Maraghi S, Wallbanks K R, Molyneux D H
Department of Medical Parasitology and Mycology, Medical School, University of Medical Sciences, Ahwaz, Iran.
Parasitol Res. 1995;81(8):693-5. doi: 10.1007/BF00931848.
The rodents Microtus agrestis, Clethrionomys glareolus, Apodemus sylvaticus and white BK rats were given either a single intraperitoneal (i.p.) injection, an intragastric (i.g.) inoculation or an oral (p.o.) inoculation of the culture forms, including metacyclic trypomastigotes, of Trypanosoma microti, T. evotomys, T. grosi and T. lewisi, respectively. Similar levels of parasitaemia were produced by each of the three routes of infection, although the prepatent period was 3-5 days shorter in the case of the i.p.-injected animals. The oral inoculation of blood from mice infected with T. musculi into uninfected mice (outbred) and from rats infected with T. lewisi into uninfected BK rats produced parasitaemia after 6-8 days. This is the first report of the oral and i.g. transmission of T. microti, T. evotomys and T. grosi into their specific homologous hosts.
分别给田鼠、棕背䶄、林姬鼠和白色BK大鼠腹腔内单次注射、灌胃接种或口服接种微小巴贝斯虫、伊氏巴贝斯虫、格氏巴贝斯虫和刘易斯锥虫的培养形式,包括循环后期锥鞭毛体。三种感染途径产生的寄生虫血症水平相似,不过腹腔注射动物的潜伏期缩短3 - 5天。将感染鼠巴贝斯虫的小鼠血液口服接种到未感染的(远交)小鼠体内,以及将感染刘易斯锥虫的大鼠血液口服接种到未感染的BK大鼠体内,6 - 8天后产生了寄生虫血症。这是关于微小巴贝斯虫、伊氏巴贝斯虫和格氏巴贝斯虫经口服和灌胃传播到其特定同源宿主的首次报道。