Biopolym. Cell. 2011; 27(2):162-164.
Short Communications
Persistence of viral RNA in the brain of experimentally infected mice with coxsackievirus B5
1Stipalova D., 1Sojka M., 1Borsanyiova M., 1Badurova M., 1Marosova L., 2Sobotova Z., 1Bopegamage S.
  1. Department of Virology, Slovak Medical University
    12, Limbova St., Bratislava, Slovak Republic, 83303
  2. National Reference Centres, Public Health Office of the Slovak Republic
    52, Trnavska St., Bratislava, Slovak Republic, 82645

Abstract

The aim of our study was to follow the persistence of viral RNA in selected organs of experimentally infected with coxsackievirus (CV) B5 strains from different sources such as a patient’s sample, an environmental sample and a prototype virus strain. Methods. CD-1 mice were infected with CVB5 strain Faulkner the prototype, CVB5 – isolate from treated sewage waste and isolate from patient’s stool sample both identified as CVB5. The viral RNA was detected by RT-PCR using enterovirus primers specific for the non-coding 5' region. Results. We observed presence of RNA in the brain and heart of mice infected with isolate from patient’s stool at day 45 post infection (p. i.). Conclusion. We conclude that CVB5 persists in the brain and heart after oral infection of CD1 mice. The relevance of viral persistence maybe related viral origin and the genetics.
Keywords: coxsackievirus B5, mouse, brain, persistence

References

[1] Lindberg A. M., Polacek C. Molecular analysis of the prototype coxsackievirus B5 genome Arch. Virol 2000 145, N 2 P. 205–221.
[2] Cree B. C., Bernardini G. L., Hays A. P., Lowe G. A fatal case of coxsackievirus B4 meningoencephalitis Arch Neurol 2003 60, N 1 P.107–112.
[3] Motusova J., Sojka M., Stipalova D. Standardization of plaque purification for coxsackieviruses Coxsackieviruses and animal models: Basics and experiences of our laboratory / Ed. S. Bopegamage Bratislava: Asklepios, 2008 P. 91–95.
[4] Bopegamage S., Kovacova J., Vargova A., Motusova J., Petrovicova A., Benkovicova M., Gomolcak P., Bakkers J., van Kuppeveld F., Melchers W. J., Galama J. M. Coxsackie B virus infection of mice: inoculation by the oral route protects the pancreas from damage, but not from infection J. Gen. Virol 2005 86, pt 12 P. 3271–3280.
[5] Bopegamage S., Borsanyiova M., Vargova A., Petrovicova A., Benkovicova M., Gomolcak P. Coxsackievirus infection of mice I. Viral kinetics and histopathological changes in mice experimentally infected with coxsackieviruses B3 and B4 by the oral route Acta Virol 2003 47, N 4 P. 245–251.
[6] De Leeuw N., Melchers W. J. G., Willemse D. F. M., Balk A. H. M. M., de Jonge N., Galama J. M. D. The diagnostic value of PCR for diagnosis of enteroviral infections Serodiag. Immunother. Infect. Dis. J 1994 6, N 4 P. 189–195.
[7] Andreoletti L., Hober D., Becquart P., Belaich S., Copin M. C., Lambert V., Wattre P. Experimental CVB3-induced chronic myocarditis in two murine strains: evidence of interrelationships between virus replication and myocardial damage in persistent cardiac infection J. Med. Virol 1997 52, N 2 P. 206–214.
[8] Kandolf R., Klingel K., Zell R., Selinka H. C., Raab U., Schneider-Brachert W., Bultmann B. Molecular pathogenesis of enterovirus-induced myocarditis: virus persistence and chronic inflammation Intervirology 1993 35, N 1–4 P. 140–151.
[9] Klingel K., Hohenadi C., Canu A., Albrecht M., Seemann M., Mall G., Kandolf R. Ongoing enterovirus-induced myocarditis is associated with persistent heart muscle infection: quantitative analysis of virus replication, tissue damage, and inflammation Proc. Natl Acad. Sci. USA 1992 89, N 1 P. 314–318.
[10] Chapman N. M., Kim K.-S. Persistent coxsackievirus infection: Enterovirus persistence in chronic myocarditis and dilated cardiomyopathy Curr. Top. Microbiol. Immunol 2008 323 P. 275–292.
[11] Klingel K. Molecular biologic detection of virus infection myocarditic and dilated cardiomyopathy Myocarditis from bench and bedside / Ed. L. T. Coopers, Jr New Jersey: Humana press, 2003 P. 295–324.
[12] Gow J. W., Behan W. M. H., Cash P., Simpson K., Behan P. O. Genomic and template RNA transcription in a model of persistent enteroviral infection J. NeuroVirol 1997 3, N 1 P. 76–82.
[13] Pelletier I., Couderc T., Borzakian S., Wyckoff E., Crainic R., Ehrenfeld E., Colbere-Garapin F. Characterization of persistent poliovirus mutants selected in human neuroblastoma cells Virology–1991 180, N 2 P. 729–737.
[14] Tracy S. The genome of the Group B coxsackieviruses Coxsackieviruses – a general update / Eds M. Bendinelli, H. Friedman New York: Plenum Publ., 1988 P. 19–33.
[15] Dunn J. J., Bradrick S. S., Chapman N. M., Tracy S. M., Romero J. R. The stem loop II within the 5' nontranslated region of clinical coxsackievirus B3 genomes determines cardiovirulence phenotype in a murine model J. Infect. Dis 2003 187, N 10 P. 1552–1561.