Genetic characterization of equine arteritis virus during persistent infection of stallions

被引:41
作者
Balasuriya, UBR [1 ]
Hedges, JF
Smalley, VL
Navarrette, A
McCollum, WH
Timoney, PJ
Snijder, EJ
MacLachlan, NJ
机构
[1] Univ Calif Davis, Sch Vet Med, Dept Pathol Microbiol & Immunol, Bernard & Gloria Salick Equine Viral Dis Lab, Davis, CA 95616 USA
[2] Univ Kentucky, Dept Vet Sci, Gluck Equine Res Ctr, Lexington, KY 40546 USA
[3] Leiden Univ, Ctr Med, Dept Med Microbiol, Mol Virol Lab, NL-2300 RC Leiden, Netherlands
关键词
D O I
10.1099/vir.0.19545-0
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
Equine arteritis virus (EAV) causes a persistent infection of the reproductive tract of carrier stallions. The authors determined the complete genome sequences of viruses (CW96 and CW01) that were present 5 years apart in the semen of a carrier stallion (CW). The CW96 and CW01 viruses respectively had only 85(.)6% and 85(.)7% nucleotide identity to the published sequence of EAV (EAV030). The CW96 and CW01 viruses had two 1 nt insertions and a single 1 nt deletion in the leader sequence, and a 3 nt coding insertion in ORF1a; thus their genomes included 12 708 nt as compared to the 12 704 nt in EAV030. Variation between viruses present in the semen of stallion CW and EAV030 was especially marked in the replicase gene (ORF1 a and 1b), and the greatest variation occurred in the portion of ORF1a encoding the nsp2 protein. The ORFs 3 and 5, which respectively encode the GP3 and GP5 envelope proteins, showed greatest variation amongst ORFs encoding structural EAV proteins. Comparative sequence analyses of CW96 and CW01 indicated that ORFs 1a, 1b and 7 were highly conserved during persistent infection, whereas there was substantial variation in ORFs 3 and 5. Although the variation that occurs in ORF5 results in the emergence of novel phenotypic viral variants as determined by neutralization assay, all variants were neutralized by high-titre polyclonal equine antisera, suggesting that immune evasion is unlikely to be responsible for the establishment of persistent EAV infection of carrier stallions. Northern blot analyses of RNA extracted from cell culture propagated viruses isolated from 10 different persistently infected stallions failed to demonstrate any large genomic deletions, suggesting that defective interfering particles are also unlikely to be important in either the maintenance or clearance of persistent EAV infection of the reproductive tract of carrier stallions.
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页码:379 / 390
页数:12
相关论文
共 55 条
[1]   IDENTIFICATION OF A NEUTRALIZATION SITE IN THE MAJOR ENVELOPE GLYCOPROTEIN (G(L)) OF EQUINE ARTERITIS VIRUS [J].
BALASURIYA, UBR ;
MACLACHLAN, NJ ;
DEVRIES, AAF ;
ROSSITTO, PV ;
ROTTIER, PJM .
VIROLOGY, 1995, 207 (02) :518-527
[2]   A 29K ENVELOPE GLYCOPROTEIN OF EQUINE ARTERITIS VIRUS EXPRESSES NEUTRALIZATION DETERMINANTS RECOGNIZED BY MURINE MONOCLONAL-ANTIBODIES [J].
BALASURIYA, UBR ;
ROSSITTO, PV ;
DEMAULA, CD ;
MACLACHLAN, NJ .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :2525-2529
[3]   Neutralization determinants of laboratory strains and field isolates of equine arteritis virus: Identification of four neutralization sites in the amino-terminal ectodomain of the G(L) envelope glycoprotein [J].
Balasuriya, UBR ;
Patton, JF ;
Rossitto, PV ;
Timoney, PJ ;
McCollum, WH ;
MacLachlan, NJ .
VIROLOGY, 1997, 232 (01) :114-128
[4]  
Balasuriya UBR, 2001, ADV EXP MED BIOL, V494, P19
[5]   Alphavirus replicon particles expressing the two major envelope proteins of equine arteritis virus induce high level protection against challenge with virulent virus in vaccinated horses [J].
Balasuriya, UBR ;
Heidner, HW ;
Davis, NL ;
Wagner, HM ;
Hullinger, PJ ;
Hedges, JF ;
Williams, JC ;
Johnston, RE ;
Wilson, WD ;
Liu, IK ;
MacLachlan, NJ .
VACCINE, 2002, 20 (11-12) :1609-1617
[6]   Genetic stability of equine arteritis virus during horizontal and vertical transmission in an outbreak of equine viral arteritis [J].
Balasuriya, UBR ;
Hedges, JF ;
Nadler, SA ;
McCollum, WH ;
Timoney, PJ ;
MacLachlan, NJ .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :1949-1958
[7]  
Balasuriya UBR, 1998, J AM VET MED ASSOC, V213, P1586
[8]   Phylogenetic analysis of open reading frame 5 of field isolates of equine arteritis virus and identification of conserved and nonconserved regions in the G(L) envelope glycoprotein [J].
Balasuriya, UBR ;
Timoney, PJ ;
McCollum, WH ;
MacLachlan, NJ .
VIROLOGY, 1995, 214 (02) :690-697
[9]   Expression of the two major envelope proteins of equine arteritis virus as a heterodimer is necessary for induction of neutralizing antibodies in mice immunized with recombinant venezuelan equine encephalitis virus replicon particles [J].
Balasuriya, UBR ;
Heidner, HW ;
Hedges, JF ;
Williams, JC ;
Davis, NL ;
Johnston, RE ;
MacLachlan, NJ .
JOURNAL OF VIROLOGY, 2000, 74 (22) :10623-10630
[10]  
Cavanagh D, 1997, ARCH VIROL, V142, P629