Abstract
Thermal inactivation of rabies and several other rhabdoviruses was studied using virus suspended in several different diluents. Rabies serogroup viruses were more stable than Kern Canyon or vesicular stomatitis viruses. Limited studies of two fish rhabdoviruses requiring low temperatures (less than 33 C) for replication indicated that they were not markedly more thermolabile than rabies virus. Bovine serum protein components in complex cell culture media stabilized virus at 56 C, but at temperatures of less than or equal to 37 C, sodium tris (hydroxymethyl)-aminomethane (NT) buffer containing ethylenediaminetetraacetic acid (EDTA) (NTE) was a much more efficient stabilizer of virus infectivity. Chelating agents EDTA and ethyleneglycol-bis-(beta-aminoethyl ether)tetraacetic acid were equally efficient in protection of rabies virus infectivity; the effect of each was lost when excess Ca2+ was added. Bovine serum in NT or NTE buffers produced a thermostabilizing effect at 37 C not provided by the same serum concentration in complex cell culture media. Bovine serum was more efficient than EDTA in stabilizing virus infectivity during repeated cycles of freezing and thawing.
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Selected References
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- BOULGER L. R., PORTERFIELD J. S. Isolation of a virus from Nigerian fruit bats. Trans R Soc Trop Med Hyg. 1958 Sep;52(5):421–424. doi: 10.1016/0035-9203(58)90127-5. [DOI] [PubMed] [Google Scholar]
- Bishai F. R., Labzoffsky N. A. Stability of different viruses in a newly developed transport medium. Can J Microbiol. 1974 Jan;20(1):75–80. doi: 10.1139/m74-012. [DOI] [PubMed] [Google Scholar]
- Clark H. F., Koprowski H. Isolation of temperature-sensitive conditional lethal mutants of "fixed" rabies virus. J Virol. 1971 Mar;7(3):295–300. doi: 10.1128/jvi.7.3.295-300.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Clark H. F., Soriano E. Z. Fish rhabdovirus replication in non-piscine cell culture: new system for the study of rhabdovirus-cell interaction in which the virus and cell have different temperature optima. Infect Immun. 1974 Jul;10(1):180–188. doi: 10.1128/iai.10.1.180-188.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Clark H. F., Wiktor T. J. Plasticity of phenotypic characters of rabies-related viruses: spontaneous variation in the plaque morphology, virulence, and temperature-sensitivity characters of serially propagated Lagos bat and Mokola viruses. J Infect Dis. 1974 Dec;130(6):608–618. doi: 10.1093/infdis/130.6.608. [DOI] [PubMed] [Google Scholar]
- Clark H. F., Wiktor T. J. Temperature-sensitivity characteristics distinguishing substrains of fixed rabies virus: lack of correlation with plague-size markers or virulence for mice. J Infect Dis. 1972 Jun;125(6):637–646. doi: 10.1093/infdis/125.6.637. [DOI] [PubMed] [Google Scholar]
- DULBECCO R., VOGT M. Plaque formation and isolation of pure lines with poliomyelitis viruses. J Exp Med. 1954 Feb;99(2):167–182. doi: 10.1084/jem.99.2.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Deutsch V., Berkaloff A. Analyse d'un mutant thermolabile du virus de la stomatite vésiculaire (VSV. Ann Inst Pasteur (Paris) 1971 Jul;121(1):101–106. [PubMed] [Google Scholar]
- Dimmock N. J. Differences between the thermal inactivation of picornaviruses at "high" and "low" temperatures. Virology. 1967 Feb;31(2):338–353. doi: 10.1016/0042-6822(67)90179-1. [DOI] [PubMed] [Google Scholar]
