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Virologica Sinica logoLink to Virologica Sinica
. 2012 Jan 22;27(1):26–37. doi: 10.1007/s12250-012-3221-5

Molecular and in vitro characterization of field isolates of bovine herpesvirus-1

Julian Ruiz-Saenz 1, Jairo Jaime 1, Gloria Ramirez 1, Victor Vera 1,
PMCID: PMC8218024  PMID: 22270804

Abstract

Bovine Herpesvirus-1 (BoHV-1) is distributed worldwide and is a major pathogen in cattle, being the causal agent of a variety of clinical syndromes. The aim of this study was to isolate and to characterize (molecular and biological characterization) BoHV-1 from 29 immunosuppressed animals. It was possible to obtain 18 isolates, each from a different animal, such as from the respiratory and reproductive tracts. In some cases the cytopathic effect was visible 12 hours post-inoculation, and became characteristic after 36–48 hours. Biological characteristics were evaluated and compared with Iowa and Colorado-1 reference strains, and differences were found in plaque size, virus titer measured by TCID50 and PFU/mL, and one step virus curves. These results showed that some isolates had a highly virulent-like behavior in vitro, compared to the reference strains, with shorter eclipse periods, faster release of virus into the supernatants, and higher burst size and viral titer. There were no differences in glycoprotein expression of BoHV-1 isolates, measured by Western blot on monolayers. Moreover, using restriction endonucleases analysis, most of the viruses were confirmed as BoHV-1.1 and just one of them was confirmed as BoHV-1.2a subtype. These findings suggest that some wild-type BoHV-1 isolates could be useful as seeds to develop new monovalent vaccines.

Key words: Bovine herpesvirus 1, Genital infection, Respiratory infection, Latent infection

Footnotes

Foundation items: the División de Investigación Universidad Nacional de Colombia, grants No. 20201007738 and 202010013254.

