Pathology and Parasitology Department, Faculty of Veterinary Medicine, Damanhour University, Damanhour, Egypt,
Parasitol Res. 2013 Oct;112(10):3557-60. doi: 10.1007/s00436-013-3539-4. Epub 2013 Aug 21.
The genomic DNA was extracted from nematode parasites, Heterakis gallinae from specific host, native chickens. The polymerase chain reaction (PCR) was applied to make amplification of the DNA content that aids in the further studies. The primer was used in the PCR reactions that have the following sequences: forward (5'-GTTTCCGTAGGTGAACCTGC-3') and reverse (5'-ATATGCTTAAGTTCAGCGGGT-3'). It gave total amplified fragment markers at 914 bp. The gene sequences obtained from Egyptian H. gallinae was to make phylogenetic relationships of Egyptian H. gallinae with other nematodes on the database of an accession number (AJ876757), showing that it was nearly similar to Heterakis gallinarum.
从特定宿主本地鸡的寄生虫禽异刺线虫中提取基因组 DNA。应用聚合酶链反应(PCR)对 DNA 含量进行扩增,以进一步研究。PCR 反应中使用的引物序列如下:正向(5'-GTTTCCGTAGGTGAACCTGC-3')和反向(5'-ATATGCTTAAGTTCAGCGGGT-3')。它产生了 914bp 的总扩增片段标记。从埃及禽异刺线虫获得的基因序列用于在数据库中建立埃及禽异刺线虫与其他线虫的系统发育关系(登录号 AJ876757),表明它与禽异刺线虫非常相似。