- FINNEY D. J., HAZLEWOOD T., SMITH M. J. Logarithms to base 2. J Gen Microbiol. 1955 Apr;12(2):222–225. doi: 10.1099/00221287-12-2-222. [DOI] [PubMed] [Google Scholar]
- Gauntt C. J. Fragmentation of RNA in virus particles of rhinovirus type 14. J Virol. 1974 Mar;13(3):762–764. doi: 10.1128/jvi.13.3.762-764.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holland J. J., Kohne D., Doyle M. V. Analysis of virus replication in ageing human fibroblast cultures. Nature. 1973 Oct 12;245(5424):316–319. doi: 10.1038/245316a0. [DOI] [PubMed] [Google Scholar]
- Holloway A. F., Wong P. K., Cormack D. V. Isolation and characterization of temperature-sensitive mutants of vesicular stomatitis virus. Virology. 1970 Dec;42(4):917–926. doi: 10.1016/0042-6822(70)90340-5. [DOI] [PubMed] [Google Scholar]
- Kemp G. E., Causey O. R., Moore D. L., Odelola A., Fabiyi A. Mokola virus. Further studies on IbAn 27377, a new rabies-related etiologic agent of zoonosis in nigeria. Am J Trop Med Hyg. 1972 May;21(3):356–359. [PubMed] [Google Scholar]
- MACPHERSON I., STOKER M. Polyoma transformation of hamster cell clones--an investigation of genetic factors affecting cell competence. Virology. 1962 Feb;16:147–151. doi: 10.1016/0042-6822(62)90290-8. [DOI] [PubMed] [Google Scholar]
- Repik P., Flamand A., Clark H. F., Obijeski J. F., Roy P., Bishop D. H. Detection of homologous RNA sequences among six rhabdovirus genomes. J Virol. 1974 Jan;13(1):250–252. doi: 10.1128/jvi.13.1.250-252.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sedwick W. D., Wiktor T. J. Reproducible plaquing system for rabies, lymphocytic choriomeningitis,k and other ribonucleic acid viruses in BHK-21-13S agarose suspensions. J Virol. 1967 Dec;1(6):1224–1226. doi: 10.1128/jvi.1.6.1224-1226.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shope R. E., Murphy F. A., Harrison A. K., Causey O. R., Kemp G. E., Simpson D. I., Moore D. L. Two African viruses serologically and morphologically related to rabies virus. J Virol. 1970 Nov;6(5):690–692. doi: 10.1128/jvi.6.5.690-692.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sokol F., Clark H. F., Wiktor T. J., McFalls M. L., Bishop D. H., Obijeski J. F. Structural phosphoproteins associated with ten rhabdoviruses. J Gen Virol. 1974 Sep;24(3):433–445. doi: 10.1099/0022-1317-24-3-433. [DOI] [PubMed] [Google Scholar]
- Thormar H. A comparison of cocal and vesicular stomatitis virus, serotypes New Jersey and Indiana. Virology. 1967 Feb;31(2):323–328. doi: 10.1016/0042-6822(67)90177-8. [DOI] [PubMed] [Google Scholar]
- Turner G. S., Kaplan C. Some properties of fixed rabies virus. J Gen Virol. 1967 Oct;1(4):537–551. doi: 10.1099/0022-1317-1-4-537. [DOI] [PubMed] [Google Scholar]
- WALLIS C., MENICK J. L. Cationic stabilization--a new property of enteroviruses. Virology. 1962 Apr;16:504–506. doi: 10.1016/0042-6822(62)90234-9. [DOI] [PubMed] [Google Scholar]
- WALLIS C., YANG C. S., MELNICK J. L. Effect of cations on thermal inactivation of vaccinia, herpes simplex, and adenoviruses. J Immunol. 1962 Jul;89:41–46. [PubMed] [Google Scholar]
- WOESE C. Thermal inactivation of animal viruses. Ann N Y Acad Sci. 1960 Jan 13;83:741–751. doi: 10.1111/j.1749-6632.1960.tb40943.x. [DOI] [PubMed] [Google Scholar]
- YOUNGNER J. S. Thermal inactivation studies with different strains of poliovirus. J Immunol. 1957 Apr;78(4):282–290. [PubMed] [Google Scholar]
