Studies on swinepox virus: fluorescence and light microscopy of infected cell cultures.
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Biomedical subjects
Publications and source records attributed to R C Meyer.
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Swinepox virus was successfully adapted to the PK-15 cell line, but not the MDBK cell line. Virus titers obtained in the PK-15 host cell system were comparable to diploid swine kidney cell cultures.
Newborn, germfree piglets were susceptible to Escherichia coli associated with human, nonenteric infections and should provide a useful model in the study of generalized E. coli infections.
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The oral administration of an 18-hr broth culture of Escherichia coli 06: isolated from a cat to 3-day-old gnotobiotic (germ-free) piglets resulted in bacteremia and polyserositis. Sixteen pigs, selected from four litters, were used in the study. E. coli of the same serotype employed was the only bacterial agent demonstrable and recovered from moribund and dead piglets. Attempts to recover virus or PPLO (mycoplasma) from these animals were unsuccessful. A polyserositis syndrome was not encountered among neonatal pigs in experiments with 14 other serotypes of E. coli; hence it was considered to be a syndrome closely associated with the infection caused by this particular strain of E. coli.
Three strains of Escherichia coli isolated from infectious processes in a calf, a dog, and a cat were examined for their capacity to produce disease or death, or both, in newborn gnotobiotic piglets. The O groups represented by these particular strains of E. coli were O4: (canine origin), O6: (feline origin), and O39: (bovine origin). All three isolates upon oral administration proved to be pathogenic. Infection with the E. coli O4: (canine) or O39: (bovine) consistently produced signs of enteric coli-bacillosis and death in all 1- and 3-day-old piglets within 24 to 48 hr. The O6: (feline) isolate, on the other hand, produced a marked polyserositis and generally required 6 to 7 days to kill a piglet. Only the respective type of E. coli used in the particular trial was recovered from the diseased piglets. These findings suggest the possible role of domestic animals and household pets in the spread of potentially pathogenic E. coli to other species.
In a group of 112 cats, examined during an outbreak of diarrhea, 104 (92.8%) yielded Escherichia coli with identifiable O groups as compared to 12 (21.8%) of 55 control cats apparently free of intestinal ailments. E. coli group O6 occurred in 49.1% of the cats with diarrhea, and persisted in this group of cats at about the same rate when examined for a period of ten months. E. coli group O6 was not isolated from the control group. Specimens were also collected from dogs with various clinical signs. E. coli O4 and O6 strains appear to be important potential pathogens for canine species and were found to spread from one dog to another when in close contact. E. coli group O4 was identified in ten and O6 in three of 14 dogs examined. All isolates in which the O group could be identified were hemolytic.
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Thirteen specific-pathogen-free pigs were used in an experiment to determine the pathogenicity of IBR virus for pigs. Three pigs were used as controls, eight were exposed to IBR virus by either the intravenous, subcutaneous, intratracheal, or intranasal route, and two pigs served as contact controls. The clinical response consisted of a temperature rise, depression and variable lymphocytosis. The major tissue alterations were interstitial pneumonitis, and peribronchiolitis with round cell aggregates and giant cell formation. IBR virus was not recovered from any of the pigs. A serologic response was detected in only the pig injected intravenously.
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Pneumonia resulted when a porcine entero-virus, ECPO-6, was inoculated intranasally into four and six week old, colostrum deprived, specific pathogen free piglets. Clinical signs consisted of mild depression, rapid breathing with rectal temperatures reaching 104-105 F five to six days after infection. Pneumonic lesions, both gross and microscopic were present 21 days post infection. Although the virus was readily isolated from the cecal contents of infected pigs three weeks after infection the virus was not recovered from infected lungs after the first 7-10 days.
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