IFN-gamma gene was disrupted by homologous recombination in A3-1 embryonic stem cells. Germinally transmitted chimeric mice were successfully obtained and backcrossed with C57BL/6 (B6) mice 5 or 6 times. Deficiency of IFN-gamma in homozygous mice was confirmed by northern blot analysis of spleen cells stimulated with phorbor esther and calcium ionophore and also by IFN-gamma production in the culture supernatant of spleen cells stimulated with the same reagents. B6 mice lacking IFN-gamma were infected intraperitoneally (ip) with 10(6) PFU of JHMV and monitored for their survival. Approximately 90% of the mice died at 50 days post-infection (pi) and the mean survival time was 28 days. Mice sacrificed at 3 weeks pi showed severe peritonitis accompanying the accumulation of a viscous fluid in the abdominal and thoracic cavities. Microscopically, the disease was characterized by disseminated granulomatous inflammation and exudative fibrinous serositis in the abdominal cavity. Infectious virus was isolated in most tissues including the liver, spleen, kidney, pancreas and lung during the experimental periods. The disease was not observed in wild-type or heterozygous littermates infected i.p. with JHMV. These results suggest that IFN-gamma plays a critical role in MHV infection in mice. This experimental model may provide a unique opportunity to address the pathogenesis of virus-induced peritonitis such as feline infectious peritonitis in cats.