Masiga Daniel K, Ndung'u Kariuki, Tweedie Alison, Tait Andrew, Turner C Michael R
Division of Infection and Immunity, IBLS, Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow G12 8TA, UK.
Exp Parasitol. 2006 Nov;114(3):147-53. doi: 10.1016/j.exppara.2006.03.002. Epub 2006 Apr 19.
We compared two methods to generate polymorphic markers to investigate the population genetics of Trypanosoma evansi; random amplified polymorphic DNA (RAPD) and amplified restriction fragment length polymorphism (AFLP) analyses. AFLP accessed many more polymorphisms than RAPD. Cluster analysis of the AFLP data showed that 12 T.evansi isolates were very similar ('type A') whereas 2 isolates differed substantially ('type B'). Type A isolates have been generally regarded as genetically identical but AFLP analysis was able to identify multiple differences between them and split the type A T. evansi isolates into two distinct clades.
我们比较了两种用于生成多态性标记以研究伊氏锥虫群体遗传学的方法;随机扩增多态性DNA(RAPD)分析和扩增片段长度多态性(AFLP)分析。AFLP检测到的多态性比RAPD多得多。对AFLP数据的聚类分析表明,12株伊氏锥虫分离株非常相似(“A型”),而2株分离株有显著差异(“B型”)。A型分离株通常被认为在基因上是相同的,但AFLP分析能够识别它们之间的多个差异,并将A型伊氏锥虫分离株分为两个不同的进化枝。