References

  • 1.Abril C., Engels M., Liman A., et al. Both viral and host factors contribute to neurovirulence of bovine herpesviruses 1 and 5 in interferon receptor deficient mice. J Virol. 2004;78(7):3644–3653. doi: 10.1128/JVI.78.7.3644-3653.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Büchen-Osmond C. Alphabetical List of ICTV approved Virus Families and Genera. Created April, 1995. Last Modified 08-07-2008.
  • 3.Chowdhury S. I. Construction and characterization of an attenuated bovine herpesvirus type 1 (BHV-1) recombinant virus. Vet Microbiol. 1996;52(1–2):13–23. doi: 10.1016/0378-1135(96)00043-0. [DOI] [PubMed] [Google Scholar]
  • 4.D’Arce R. C., Almeida R. S., Silva T. C., et al. Restriction endonuclease and monoclonal antibody analysis of Brazilian isolates of bovine herpesviruses types 1 and 5. Vet Microbiol. 2002;88:315–324. doi: 10.1016/S0378-1135(02)00126-8. [DOI] [PubMed] [Google Scholar]
  • 5.Dasika G. K., Letchworth G. J., 3rd Cellular expression of bovine herpesvirus 1 gD inhibits cell-to-cell spread of two closely related viruses without blocking their primary infection. Virology. 1999;254(1):24–36. doi: 10.1006/viro.1998.9553. [DOI] [PubMed] [Google Scholar]
  • 6.Dry I., Haig D. M., Inglis N. F., et al. Proteomic analysis of pathogenic and attenuated alcelaphine herpesvirus 1. J Virol. 2008;82(11):5390–5397. doi: 10.1128/JVI.00094-08. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Engels M., Giuliani C., Wild P., et al. The genome of bovine herpesvirus 1 (BHV-1) strains exhibiting a neuropathogenic potential compared to known BHV-1 strains by restriction site mapping and cross-hybridization. Virus Res. 1986;6(1):57–73. doi: 10.1016/0168-1702(86)90057-2. [DOI] [PubMed] [Google Scholar]
  • 8.Galosi C. M., Barbeito C. G., Vila Roza M. V., et al. Argentine strain of equine herpesvirus 1 isolated from an aborted foetus shows low virulence in mouse respiratory and abortion models. Vet Microbiol. 2004;103:1–12. doi: 10.1016/j.vetmic.2004.07.015. [DOI] [PubMed] [Google Scholar]
  • 9.Hierholzer J. C., Killington R. A. Virus isolation and quantitation. In: Mahy B. W. J., Kangro H. O., editors. Virology methods manual. London: Academic Press; 1996. pp. 25–46. [Google Scholar]
  • 10.Jacob R. J., Price R., Bouchey D., et al. Temperature sensitivity of equine herpesvirus isolates: a brief review. SAAS Bull Biochem Biotechnol. 1990;3:124–128. [PubMed] [Google Scholar]
  • 11.Kaashoek M. J., Straver P. H., Van Rooij E. M., et al. Virulence, immunogenicity and reactivation of seven bovine herpesvirus 1.1 strains: clinical and virological aspects. Vet Rec. 1996;139:416–421. doi: 10.1136/vr.139.17.416. [DOI] [PubMed] [Google Scholar]
  • 12.Kaashoek M. J., van Engelenburg F. A., Moerman A., et al. Virulence and immunogenicity in calves of thymidine kinase- and glycoprotein E-negative bovine herpesvirus 1 mutants. Vet Microbiol. 1996;48(1–2):143–153. doi: 10.1016/0378-1135(95)00137-9. [DOI] [PubMed] [Google Scholar]
  • 13.Kaashoek M. J., Rijsewijk F. A., Ruuls R. C., et al. Virulence, immunogenicity and reactivation of bovine herpesvirus 1 mutants with a deletion in the gC, gG, gI, gE, or in both the gI and gE gene. Vaccine. 1998;16(8):802–809. doi: 10.1016/S0264-410X(97)00269-7. [DOI] [PubMed] [Google Scholar]
  • 14.Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970;227:680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  • 15.Marshall R. L., Israel B. A., Letchworth G. J., 3rd Monoclonal antibody analysis of bovine herpesvirus-1 glycoprotein antigenic areas relevant to natural infection. Virology. 1988;165:338–347. doi: 10.1016/0042-6822(88)90578-8. [DOI] [PubMed] [Google Scholar]
  • 16.Miller J. M., Whetstone C. A., Van der Maaten M. M. Abortifacient property of bovine herpesvirus type 1 isolates that represent three subtypes determined by restriction endonuclease analysis of viral DNA. Am J Vet Res. 1991;52:458–461. [PubMed] [Google Scholar]
  • 17.Muylkens B., Meurens F., Schynts F., et al. Intraspecific bovine herpesvirus 1 recombinants carrying glycoprotein E deletion as a vaccine marker are virulent in cattle. J Gen Virol. 2006;87:2149–2154. doi: 10.1099/vir.0.81969-0. [DOI] [PubMed] [Google Scholar]
  • 18.OIE. Manual of diagnostic tests and vaccines for terrestrial animals. Paris, France: OIE; 2008. Infectious Bovine Rhinotracheitis/Infectious Pustular Vulvovaginitis; pp. 752–767. [Google Scholar]
  • 19.Pastoret P. P., Burtonboy G., Aguilar-Setiena A., et al. Comparison between strains of infectious bovine rhinotracheitis virus (Bovid herpesvirus-1), from respiratory and genital origins, using polyacrylamide gel electrophoresis of structural proteins. Vet Microbiol. 1980;5:187–194. doi: 10.1016/0378-1135(80)90004-8. [DOI] [Google Scholar]
  • 20.Peterson R. B., Goyal S. M. Propagation and quantitation of animal herpesviruses in eight cell culture systems. Comp Immunol Microbiol Infect Dis. 1988;11(2):93–98. doi: 10.1016/0147-9571(88)90023-9. [DOI] [PubMed] [Google Scholar]
  • 21.Pidone C. L., Galosi C. M., Echeverria M. G., et al. Restriction endonuclease analysis of BHV-1 and -5 strains isolated in Argentina. J Vet Med B. 1999;46(7):453–456. doi: 10.1046/j.1439-0450.1999.00257.x. [DOI] [PubMed] [Google Scholar]
  • 22.Roehe P. M., Silva T. C., Nardi N. B., et al. Diferenciacaõ entre os vırus da rinotraqueıte infecciosa bovina (BHV-1) e herpesvırus da encefalite bovina (BHV-5) com anticorpos monoclonais. Pesq Vet Bras. 1997;17:41–44. doi: 10.1590/S0100-736X1997000100007. [DOI] [Google Scholar]
  • 23.Roels S., Charlier G., Lettelier C., et al. Natural case of bovine herpesvirus 1 meningoencephalitis in an adult cow. Vet Rec. 2000;146:586–588. doi: 10.1136/vr.146.20.586. [DOI] [PubMed] [Google Scholar]
  • 24.Ros C., Belak S. Studies of genetic relationships between bovine, caprine, cervine and rangiferine alphaherpes viruses and improved molecular methods for virus detection and identification. J Clin Microbiol. 1999;37:1247–1253. doi: 10.1128/jcm.37.5.1247-1253.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Ruiz-Saenz J., Jaime J., Vera V. Serological prevalence and isolation of Bovine herpesvirus-1 (BHV-1) in cattle herds from Antioquia and Valle del Cauca provinces. Rev Colomb Cienc Pecu. 2010;23:299–307. [Google Scholar]
  • 26.Smith K. C., Whitwell K. E., Mumford J. A., et al. Virulence of the V592 isolate of equid herpesvirus-1 in ponies. J Comp Pathol. 2000;122(4):288–297. doi: 10.1053/jcpa.1999.0373. [DOI] [PubMed] [Google Scholar]
  • 27.Sreenivasa B. P., Natarjan C., Rasool T. J. Restriction endonuclease analysis of DNA from Indian isolates of bovine herpesvirus 1. Acta Virol. 1996;40:315–318. [PubMed] [Google Scholar]
  • 28.van Drunen L., van den Hurk S., Myers D., Doig P. A., et al. Identification of a mutant bovine herpesvirus-1 (BHV-1) in post-arrival outbreaks of IBR in feedlot calves and protection with conventional vaccination. Can J Vet Res. 2001;65(2):81–88. [PMC free article] [PubMed] [Google Scholar]
  • 29.Weiblen R., Moraes M. P., Rebelatto M. C., et al. Bovine herpesvirus isolates. Rev Microbiol. 1996;27:208–211. [Google Scholar]
  • 30.Whestone C. A., Miller J. M., Bortner D. M., et al. Changes in the bovine herpesvirus 1 genome during acute infection, after reactivation from latency and after superinfection in the host animal. Arch Virol. 1989;106:261–279. doi: 10.1007/BF01313957. [DOI] [PubMed] [Google Scholar]

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