The nucleotide sequences have been determined and compared from cloned cDNA genes coding for the foot-and-mouth disease virus (FMDV) The cause of the antigenic variation in FMDV has received some study. In vitro, spontaneous conditional-lethal mutants have been isolated at a rate as high as 10-3o0 per plaque-forming unit (pfu) for temperature-sensitive mutants (7). Although this rate is high when compared to DNA viruses [presumably due to lack of proofreading activity in the RNA replicase (8-10)], it is no higher than mutation rates in other RNA viruses (9). Several research groups have suggested that under the pressure of field outbreaks mutants are selected that are not effectively neutralized in the immunized or convalescent animal populations (9-13). This "immune selection" may be accelerated by the existence of unvaccinated or only partially protected livestock or unprotected wild animal hosts situated near livestock production regions (3,12). Obviously, the multiplicity of animal hosts (1) also contributes to the persistence and variability of FMDV. The number of subtypes is higher in areas where the virus is indigenous in wild animal populations, for example, in Africa (14), and in areas where the virus is endemic in animals transported for breeding, trade, or slaughter, as in South America (4