VIRUS SPIKE PROTEIN RESULTS IN MARKEDLY REDUCED PATHOGENICITY [J].
BERNARD, S ;
LAUDE, H .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :2235-2241
[4]   Prevalence of porcine epidemic diarrhoea virus and transmissible gastroenteritis virus infection in Korean pigs [J].
Chae, C ;
Kim, O ;
Choi, C ;
Min, K ;
Cho, WS ;
Kim, J ;
Tai, JH .
VETERINARY RECORD, 2000, 147 (21) :606-608
[5]   The GPRLQPY motif located at the carboxy-terminal of the spike protein induces antibodies that neutralize Porcine epidemic diarrhea virus [J].
Cruz, Deu John M. ;
Kim, Chul-Joong ;
Shin, Hyun-Jin .
VIRUS RESEARCH, 2008, 132 (1-2) :192-196
[6]   Assembly of the coronavirus envelope: Homotypic interactions between the M proteins [J].
de Haan, CAM ;
Vennema, H ;
Rottier, PJM .
JOURNAL OF VIROLOGY, 2000, 74 (11) :4967-4978
[7]   The group-specific murine coronavirus genes are not essential, but their deletion, by reverse genetics, is attenuating in the natural host [J].
de Haan, CAM ;
Masters, PS ;
Shen, XL ;
Weiss, S ;
Rottier, PJM .
VIROLOGY, 2002, 296 (01) :177-189
[8]   Mapping of the coronavirus membrane protein domains involved in interaction with the spike protein [J].
de Haan, CAM ;
Smeets, M ;
Vernooij, F ;
Vennema, H ;
Rottier, PJM .
JOURNAL OF VIROLOGY, 1999, 73 (09) :7441-7452
[9]  
DEBOUCK P, 1980, AM J VET RES, V41, P219
[10]  
DUCATELLE R, 1981, ZBL VET MED B, V28, P483