Evaluation of the effectiveness of the SurePure Turbulator ultraviolet-C irradiation equipment on inactivation of different enveloped and non-enveloped viruses inoculated in commercially collected liquid animal plasma.

The objective of this study was to evaluate the effectiveness of the SurePure Turbulator ultraviolet-C (UV-C, 254 nm wavelength) irradiation equipment on inactivation of different enveloped and non-enveloped viruses in commercially collected liquid animal plasma. Specifically, Pseudorabies virus (PRV), Porcine reproductive and respiratory syndrome virus (PRRSV), Porcine epidemic diarrhea virus (PEDV), Bovine viral diarrhea virus (BVDV), Classical swine fever virus (CSFV), Swine influenza virus (SIV) as enveloped viruses and Porcine parvovirus (PPV), Swine vesicular disease virus (SVDV), Porcine circovirus type 2 (PCV-2) and Senecavirus A (SVA) as non-enveloped viruses, were inoculated in bovine or porcine plasma and subjected to different UV-C irradiation doses (0, 750, 1500, 3000, 6000 and 9000 J/L) using an UV-C device developed for opaque liquid working under turbulent flow. The enveloped viruses tested were inactivated at < 3000 J/L of UV-C, being the dose needed to inactivate 4 log TCID50 (4D) of 1612 J/L for PRV,1004 J/L for PRRSV, 1953 J/L for PEDV, 1639 J/L for SIV, 1641 J/L for CSFV and 1943 J/L for BVDV. The non-enveloped viruses tended to have higher 4D values: 2161 J/L for PPV, 3223 J/L for SVA and 3708 J/L for SVDV. Because the initial viral concentration was <4.0 Log for PCV-2, it was not possible to calculate the 4D value for this virus. In conclusion, these results demonstrated that the SurePure Turbulator UV-C treatment system is capable of inactivating significant levels of swine viruses inoculated in commercially collected porcine or bovine plasma. It was concluded that irradiation with UV-C can provide an additional redundant biosafety feature in the manufacturing process of spray-dried animal plasma.

[Photosensitizing properties of 3,3'-diethylthiacarbocyanine in biological media].

The objective of the study is elucidation of perspectives of 3,3'-diathylcarbocyaine application as a photosensitizer for curing viral infections by photodynamic therapy. Lipid-containing bacteriophage PM-2 of Pseudoalteromonas espejiana was used as a model. The testing was carried out at a special installation modeling photodynamic exposure conditions towards a non-fractionated phage lysate. 3,3'-DECC demonstrated a rapid photo-bleaching when added tothe phage lysate but not to water. The initial rate of PM-2 phage photoinactivation was proportional to the square concentration of the dye in the range of 0.5-9 µmol/L. This confirms a hypothesis that the dimer is the principal photochemically active form of the dye. An improved ability to form dimers was found in the dye in the phage lysate (10-folds better than in the water). The dye formed a stable adduct with the bacteriophage material. This adduct had an extinction maximum at λ(max) = 594 nm and demonstrated the properties of a polymer (sedimentation under a low-speed centrifugation).

Targeting host cells harbouring viruses with radiolabeled antibodies.

Existing antiviral therapies produce a therapeutic effect by suppressing viral replication and reducing viral burden and the associated inflammatory reaction. However, infection with many viruses results in chronic infections that cannot be eradicated by the immune response or available antiviral drugs. As viruses are obligate intracellular pathogens, it should be possible to eradicate chronic infections by targeting and eliminating the infected host cells. Radioisotope-conjugated antibodies that specifically bind viral antigens can deliver cytotoxic radiation to virally infected cells. This approach was recently shown to target and eliminate HIV-1-infected cells in vitro and in mouse models, and provides a new approach for eliminating virally infected cells.

The effect of ultraviolet radiation on human viral infections.

Exposure to UV radiation is recognized to suppress cell-mediated immunity and therefore could adversely affect the course of a viral infection. Rodent models of viral infection confirm this possibility but the situation in human subjects is not so clear, apart from two exceptions. These are herpes simplex, in which sunlight exposure can cause reactivation, and certain papillomavirus types in which sunlight exposure can lead to the development of nonmelanoma skin cancer. In both cases, there are UV response elements in the viral genomes that alter the normal interactions between the viruses and the host following exposure, and UV-induced effects on the immune response occur in addition. These complex mechanisms are discussed, and the situation regarding UV radiation and viral exanthems plus other viruses, including the retroviruses, summarized. Finally viral vaccination is considered in the context of UV exposure and the importance of the host's genetic background emphasized. Further research is required to evaluate whether sunlight can significantly affect the resistance to common viral infections and vaccines.

[Unexpected effects of a whole body irradiation on the mortality rate of baby mice after an experimental infection with the vesicular stomatitis virus (VSV)]. / Unerwartete Effekte einer Ganzkörperbestrahlung auf die Mortalitätsrate von Babymäusen nach einer experimentellen Infektion mit dem Virus der Stomatitis vesicularis (VSV).

The effect of total body irradiation of baby mice or their pregnant mothers with surface doses of 3.9 Gy on the mortality rate after infection of the baby mice with VSV has been studied. Irradiation of the newborns had no influence on the mortality rate of the infected animals. Irradiation of the pregnant animals--and the foetuses in utero--caused an astonishing decrease of the mortality rate of the infected baby mice for about 50% in compare to the non irradiated controls.

Quantitative studies of the inflammatory process in fatal viral meningoencephalitis.

The pathogenesis of acute meningoencephalitis induced in adult mice by intravenous inoculation with Semliki Forest virus has been assessed by counting cells in cerebrospinal fluid (CSF). Meningitis was first apparent on day 4 and, by the time that animals were moribund 2 days later, each microliter of CSF contained in excess of 10,000 mononuclear cells. The following conclusions were made concerning this very considerable inflammatory response: a) Complete suppression of cellular infiltration makes no difference to the clinical disease. b) No correlation is apparent between inflammation and levels of circulating antibody. c) Participation of thymus-derived lymphocytes (T cells) is essential for full expression, though not for initiation, of cellular invasion. d) There is evidently no requirement for lymphocytes recently derived from thymus or for any humoral factor secreted by thymus tissue. e) T cells entering the recirculating pool more than 6 weeks or less than about 1 week prior to inoculation of virus are equally effective in promoting inflammation. f) The T cells apparently act directly by enhancing infiltration of other blood-borne mononuclears into the brain and CSF.