Toxoplasmosis in Lower Mammals*

SYNOPSIS. Sera from 270 domestic and wild mammals were tested for antibodies against Toxoplasma gondii by the indirect hemagglutination method. The specificity of reactions was determined by the hemagglutination-inhibition test. Positive results at a titer of 1:64 were given by 10 of 138 cattle, 3 of 74 swine, 1 of 8 cats and none of 3 horses. Of the wild animals tested, only 1 of 9 woodchucks was positive; 17 raccoons, 14 opossums and 7 skunks were negative.     

Toxoplasmosis in Sheep

The presence of Toxoplasma gondii in the diaphragm was correlated with the dye test titres in 174 sheep. In 94 of these the presence of the parasite was also correlated with the haemoglobin (Hb) type. T. gondii was recovered from 3 % of the sheep with titres < 1/16, compared with 30 % of those with titres 1/16 and 70 % of those with titres ≥ 1/32. The results indicate that the distinction between serologically positive and negative individuals at a final serum dilution of 1/16 is justified. Some evidence was found that the parasite is easier to recover from dye test positive mature sheep than from dye test positive lambs. Of the 174 sheep, 143 were examined at random among 186 sheep culled or cast for age during a 4-year period from 1 flock in which the prevalence of Toxoplasma antibodies was representative for flocks in the southern Norway, and T. gondii was recovered from 53 (37 %) of these. It was concluded that 10—15 % of the lamb carcases and 25—37 % of the carcases from mature sheep in this country have T. gondii in their muscles detectable by the peptic digestion technique. A possible genetical influence on the infection was indicated by the higher frequency of recoveries of T. gondii from sheep with Hb type B than from sheep with the Hb types A or AB, but the number of individuals with Hb type B was too small to demonstrate statistically significant differences. The epidemiological importance of infected sheep carcases is discussed.     

Feline Toxoplasmosis from Acutely Infected Mice and the Development of Toxoplasma Cysts*

SYNOPSIS. The development of Toxoplasma cysts was studied in mice inoculated with tachyzoites by several routes. After 1–30 days of infection, murine tissues were examined microscopically, and portions or whole carcasses were fed to mice and cats. The feces of the cats were examined for oocyst shedding. Cyst-like structures containing distinct PAS-positive granules were first seen after 3 days of infection with tachyzoites, and became numerous by 6 days. Argyrophilic walls were first seen after 6 days, and became numerous by 16 days of infection with tachyzoites. Prepatent periods to oocyst shedding (PPO) were either “short” (3–10 days) or “long” (19–48 days). The “short” PPO was found only in cats that had ingested mice infected for 3 days or longer, and was related to the development of PAS-positive granules in T. gondii, and to high, 60–100%, oral infectivity rates for cats. The “long” PPO followed the ingestion of mice infected for only 1–2 days, and was related to tachyzoites without distinct PAS-positive granules and low, 32% or less, infectivity for cats. The “long” PPO followed also the ingestion of oocysts and the parenteral inoculation of tachyzoites, bradyzoites, or sporozoites. Using the “short” PPO as a criterion for detecting cysts in tissues, it was shown that (a) numerous cysts developed in mice 5 days after inoculation with tachyzoites, 7–9 days after inoculation with cysts, and 9–10 days after inoculation with oocysts, and (b) cysts developed faster and more frequently in the brain and muscle than in lungs, liver, spleen, and kidneys of mice inoculated with tachyzoites.     

Life Cycle of Isospora rivolta (Grassi, 1879) in Cats and Mice*

SYNOPSIS. The endogenous development of Isospora rivolta (Grassi) was studied in cats fed oocysts, and was compared with the endogenous cycle after feeding them mice infected with I. rivolta. For the mouse-induced cycle, 14 newborn cats were killed 12 to 240 h after having been fed mesenteric lymph nodes and spleens of mice. Asexual and sexual development occurred throughout the small intestine, in epithelial cells of the villi and glands of Lieberkuhn. The number of asexual generations was not determined with certainty, but there were at least 3 structurally different meronts. Type I meronts appeared at 12–48 h postinoculation (HPI). They were 8.5(6–13) × 5.1(3–6) μm, contained 2–8 merozoites, and divide by binary division or endodyogeny. Type II meronts were multinucleate merozoite-shaped meronts within a single parasitophorous vacuole. They were found at 48–172 HPI and measured 12.6(9–18) × 9.8(9–13) μm. Individual multinucleate merozoite-shaped meronts were 7–13 × 3–5 μm in sections and contained 2–30 slender (5.5 × 1.0 μm) merozoites. Type III meronts occurred at 72–192 HPI and gamonts at 72–96 HPI. Mature microgamonts measured 11.3(9–15) × 8.0(6–9) μm in sections and up to 21.5 × 14 μm in smears, and contained up to 70 microgametes. Macrogamonts measured 13.3(11–18) × 9.0(5–13) μm in sections and 18 × 16 μm in smears. Oocysts were 10–15 × 9–15 μm in sections and 19.8(17–24) × 18.0(17–23) μm in fixed and stained smears. Unsporulated oocysts in feces were 22.3(18–25) × 19.7(16–23) μm and spomlated oocysts 25.4(23–29) × 23.4(20–26) μm. Sporulation was completed within 24 h at 22–26 C. For the study of the oocyst-induced cycle in cats, 18 newborn cats were killed between 6 and 192 HPI. The endogenous development was essentially similar to the mouse-induced cycle, but merogony and gametogony occurred 12–48 h later than in the latter cycle. Isospora rivolta was pathogenic for newborn but not for weaned cats. Newborn cats fed 10⁵ sporocysts or infected mice usually developed diarrhea 3–4 days after inoculation. Microscopically, desquamation of the tips of the villi and cryptitis were seen in the ilium and cecum in association with meronts and gamonts. For the study of the development of I. rivolta in mice, mice were killed from day 1 to 23 months after having been fed 10⁵–10⁵ sporocysts, and their tissues were examined for the parasites microscopically, and by feeding to cats. The following conclusions were drawn. (A) Isospora rivolta most frequently invaded the mesenteric lymph nodes of mice and remained there for 23 months at least. It also invaded the spleen, liver, and skeletal muscles of mice. This species could not be passed from mouse to mouse. Sporozoites increased in size from ?6.8 × 4.9 μm on day 1 to ?13.4 × 6.9 μm on day 31 postinoculation. Division was not seen. Prepatent period was 4–7 days and patent periods ranged from 2 to several weeks.     

Ovine Toxoplasmosis in Sweden

Sera from 155 ewes representing 21 different sheep flocks from the central parts of Sweden were examined for the presence of antibodies to Toxoplasma gondii by the indirect fluorescent-antibody test. Seropositive animals were found in 14 flocks, which corresponded to 55 % of the tested sera. Animals from the same flock were with few exceptions either all positive or all negative. Some ewes with a history of abortion a few months before blood sampling showed high titers indicating causative correlation with toxoplasmosis. These are the first verified cases of ovine toxoplasmal abortions in Sweden.     

Chorio-Retinitis in Porcine Toxoplasmosis

Porcine toxoplasmosis generally occurs as a latent disease in adolescent and adult pigs, but now and then also manifests itself as a fatal congenital disease in piglets. It is known to occur in USA (Farrel et al. 1952), Germany (Becker 1954), Denmark (Momberg-Jørgensen 1956), Mexico (Varela et al. 1956), Japan (Sato et al. 1958), England (Harding et al. 1961) and Sweden (Hansen et al. to be published).