I found two cases of coccidiosis in Japan. Of rhese one died of this disease, while the other recovered. As regards the diagnosis my cases were very interesting. The clinical observations may briefly be described as follows:
The animal, one month old Holstein calf, was fed in the stall by an artificial suckling. It began to discharge the muddy faeces, and two days after it was found that they were mixed with blood and croupous pseudo-membrane. The faeces had a bad smell and were dark green or dark red in colour. Numerous oocysts were found in them.
The spores gradually decreased in mumber and became disappeared a weak after the commencement of the disease. From the post mortem examination it was found that no oocysts were contained in the contents of the whole intestine but the macrogametes were found to be scattered sporadically in the lumen of the Lieberkuhn's glands of colon.
The oocysts found in the stools were 11.9-34.0μ in length and 10.2-25.5μ in breadth. They were usually ovoid in shape but occasionally ellipsoid or spherical. The cystwall was colourless, but sometimes brownish in colour and double contoured; it was usually uniform in thickness and no micropyle was found. The cytoplasm which filled the cyst-cavity was colourless, or sometimes greenish or browhish yellow.
According to different temperature, as shown in the following table, the way of development of spore was varied.
At 37°C after 19 hours, sporoblasts 19.0% in number but no more developed and gradually destroyed.
At 30°C after 19 hours, sporoblasts 43.7% in number.
24 hours, sporocysts 63.6%
43 hours, sporocysts 75.0%
sporozoits 18.7%
oocysts 6.3%
67 hours, sporozoits 100%
At room temperature (21°C to 28°C)
after 19 hours, sporoblasts 3.1%
24 hours, sporoblasts 44.7%
43 hours, sporocysts 25.8%
67 hours, sporocysts 37.4%
sporozoits 35.0%
91 hours, sporozoits 83.0%
In the ice box (11°C to 15°C), spores did not develope until the 15th day.
after 35 days, sporocysts 88.7%
40 days, sporocysts 100%
The sporocysts were measured 17×6.8μ in the oocysts of 30.6×22.1μ, and 11.9×6.8μ in those of 25.5×18.7μ
For the experimental study two calves of one month old were used which were brought from healthy district. No spores were shown in the stools of these animals few days before the experiment. The calves were kept isolated, and the mature cysts cultured for 10-20 days under 30°C were given; and then the examination was made every day by Noller's table-salt method.
Calf A. 8 days after ingestion of the mature cysts, the calf excreted muddy faeces mixed with mucous membrane in which a few new oocysts were found. From the llth day no oocysts were detected.
Calf B. Five days after the ingestion of the cysts a few oocysts appeared in the feaces. They increased in number day after day till the 11th day, but not found after 16 days. The stools were quite normal in appearence from the beginning.
Calf C. 8 days after the ingestion of the mature spores the calf excreted muddy faeces mixed with mucous membrane in which a few cocysts appeared. They increased in number till 30 days, but nothing were found after 36 days.
Calf D. 2 days after the ingestion of the cysts a few oocysts appeared which increased in number day after day. On the 22th day the calf discharged bloody faeces in which numerous oocysts were found. Thye decreased in number from the next day. After 29 days no oocyst appeared in the faeces which changed to normal in appearence.
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