Oksanen Antti, Lavikainen Antti
Finnish Food Safety Authority Evira (FINPAR), Elektroniikkatie 3, FI-90590 Oulu, Finland.
Department of Bacteriology and Immunology (FINPAR), Haartman Institute, P.O. Box 21, FI-00014 University of Helsinki, Finland.
Vet Parasitol. 2015 Oct 30;213(3-4):182-6. doi: 10.1016/j.vetpar.2015.07.033. Epub 2015 Jul 31.
The Echinococcus granulosus complex (EG) is the causative agent of cystic echinococcosis (CE). Northern cervid Echinococcus was previously suggested to be the ancestor of the entire EG. During the last century, it was regarded to have three (or four) different, but often overlapping, transmission cycles in the circumpolar North: the original wolf-wild cervid (reindeer or elk)-cycle; the semi-synanthropic cycle involving sled and hunting dogs and wild cervids; and the synanthropic cycle involving herding dogs and semi-domesticated reindeer. Human infections mainly derived from the latter two cycles. In Fennoscandia, the synanthropic cycle has been eliminated during the last 50 years due to changes in reindeer husbandry methods; machinery making herding dogs largely redundant. Typical to human CE in the North has been the relatively benign nature of the disease compared with CE caused by E. granulosus sensu stricto. The metacestodes in humans and in the natural cervid hosts predominantly appear in the lungs. The causative agents have been identified as EG mitochondrial genotypes G8 and G10, now together with G6 (camel), G7 (pig) and G9 genotypes constituting the Echinococcus canadensis species. Based on recent findings in reindeer in Yakutia, G6 might also be recognised among cervid genotypes. The geographical distribution of both G8 and G10 is circumpolar, with G10 currently apparently more prevalent both in the Palearctic and Nearctic. Because of the disappearance of the working dog, E. canadensis in Fennoscandia is again highly dependent on the wolf, as it was before domestication of the dog. Pet and sled dogs, if their number further increases, may to a minor part participate in the life cycle. Human CE in the North was mostly diagnosed by mass chest tuberculosis radiography campaigns, which have been discontinued.
细粒棘球绦虫复合体(EG)是囊型棘球蚴病(CE)的病原体。北方鹿类棘球绦虫曾被认为是整个EG的祖先。在上个世纪,人们认为它在环北极地区有三个(或四个)不同但常常重叠的传播循环:原始的狼 - 野生鹿类(驯鹿或麋鹿)循环;涉及雪橇犬和猎犬以及野生鹿类的半共栖循环;以及涉及牧羊犬和半驯化驯鹿的共栖循环。人类感染主要源于后两个循环。在芬兰斯堪的纳维亚地区,由于驯鹿饲养方式的改变,共栖循环在过去50年中已被消除;机械设备使牧羊犬基本不再必要。与由狭义细粒棘球绦虫引起的CE相比,北方人类CE的典型特征是疾病性质相对温和。人类和天然鹿类宿主中的中绦期幼虫主要出现在肺部。病原体已被鉴定为EG线粒体基因型G8和G10,现在与G6(骆驼)、G7(猪)和G9基因型一起构成加拿大棘球绦虫物种。根据最近在雅库特驯鹿中的发现,G6在鹿类基因型中也可能被识别出来。G8和G10的地理分布都是环北极的,目前G10在古北区和新北区显然更为普遍。由于工作犬的消失,芬兰斯堪的纳维亚地区的加拿大棘球绦虫再次高度依赖狼,就像狗被驯化之前一样。宠物犬和雪橇犬如果数量进一步增加,可能会在较小程度上参与生命周期。北方的人类CE大多通过大规模胸部结核X线摄影筛查来诊断,而这些筛查活动已经停止。