Attenuation of Marek's disease virus by codon pair deoptimization of a core gene

被引:12
作者
Conrad, Steven J. [1 ]
Silva, Robert F. [1 ]
Hearn, Carl J. [1 ,2 ]
Climans, Megan [2 ]
Dunn, John R. [1 ]
机构
[1] ARS, Avian Dis & Oncol Lab, USDA, 4279 East Mt Hope Rd, E Lansing, MI 48823 USA
[2] Michigan State Univ, Coll Vet Med, E Lansing, MI 48824 USA
关键词
Codon pair bias; Codon pair score; Deoptimization; Marek's disease virus; MDV; Synthetic attenuated virus engineering; SAVE; DINUCLEOTIDE BIAS; ESCHERICHIA-COLI; VIRAL FITNESS; VACCINE; TRANSFORMATION; POLYPROTEIN; EXPRESSION; INFECTION; VIRULENCE; EVOLUTION;
D O I
10.1016/j.virol.2018.01.020
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Marek's disease virus (MDV) is an oncogenic alphaherpesvirus of Gallus gallus, the domesticated chicken. Control strategies rely upon vaccination with live attenuated viruses of antigenically similar avian herpesviruses or attenuated strains of MDV. Recent studies in other viruses have shown that recoding certain viral genes to employ synonymous but rarely-used codon pairs resulted in viral attenuation. We deoptimized two MDV proteins, UL54/ICP27 and UL49/VP22, and demonstrate that the more severely deoptimized variant of UL54 accumulates significantly less gene product in vitro. Using these UL54 deoptimized mutants, we further demonstrate that animals infected with the UL54-recoded recombinant virus exhibited decreased viral genome copy number in lymphocytes, reduced lymphoid atrophy and reduced tumor incidence. This study demonstrates that codon pair deoptimization of a single viral gene can produce attenuated strains of MDV. This approach may be useful as a rational way of making novel live attenuated virus vaccines for MDV.
引用
收藏
页码:219 / 226
页数:8
相关论文
共 50 条
[1]   PATHOGENESIS OF MAREKS-DISEASE - EARLY DISTRIBUTION OF VIRUS AND VIRAL ANTIGENS IN INFECTED CHICKENS [J].
ADLDINGE.HK ;
CALNEK, BW .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1973, 50 (05) :1287-1298
[2]   ICP27 protein of Marek's disease virus interacts with SR proteins and inhibits the splicing of cellular telomerase chTERT and viral vIL8 transcripts [J].
Amor, S. ;
Strassheim, S. ;
Dambrine, G. ;
Remy, S. ;
Rasschaert, D. ;
Laurent, S. .
JOURNAL OF GENERAL VIROLOGY, 2011, 92 :1273-1278
[3]   Synonymous Virus Genome Recocing as a Tool to Impact Viral Fitness [J].
Angel Martinez, Miguel ;
Jordan-Paiz, Ana ;
Franco, Sandra ;
Nevot, Maria .
TRENDS IN MICROBIOLOGY, 2016, 24 (02) :134-147
[4]  
[Anonymous], PLOS ONE
[5]  
Baker S., 2015, FUTURE VIROL, V10, P1
[6]  
BENNETZEN JL, 1982, J BIOL CHEM, V257, P3026
[7]  
Biggs P M, 1975, Br J Cancer Suppl, V2, P152
[8]  
BIGGS PM, 1968, PERSPECT VIROL, V6, P211
[9]   Functional homologies between avian and human alphaherpesvirus VP22 proteins in cell-to-cell spreading as revealed by a new cis-complementation assay [J].
Blondeau, C. ;
Marc, D. ;
Courvoisier, K. ;
Vautherot, J. -F. ;
Denesvre, C. .
JOURNAL OF VIROLOGY, 2008, 82 (18) :9278-9282
[10]   The Effects of Codon Context on In Vivo Translation Speed [J].
Chevance, Fabienne F. V. ;
Le Guyon, Soazig ;
Hughes, Kelly T. .
PLOS GENETICS, 2014, 10 (06)