Feline coronavirus type II strains 79-1683 and 79-1146 originate from a double recombination between feline coronavirus type I and canine coronavirus

被引:334
作者
Herrewegh, AAPM [1 ]
Smeenk, I [1 ]
Horzinek, MC [1 ]
Rottier, PJM [1 ]
de Groot, RJ [1 ]
机构
[1] Univ Utrecht, Dept Immunol & Infect Dis, Virol Unit, Fac Vet Med, NL-3508 TD Utrecht, Netherlands
关键词
D O I
10.1128/JVI.72.5.4508-4514.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Recent evidence suggests that the type II feline coronavirus (FCoV) strains 79-1146 and 79-1683 have arisen from a homologous RNA recombination event between FCoV type I and canine coronavirus (CCV). In both cases, the template switch apparently took place between the S and M genes, giving rise to recombinant viruses which encode a CCV-like S protein and the M, N, 7a, and 7b proteins of FCoV type I (K. Motowaka, T. Hohdatsu, H. Hashimoto, and H. Koyama, Microbiol. Immunol. 40:425-433, 1996; H. Vennema, A. Poland, K. Floyd Hawkins, and N. C. Pedersen, Feline Pract. 23:40-44, 1995). In the present study, we have looked for additional FCoV-CCV recombination sites. Four regions in the pol gene were selected for comparative sequence analysis of the type II FCoV strains 79-1683 and 79-1146, the type I FCoV strains TN406 and UCD1, the CCV strain K378, and the TGEV strain Purdue. Our data show that the type II FCoVs have arisen from double recombination events: additional crossover sites were mapped in the ORF1ab frameshifting region of strain 79-1683 and in the 5' half of ORF1b of strain 79-1146.
引用
收藏
页码:4508 / 4514
页数:7
相关论文
共 50 条
[1]   RANDOM NATURE OF CORONAVIRUS RNA RECOMBINATION IN THE ABSENCE OF SELECTION PRESSURE [J].
BANNER, LR ;
LAI, MMC .
VIROLOGY, 1991, 185 (01) :441-445
[2]   ESTABLISHING A GENETIC-RECOMBINATION MAP FOR MURINE CORONAVIRUS STRAIN A59 COMPLEMENTATION GROUPS [J].
BARIC, RS ;
FU, K ;
SCHAAD, MC ;
STOHLMAN, SA .
VIROLOGY, 1990, 177 (02) :646-656
[3]  
BARLOUGH JE, 1984, LAB ANIM SCI, V34, P592
[4]   CHIMERIC PARVOVIRUS B19 CAPSIDS FOR THE PRESENTATION OF FOREIGN EPITOPES [J].
BROWN, CS ;
WELLINGWESTER, S ;
FEIJLBRIEF, M ;
VANLENT, JWM ;
SPAAN, WJM .
VIROLOGY, 1994, 198 (02) :477-488
[5]   CORONAVIRUS IBV - VIRUS RETAINING SPIKE GLYCOPOLYPEPTIDE-S2 BUT NOT S1 IS UNABLE TO INDUCE VIRUS-NEUTRALIZING OR HEMAGGLUTINATION-INHIBITING ANTIBODY, OR INDUCE CHICKEN TRACHEAL PROTECTION [J].
CAVANAGH, D ;
DAVIS, PJ ;
DARBYSHIRE, JH ;
PETERS, RW .
JOURNAL OF GENERAL VIROLOGY, 1986, 67 :1435-1442
[6]   FITNESS OF RNA VIRUS DECREASED BY MULLER RATCHET [J].
CHAO, L .
NATURE, 1990, 348 (6300) :454-455
[7]   NATURE OF POLIOVIRUS GENETIC RECOMBINANTS [J].
COOPER, PD ;
STEINERP.A ;
SCOTTI, PD ;
DELONG, D .
JOURNAL OF GENERAL VIROLOGY, 1974, 23 (APR) :41-49
[8]   The genome organization of the nidovirales: Similarities and differences between arteri-, toro-, and coronaviruses [J].
de Vries, AAF ;
Horzinek, MC ;
Rottier, PJM ;
de Groot, RJ .
SEMINARS IN VIROLOGY, 1997, 8 (01) :33-47
[9]   INTRACELLULAR RNAS OF THE FELINE INFECTIOUS PERITONITIS CORONAVIRUS STRAIN 79-1146 [J].
DEGROOT, RJ ;
TERHAAR, RJ ;
HORZINEK, MC ;
VANDERZEIJST, BAM .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :995-1002
[10]   COMPLETE SEQUENCE (20 KILOBASES) OF THE POLYPROTEIN-ENCODING GENE-1 OF TRANSMISSIBLE GASTROENTERITIS VIRUS [J].
ELEOUET, JF ;
RASSCHAERT, D ;
LAMBERT, P ;
LEVY, L ;
VENDE, P ;
LAUDE, H .
VIROLOGY, 1995, 206 (02) :817-822