Abe Niichiro
Department of Microbiology, Osaka City Institute of Public Health and Environmental Sciences, Tennoji-ku, Osaka 543-0026, Japan.
Parasitol Res. 2008 Apr;102(5):1073-5. doi: 10.1007/s00436-008-0886-7. Epub 2008 Feb 1.
The fish-borne zoonotic nematode, Anisakis simplex, is not a single specie but a complex composed of three sibling species, A. simplex sensu stricto, Anisakis pegreffii, and A. simplex C. Discrimination among these sibling species have been performed by polymerase chain reaction (PCR)-restriction fragment length polymorphism or sequencing analysis of the internal transcribed spacer (ITS) region of ribosomal DNA (rDNA). In the present study, PCR-sequence-specific primers were applied for the discrimination of these parasites. Based on the sequence differences among A. simplex complex at the ITS region of rDNA, forward primer ASF1 that is expected to be specific to A. pegreffii was newly developed. The specific fragment was amplified in only A. pegreffii by PCR with ASF1, but not quite in A. simplex s. str., Anisakis physeteris, Pseudoterranova decipiens, and Contracaecum osculatum. This result suggests that PCR using the forward primer ASF1 might be applicable for the discrimination of A. simplex complex.
食源性人畜共患线虫简单异尖线虫并非单一物种,而是由三个姊妹种组成的复合体,即狭义简单异尖线虫、佩氏异尖线虫和简单异尖线虫C型。这些姊妹种之间的鉴别一直通过核糖体DNA(rDNA)内转录间隔区(ITS)的聚合酶链反应(PCR)-限制性片段长度多态性或测序分析来进行。在本研究中,应用PCR序列特异性引物来鉴别这些寄生虫。基于rDNA ITS区域简单异尖线虫复合体之间的序列差异,新开发了预期对佩氏异尖线虫具有特异性的正向引物ASF1。通过使用ASF1进行PCR,仅在佩氏异尖线虫中扩增出特异性片段,而在狭义简单异尖线虫、抹香鲸异尖线虫、欺骗新蛔线虫和吻状对盲囊线虫中则未扩增出。这一结果表明,使用正向引物ASF1进行PCR可能适用于简单异尖线虫复合体的鉴别。