Suppr超能文献

用于检测条石鲷(Oplegnathus fasciatus)中岩田库道虫(粘孢子虫纲:多瓣虫目)的聚合酶链式反应(PCR)方法的开发

Development of PCR method for detecting Kudoa iwatai (Myxozoa: Multivalvulida) from rock bream Oplegnathus fasciatus.

作者信息

Jeon Chan-Hyeok, Do Jeung-Wan, Nam U-Hwa, Kim Wi-Sik, Kim Jeong-Ho

机构信息

East Coast Life Science Institute, Gangneung-Wonju National University, Gangneung, 25457, South Korea.

Department of Marine Bioscience, Gangneung-Wonju National University, Gangneung, 25457, South Korea.

出版信息

Parasitol Res. 2017 Feb;116(2):789-796. doi: 10.1007/s00436-016-5354-1. Epub 2016 Dec 23.

Abstract

We developed a PCR assay targeting the 28S rDNA of Kudoa iwatai (Multivalvulida: Myxozoa) and investigated the prevalence of infection in rock bream Oplegnathus fasciatus, which is commercially an important aquaculture species in Korea, with this assay. Detection limit of the PCR assay was 2.5 fg/μl with plasmid DNA and 8.6 × 10 spores/ml with purified spores, respectively. This PCR assay did not amplify DNA of other Kudoa species (Kudoa septempunctata, Kudoa lateolabracis, Kudoa thyrsites) tested. Sliced muscles of whole body from 318 rock bream (wild and cultured) were examined by this PCR assay and also with the naked eyes. All of the wild fish did not produce amplicons nor did harbor visible Kudoa cysts (0/70). Three of the cultured fish were PCR-positive and also harbored visible Kudoa cysts (3/248, 1.2%). The sequences of amplicons (574 bp) were 100% identical with those of the K. iwatai already registered in Genbank. When the visceral organs of these three fish were examined, visible cysts were not found, but one stomach sample was found to be PCR-positive. There was no difference in the prevalence of infection estimated by PCR assay and the presence of visible Kudoa cysts in our samples. This is thought to be because the development of K. iwatai is already completed and only mature Kudoa cysts existed in our samples.

摘要

我们开发了一种针对岩原鲤碘泡虫(多瓣虫纲:粘孢子虫)28S rDNA的PCR检测方法,并用该方法调查了条石鲷(韩国重要的商业养殖水产物种)的感染率。该PCR检测方法对质粒DNA的检测限为2.5 fg/μl,对纯化孢子的检测限为8.6×10个孢子/ml。该PCR检测方法未扩增所检测的其他碘泡虫物种(七斑碘泡虫、花鲈碘泡虫、三线碘泡虫)的DNA。用该PCR检测方法并通过肉眼检查了318条条石鲷(野生和养殖)的全身切片肌肉。所有野生鱼均未产生扩增子,也未发现可见的岩原鲤碘泡虫囊肿(0/70)。3条养殖鱼PCR检测呈阳性,且也有可见的岩原鲤碘泡虫囊肿(3/248,1.2%)。扩增子序列(574 bp)与Genbank中已登记的岩原鲤碘泡虫序列100%相同。检查这三条鱼的内脏器官时,未发现可见囊肿,但有一个胃样本PCR检测呈阳性。在我们的样本中,通过PCR检测估计的感染率与可见岩原鲤碘泡虫囊肿的存在情况之间没有差异。这被认为是因为岩原鲤碘泡虫的发育已经完成,我们的样本中仅存在成熟的岩原鲤碘泡虫囊肿。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验