Lindsay David S, Collins Marina V, Mitchell Sheila M, Cole Rebecca A, Flick George J, Wetch Carly N, Lindquist Alan, Dubey J P
Department of Biomedical Sciences and Pathobiology, 1410 Prices Fork Road, Virginia Tech, Blacksburg, VA 24061, USA.
J Eukaryot Microbiol. 2003;50 Suppl:687-8. doi: 10.1111/j.1550-7408.2003.tb00688.x.
We have been collaborating since 1992 in studies on southern sea otters (Enhydra lutris nereis) as part of a program to define factors, which may be responsible for limiting the growth of the southern sea otter population. We previously demonstrated Toxoplasma gondii in sea otters. We postulated that cat feces containing oocysts could be entering the marine environment through storm run-off or through municipal sewage since cat feces are often disposed down toilets by cat owners. The present study examined the sporulation of T. gondii oocysts in seawater and the survival of sporulated oocysts in seawater. Unsporulated oocysts were placed in 15 ppt artificial seawater, 32 ppt artificial seawater or 2% sulfuric acid (positive control) at 24 C in an incubator. Samples were examined daily for 3 days and development monitored by counting 100 oocysts from each sample. From 75 to 80% of the oocysts were sporulated by 3 days post-inoculation under all treatment conditions. Groups of 2 mice were fed 10,000 oocysts each from each of the 3 treatment groups. All inoculated mice developed toxoplasmosis indicating that oocysts were capable of sporulating in seawater. Survival of sporulated oocysts was examined by placing sporulated T. gondii oocysts in 15 ppt seawater at room temperature 22-24 C (RT) or in a refrigerator kept at 4 C. Mice fed oocysts that had been stored at 4C or RT for 6 months became infected. These results indicate that T. gondii oocysts can sporulate and remain viable in seawater for several months.
自1992年以来,我们一直合作开展关于南海獭(Enhydra lutris nereis)的研究,作为确定可能限制南海獭种群增长因素项目的一部分。我们之前在海獭体内发现了刚地弓形虫。我们推测,含有卵囊的猫粪可能通过暴雨径流或城市污水进入海洋环境,因为猫主人经常将猫粪冲进马桶。本研究检测了刚地弓形虫卵囊在海水中的孢子化情况以及孢子化卵囊在海水中的存活情况。未孢子化的卵囊置于15ppt人工海水、32ppt人工海水或2%硫酸(阳性对照)中,于24℃在培养箱中培养。每天对样本进行检测,持续3天,并通过对每个样本的100个卵囊计数来监测发育情况。在所有处理条件下,接种后3天,75%至80%的卵囊孢子化。从3个处理组中的每组分别选取2只小鼠,每只小鼠喂食10000个卵囊。所有接种的小鼠都患上了弓形虫病,表明卵囊能够在海水中孢子化。通过将孢子化的刚地弓形虫卵囊置于室温22 - 24℃(RT)的15ppt海水中或置于4℃的冰箱中,检测孢子化卵囊的存活情况。喂食在4℃或室温下储存6个月的卵囊的小鼠被感染。这些结果表明,刚地弓形虫卵囊能够在海水中孢子化并存活数月。