Douglas R J, Sundermann C A, Perry L D, Douglas T S, Lindsay D S
Department of Zoology and Wildlife Science, Alabama Agricultural Experiment Station, Auburn University 36849.
Vet Parasitol. 1993 Oct;50(1-2):55-67. doi: 10.1016/0304-4017(93)90007-a.
Four crossbred pigs (Sus scrofa) were inoculated orally with Caryospora bigenetica oocysts derived from snake and mouse feces, and with C. bigenetica infected mouse tissue. One pig also was given i.m. injections of methylprednisolone acetate. All four pigs displayed clinical signs including erythema, edema, and lethargy. Caryocysts were observed histologically in numerous tissues including ear, tongue, jowl, shoulder, loin, intercostal, ham, hock, and feet. The four pigs each were butchered into six commercial cuts: shoulder, loin, side, ham, hock, and feet. Raw 10 g samples from each cut were bioassayed by pepsin digestion and s.c. inoculation into 12 Swiss-Webster mice (Mus musculus) and 12 cotton rats (Sigmodon hispidus). Seventeen of 24 mice and cotton rats exhibited clinical signs and C. bigenetica tissue infections. Remaining portions of the six commercial cuts were temperature or saline treated, and 10 g samples were bioassayed in 16 mice and 12 cotton rats. No clinical sign or tissue infection was observed in these animals. Our study presents evidence that swine can be infected with C. bigenetica by ingesting oocysts present in snake feces or mouse feces (following inoculation of mice with snake-derived oocysts) or by ingesting C. bigenetica infected rodent tissue, that endogenously produced C. bigenetica oocysts are not excreted in the feces of swine, and that C. bigenetica in pork can be rendered noninfective by freezing at -20 degrees C (-4 degrees F) for 21 days, frying at 84 degrees C (183 degrees F) for 17 min, microwaving at 88 degrees C (190 degrees F) for 17 min, grilling at 82 degrees C (180 degrees F) for 48 min, baking at 95 degrees C (203 degrees F) for 230 min, boiling at 100 degrees C (212 degrees F) for 60 min, or by curing at 4 degrees C (39 degrees F) for 20 days.
四只杂交猪(野猪)经口接种了源自蛇和小鼠粪便的双基因球虫孢囊以及感染双基因球虫的小鼠组织。其中一只猪还接受了醋酸甲泼尼龙的肌肉注射。所有四只猪均表现出包括红斑、水肿和嗜睡在内的临床症状。在包括耳朵、舌头、颌、肩部、腰部、肋间、火腿、跗关节和足部在内的许多组织中通过组织学观察到了球囊。这四只猪分别被分割成六种商业切块:肩部、腰部、肋腹、火腿、跗关节和足部。从每个切块取10克生样本,通过胃蛋白酶消化和皮下接种到12只瑞士韦伯斯特小鼠(小家鼠)和12只棉鼠(刚毛囊鼠)中进行生物测定。24只小鼠和棉鼠中有17只表现出临床症状和双基因球虫组织感染。对六种商业切块的剩余部分进行了温度或盐水处理,并在16只小鼠和12只棉鼠中对10克样本进行了生物测定。在这些动物中未观察到临床症状或组织感染。我们的研究提供了证据,表明猪可通过摄入蛇粪便或小鼠粪便中的卵囊(在用源自蛇的卵囊接种小鼠后)或摄入感染双基因球虫的啮齿动物组织而感染双基因球虫,内源性产生的双基因球虫卵囊不会在猪的粪便中排出,并且猪肉中的双基因球虫可通过在-20℃(-4℉)冷冻21天、在84℃(183℉)油炸17分钟、在88℃(190℉)微波处理17分钟、在82℃(180℉)烧烤48分钟、在95℃(203℉)烘烤230分钟、在100℃(212℉)煮沸60分钟或在4℃(39℉)腌制20天而变得无传染性。