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基于18S核糖体DNA的PCR技术鉴定彭马基新帕拉变形虫,海水养殖鲑科鱼类阿米巴鳃病的病原体。

18S ribosomal DNA-based PCR identification of Neoparamoeba pemaquidensis, the agent of amoebic gill disease in sea-farmed salmonids.

作者信息

Wong Frank Y K, Carson Jeremy, Elliott Nicholas G

机构信息

Aquaculture and Biotechnology, CSIRO Marine Research, GPO Box 1538, Hobart 7001, Tasmania, Australia.

出版信息

Dis Aquat Organ. 2004 Jul 5;60(1):65-76. doi: 10.3354/dao060065.

Abstract

Neoparamoeba pemaquidensis is a parasomal amoeboid protozoan identified as the agent of amoebic gill disease (AGD) in Atlantic salmon Salmo salar reared in sea-pens in Tasmania, Australia, and coho salmon Oncorhynchus kisutch farmed on the west coast of the USA. Outbreaks of AGD caused by immunologically cross-reactive paramoebae have also been reported in sea-farmed salmonids in several other countries. Complete 18S rDNA sequences were determined for respective paramoebae isolated from infected gills of salmon from Tasmania and Ireland, and N. pemaquidensis isolates from the USA and UK, including representative free-living isolates. Alignments over 2110 bp revealed 98.1 to 99.0% sequence similarities among isolates, confirming that paramoebae implicated in AGD in geographically distant countries were homologous and belonged to the same species, N. pemaquidensis. The results supported previous findings that N. pemaquidensis exists as a widely distributed, amphizoic marine protozoan. Partial 18S rDNA sequences were obtained for the ultrastructurally similar species, N. aestuarina, and for the morphologically similar but non-parasomal amoeba Pseudoparamoeba pagei. N. aestuarina had 95.3 to 95.7% sequence similarities with N. pemaquidensis strains, which distinguished 2 closely related but separate species. Neoparamoeba spp. were not analogous to P. pagei or to other marine Gymnamoebia. We designed 4 oligonucleotide primers based on elucidated 18S rDNA sequences and applied them to single-step and nested 2-step PCR protocols developed to identify N. pemaquidensis to the exclusion of apparently closely related and non-related protistan taxa. Nested PCR was able to detect the AGD parasite from non-purified, culture-enriched net microfouling samples from Atlantic salmon sea-pens in Tasmania, and confirmed that N. pemaquidensis was also responsible for AGD in chinook salmon O. tshawytscha in New Zealand. Our sequence and PCR analyses have now shown that AGD affecting 3 different salmonid species farmed in 4 countries are associated with N. pemaquidensis. A species-specific diagnostic PCR provides for the first time, a highly specific detection and identification assay for N. pemaquidensis that will facilitate future ecological and epidemiological studies of AGD.

摘要

佩马奎迪新帕拉变形虫是一种寄生于鱼体的变形虫原生动物,被确定为澳大利亚塔斯马尼亚海水网箱养殖的大西洋鲑鱼以及美国西海岸养殖的银大麻哈鱼发生阿米巴鳃病(AGD)的病原体。在其他几个国家的海水养殖鲑科鱼类中,也报告了由免疫交叉反应性帕拉变形虫引起的AGD疫情。分别从塔斯马尼亚和爱尔兰感染鳃部的鲑鱼中分离出帕拉变形虫,以及从美国和英国分离出佩马奎迪新帕拉变形虫,包括代表性的自由生活分离株,测定了它们完整的18S rDNA序列。超过2110 bp的比对显示,分离株之间的序列相似性为98.1%至99.0%,证实了在地理上相距遥远的国家中与AGD有关的帕拉变形虫是同源的,属于同一物种,即佩马奎迪新帕拉变形虫。这些结果支持了先前的研究发现,即佩马奎迪新帕拉变形虫是一种广泛分布的兼性海洋原生动物。获得了超微结构相似的物种河口新帕拉变形虫以及形态相似但非寄生于鱼体的变形虫佩奇假帕拉变形虫的部分18S rDNA序列。河口新帕拉变形虫与佩马奎迪新帕拉变形虫菌株的序列相似性为95.3%至95.7%,这区分了两个密切相关但独立的物种。新帕拉变形虫属与佩奇假帕拉变形虫或其他海洋裸变形虫不同。我们根据已阐明的18S rDNA序列设计了4种寡核苷酸引物,并将其应用于为鉴定佩马奎迪新帕拉变形虫而开发的单步和巢式两步PCR方案中,以排除明显密切相关和不相关的原生生物类群。巢式PCR能够从塔斯马尼亚大西洋鲑鱼海水网箱中未经纯化、经培养富集的网微污损样本中检测到AGD寄生虫,并证实佩马奎迪新帕拉变形虫也是新西兰奇努克鲑鱼发生AGD的病原体。我们的序列和PCR分析现已表明,影响4个国家养殖的3种不同鲑科鱼类的AGD与佩马奎迪新帕拉变形虫有关。一种物种特异性诊断PCR首次为佩马奎迪新帕拉变形虫提供了一种高度特异性的检测和鉴定方法,这将有助于未来对AGD的生态学和流行病学研究。

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