TY - JOUR T1 - Ozone inactivation of cell-associated viruses. A1 - Emerson, M A LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English LA - English YR - 1982 UL - http://buscaintegrada.pucsp.br/vufind/Record/pubmed-241881 AB - The inactivation of HEp-2 cell-associated poliovirus (Sabin 1) and coxsackievirus A9 was investigated in three experimental systems, using ozone as a disinfectant. The cell-associated viral samples were adjusted to a turbidity of 5 nephelometric turbidity units. The cell-associated poliovirus and coxsackievirus samples demonstrated survival in a continuous-flow ozonation system at applied ozone dosages of 4.06 and 4.68 mg/liter, respectively, for 30 s. Unassociated viral controls were inactivated by the application of 0.081 mg of ozone per liter for 10 s. Ultrasonic treatment of cell-associated enteric viruses did not increase inactivation of the cell-associated viruses. The batch reactor with a declining ozone residual did not effect total inactivation of either cell-associated enteric virus. These cell-associated viruses were completely inactivated after exposure to ozone in a batch reactor using continuous ozonation. Inactivation of cell-associated poliovirus required a 2-min contact period with an applied ozone dosage of 6.82 mg/liter and a residual ozone concentration of 4.70 mg/liter, whereas the coxsackievirus was completely inactivated after a 5-min exposure to an applied ozone dosage of 4.81 mg/liter with an ozone residual of 2.18 mg/liter. These data indicate that viruses associated with cells or cell fragments are protected from inactivation by ozone concentrations that readily inactivate purified virus. The cell-associated viral samples used in this research contained particles that were 10 to 15 microns in size. Use of a filtration system before ozonation would remove these particles, thereby facilitating inactivation of any remaining viruses associated with cellular fragments. KW - Research Article KW - General Microbial Ecology KW - Metabolism, Growth, and Industrial Microbiology KW - Methods KW - Food Microbiology and Toxicology KW - Errata ER -