Because Cryptosporidium parvum oocysts are very resistant to conventional water treatment processes, including chemical disinfection, we determined the kinetics and extent of their inactivation by monochromatic, low-pressure (LP), mercury vapor lamp UV radiation and their subsequent potential for DNA repair of UV damage. A UV collimated-beam apparatus was used to expose suspensions of purified C. parvum oocysts in phosphate-buffered saline, pH 7.3, at 25°C to various doses of monochromatic LP UV. C. parvum infectivity reductions were rapid, approximately first order, and at a dose of 3 mJ/cm 2 03؍( J/m 2 ), the reduction reached the cell culture assay detection limit of ϳ3 log 10 . At UV doses of 1.2 and 3 mJ/cm 2 , the log 10 reductions of C. parvum oocyst infectivity were not significantly different for control oocysts and those exposed to dark or light repair conditions for UV-induced DNA damage. These results indicate that C. parvum oocysts are very sensitive to inactivation by low doses of monochromatic LP UV radiation and that there is no phenotypic evidence of either light or dark repair of UV-induced DNA damage.Cryptosporidium parvum is an important health-related waterborne pathogen that is ubiquitous in surface and source waters (16) and very resistant to conventional water treatment processes (9). Although conventional water filtration systems achieve some removal (9), chemical disinfection by chlorination is incapable of achieving appreciable inactivation of C. parvum oocysts at practical disinfectant doses and contact times (7,23). Previous studies using the in vitro viability assays of excystation and vital dye staining suggested that C. parvum oocysts are also very resistant to monochromatic low-pressure (LP) UV radiation (5, 21) and much more resistant than the enteric viruses that have been proposed as the basis for determining UV dosimetry in water and wastewater treatment (11,12,19). However, recent studies using in vivo animal bioassays indicate that polychromatic medium-pressure mercury lamp UV as well as LP UV extensively reduce C. parvum oocyst infectivity at relatively low doses (4, 6).Animal bioassays are considered the "gold standard" for assessing Cryptosporidium oocyst infectivity (14). However, they are costly, require tedious and lengthy procedures for handling animals and scoring for infection, give variable and imprecise estimates of infectious dose and infectivity concentrations, and raise ethical concerns about the use of experimental animals when alternative infectivity assays are available (24). In vitro cell culture infectivity assays using fluorescent antibodies against living stages of C. parvum (27, 32) are reliable and convenient alternatives to animal infectivity assays, but comparisons of cell culture and animal infectivity assays for assessing UV inactivation of Cryptosporidium oocysts have not yet been reported in the literature. In this study, we compared mouse and cell culture infectivity assays in LP UV disinfection experiments on C. parvum oocysts. The kinetics ...