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Pigs in the United States were exposed to African swine fever (ASF) virus isolated from pigs in Brazil and the Dominican Republic. The former were examined for clinical response, lesions, viremia, and antibody response. Sequential blood samples were tested for the presence of ASF virus by the hemadsorption test (in swine buffy coat cell culture) and for antibody to ASF virus by the enzyme-linked immunosorbent assay. The incubation period was 3 to 5 days; inoculated pigs had fever for 8 to 16 days (mean 12.5 days) and viremia at 3 to 35 days after inoculation and few died. Inoculated pigs developed antibodies at 7 days after inoculation which were detectable until the termination of the experiment (10th month). Reinoculation of some of the surviving pigs with the homologous isolate at approximately 6 months after exposure did not induce clinical response, viremia, nor anamnestic antibody response. In contrast, challenge exposures of convalescent pigs with the Lisbon-60 viral strain approximately 5 weeks after exposure to the Brazilian strain produced death, in spite of an anamnestic antibody response.

White-tailed deer (Odocoileus virginianus) succumbed to experimental infection with virulent rinderpest (RP) virus that was also lethal to cattle and goats. The deer developed clinical signs typical of RP and died 5 and 6 days post-inoculation. Infection was confirmed by recovery of virus from blood before death, from lymph node tissue after necropsy, and demonstration of specific complement fixing antigen in those tissues. Electron micrographs of infected Vero cell cultures revealed extracellular virions and intracytoplasmic and intranuclear inclusions made of randomly distributed fibrillar strands.

White-tailed deer (Odocoileus virginianus) were infected experimentally with two strains of peste des petits ruminants virus. The response varied from fatal consequence to subclinical infection. The clinical signs and gross lesions were similar to those in goats. Virus was recovered from all the infected deer, and survivors developed specific antibodies demonstrated by complement fixation and virus neutralization tests. Survivors also resisted challenge with virulent rinderpest virus that was lethal to a control deer.

African and American forms of malignant catarrhal fever (MCF) infections were produced by inoculating blood from affected cattle into susceptible cattle. Ease of disease transmission, incubation period, volume of blood required for infection, and clinical signs were compared in 30 cattle with African MCF and in 19 with American MCF. American MCF was more difficult to transmit than was African MCF and required eight to ten times more blood as inoculum. American MCF incubation period was more than twice as long as that of the African MCF, but the disease course was three times shorter. Clinical signs were similar for the two forms; however, in the American form, the disease was more acute and a larger percentage of animals had severe diarrhea.

The enzyme-linked immunosorbent assay (ELISA) for detection of antibodies to African swine fever virus was evaluated under field conditions in the Dominican Republic. A total of 3,402 swine serums were tested by ELISA. All ELISA-positive serums (n = 224) and 426 of 2,760 ELISA-negative serums were retested by indirect immunofluorescence (IIF). There were no antibodies to ASF virus detected by IIF in ELISA-negative serums. By IIF, antibodies were detected in only a small portion of the ELISA-positive serums. The specificity and sensitivity of ELISA and IIF were investigated and discussed. It appears that poor quality serums had an effect in ELISA results. Detection of immunoglobulin (Ig) G and IgM classes of antibodies in the ELISA and IIF-positive serums were also performed and related to longevity of African swine fever virus infection. The ELISA is recommended as an efficient method in testing large number of serums; positive results are to be retested by IIF.

The causative agent of stomatitis pneumoenteritis complex was isolated in domesticated goats and Vero cell culture. It was identified immunologically and morphologically as identical with the "Peste des Petits Ruminants" virus. There were cross reactions between stomatitis pneumoenteritis complex virus isolate and rinderpest virus by immunodiffusion and complement fixation tests but no cross neutralization. Goats recovered from stomatitis pneumoenteritis complex were protected against a challenge with rinderpest virus that was lethal to control goats. Ultrastructural morphology revealed intracytoplasmic and intranuclear inclusions made up of random arrays of fibrillar strands. Pleomorphic particles budded from the plasma membrane of infected cells and enveloped virions were seen extracellularly. Specific ferritin tagging was demonstrated in the stomatitis pneumoenteritis complex virus infected cells treated with homologous and peste des petits ruminants viral antibody systems but little, if any, tagging in the heterologous rinderpest system.