Gibson W C, Dukes P, Gashumba J K
Department of Pathology, University of Bristol, School of Veterinary Science, Langford.
Parasitology. 1988 Aug;97 ( Pt 1):63-73. doi: 10.1017/s0031182000066749.
We have obtained 5 specific DNA probes for African trypanosomes of the subgenera Trypanozoon and Nannomonas. Each probe consists of one repeat unit of the major repetitive DNA (satellite DNA) of each species or intra-specific group. One probe hybridized with all members of subgenus Trypanozoon (except T. equiperdum which was not tested). In subgenus Nannomonas, one probe recognized T. simiae, but 3 probes were needed to identify all stocks of T. congolense available. Each of the 3 latter probes recognized trypanosomes from one of the 3 major groups of T. congolense previously defined by isoenzyme characterization, i.e. savannah, forest and Kenya coast types. As few as 100 trypanosomes could be unequivocally identified by dot blot hybridization and individual trypanosomes could be identified by in situ hybridization. We show how this simple methodology can be used in the field for the identification of immature and mature trypanosome infections in tsetse.
我们已经获得了针对锥虫亚属Trypanozoon和Nannomonas的非洲锥虫的5种特异性DNA探针。每个探针由每个物种或种内群体的主要重复DNA(卫星DNA)的一个重复单元组成。一种探针与Trypanozoon亚属的所有成员杂交(未测试的马媾疫锥虫除外)。在Nannomonas亚属中,一种探针识别猕猴锥虫,但需要3种探针来鉴定所有可用的刚果锥虫株。后3种探针中的每一种都识别先前通过同工酶特征定义的刚果锥虫3个主要群体之一的锥虫,即稀树草原型、森林型和肯尼亚海岸型。通过斑点印迹杂交,少至100个锥虫就能被明确鉴定,单个锥虫可通过原位杂交鉴定。我们展示了这种简单方法如何在野外用于鉴定采采蝇中未成熟和成熟的锥虫感染。