Live attenuated vaccine strains, such as type I nonreplicating uracil auxotroph mutants, are highly effective in eliciting lifelong immunity to virulent acute infection by Toxoplasma gondii. However, it is currently unknown whether vaccine-elicited immunity can provide protection against acute infection and also prevent chronic infection. To address this problem, we developed nonreverting, nonreplicating, live attenuated uracil auxotroph vaccine strains in the type II ⌬ku80 genetic background by targeting the deletion of the orotidine 5=-monophosphate decarboxylase (OMPDC) and uridine phosphorylase (UP) genes. Deletion of OMPDC induced a severe uracil auxotrophy with loss of replication, loss of virulence in mice, and loss of the ability to develop cysts and chronic infection. Vaccination of mice using type II ⌬ku80 ⌬ompdc mutants stimulated a fully protective CD8؉ T celldependent immunity that prevented acute infection by type I and type II strains of T. gondii, and this vaccination also severely reduced or prevented cyst formation after type II challenge infection. Nonreverting, nonreplicating, and non-cyst-forming ⌬ompdc mutants provide new tools to examine protective immune responses elicited by vaccination with a live attenuated type II vaccine.T oxoplasma gondii is an obligate intracellular parasite with an extremely broad host range inclusive of most birds and virtually all mammals (1). T. gondii chronically infects approximately one-third of the human population (2). Three major strain types are found in North America and Europe, and these type I, II, or III strains differ with respect to their virulence traits in mice (3). Type I strains are considered to be highly virulent, type II strains have low virulence, and type III strains are considered to be avirulent. Following acute infection by type II strains of T. gondii, a chronic infection is established. Chronic infection is characterized by slow-growing bradyzoite forms within tissue cysts in brain, muscle, and eye (4), and infection is considered to be lifelong (5, 6). Reactivated infection during AIDS or immune suppression may cause a severe and difficult to treat toxoplasmic encephalitis (7) or recurrent ocular toxoplasmosis (8). Vaccination against Toxoplasma is difficult due to the existence of multiple antigenically distinct strain types and multiple antigenically distinct developmental stages. Toxoplasma also can effectively escape immunity by the development of a chronic encysted stage that is not easily cleared by immune responses.Antigen-based vaccine formulations provide only a partially protective immunity and do not prevent the establishment of tissue cysts and chronic infection following exposure to T. gondii (9). Immunization with T. gondii extracts or killed noninvasive parasites also fails to elicit significant immunity to reinfection with T. gondii (10, 11). Suboptimal vaccine priming using antigen-based vaccine formulations is not surprising in view of the requirement for populations of CD8 ϩ and CD4 ϩ T cells that produce the inter...