Southgate V R, Brown D S, Warlow A, Knowles R J, Jones A
Department of Zoology, British Museum (Natural History), South Kensington, London, UK.
Parasitol Res. 1989;75(5):381-91. doi: 10.1007/BF00931134.
A total of 480 snails were collected from 3 habitats on the Mau Escarpment, Kenya, and were identified as Bulinus tropicus. Of the 351 snails examined alive in London, 75 were infected with Calicophoron microbothrium, 39 with C. microbothrium and Schistosoma bovis, 1 with S. bovis, 24 with other species of trematodes and 212 were uninfected. Examination of digestive glands of B. tropicus either uninfected or infected with both C. microbothrium and S. bovis demonstrated that it is possible to differentiate between parasite and host enzyme activity using glucose phosphate isomerase. However, malate dehydrogenase enables a much clearer differentiation between the enzyme activity of the schistosome and that of the amphistome. Laboratory snail infection experiments demonstrated that it is possible successfully to infect B. tropicus with S. bovis if the snails have previously been exposed to miracidia of C. microbothrium.
从肯尼亚莫阿悬崖的3个栖息地共采集了480只蜗牛,鉴定为热带泡螺。在伦敦对351只活蜗牛进行检查,其中75只感染了微小杯殖吸虫,39只感染了微小杯殖吸虫和牛血吸虫,1只感染了牛血吸虫,24只感染了其他种类的吸虫,212只未感染。对未感染或同时感染微小杯殖吸虫和牛血吸虫的热带泡螺消化腺进行检查表明,利用磷酸葡萄糖异构酶可以区分寄生虫和宿主的酶活性。然而,苹果酸脱氢酶能更清楚地区分血吸虫和双口吸虫的酶活性。实验室蜗牛感染实验表明,如果蜗牛先前已接触过微小杯殖吸虫的毛蚴,就有可能成功地用牛血吸虫感染热带泡螺。