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首页> 外文期刊>Parasitology International >Morphological differences between larvae and in vitro-cultured adults of Anisakis simplex (sensu stricto) and Anisakis pegreffii (Nematoda: Anisakidae)
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Morphological differences between larvae and in vitro-cultured adults of Anisakis simplex (sensu stricto) and Anisakis pegreffii (Nematoda: Anisakidae)

机译:幼体和离体成年Anisakis simplex(Sensustricto)和Anisakis pegreffii(Nematoda:Anisakidae)的形态差异

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摘要

Proper identification of Anisakis species infecting host fishes is very important to both human health and fish disease diagnosis. The foremost problem in the identification of Anisakis larvae in fishes is that L3 larvae cannot be easily differentiated morphologically, especially between A. simplex (sensu stricto) (s.s.) (Rudolphi, 1809) and A. pegreffii Campana-Rouget et Biocca, 1955. Instead, molecular means such as allozyme, mitochondrial DNA (mtDNA) cox2 region and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analyses had been successfully used. In this study, morphological differences of L3 larvae collected from fishes and in vitro-cultured L4 larvae and adult A. simplex (s.s.) and A. pegreffii were evaluated. Anisakis larvae were collected from 7 different host fishes within Japan. Undamaged A. simplex (s.s.) and A. pegreffii collected from Oncorhynchus keta (Walbaum) and Scomber japonicus Houttuyn, respectively, were used for in vitro-culture in order to obtain L4 and adult stages. Species identification was confirmed by PCR-RFLP analysis of the ITS region (ITS1-5.8S-ITS2) of ribosomal DNA and by mtDNA cox2 gene sequencing. Results revealed that L3, L4 and adult stages of A. simplex (s.s.) and A. pegreffii are morphologically distinguishable based on ventriculus length, wherein the former has longer ventriculus (0.90-1.50 mm) than the latter (0.50-0.78 mm). For oesophagus/ventriculus ratio, these two species are distinguishable only during L4 and adult stages. Also, adult male A. simplex (s.s.) and A. pegreffii were found to be distinguishable by differences in the distribution pattern of the caudal papillae, particularly the 3rd pair of distal papillae.
机译:正确识别感染寄主鱼类的Anisakis物种对人类健康和鱼病诊断都非常重要。在鱼类中识别Anisakis幼虫的首要问题是L3幼虫在形态上不易区分,尤其是在A.simplex(sensu stricto)(ss)(Rudolphi,1809)和A. pegreffii Campana-Rouget et Biocca,1955之间。取而代之的是,已经成功使用了分子手段,例如同工酶,线粒体DNA(mtDNA)cox2区和聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析。在这项研究中,评估了从鱼类和体外培养的L4幼虫以及成年A. simplex(s.s.)和A. pegreffii收集的L3幼虫的形态学差异。 Anisakis幼虫是从日本的7种不同寄主鱼中收集的。分别从Oncorhynchus keta(Walbaum)和Scomber japonicus Houttuyn收集的未损坏的单纯曲霉和pegreffii进行体外培养,以获得L4和成年阶段。通过核糖体DNA ITS区(ITS1-5.8S-ITS2)的PCR-RFLP分析和mtDNA cox2基因测序,证实了物种鉴定。结果显示,根据脑室长度,在形态学上可区分单纯曲霉和小灵芝的L3,L4和成虫阶段,其中前者的脑室长(0.90-1.50 mm)比后者的脑室长(0.50-0.78 mm)。对于食道/脑室比率,这两个物种仅在L4和成年阶段才可区分。同样,发现成年雄性单纯曲霉(A.s.s.)和佩格氏曲霉(A.pegreffii)通过尾状乳头,尤其是第三对远端乳头的分布方式的差异是可区分的。

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