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通过原位杂交检测金头鲷细胞核内微孢子虫嗜核肠孢虫

Detection of the intranuclear microsporidian Enterospora nucleophila in gilthead sea bream by in situ hybridization.

作者信息

Ahmed Nahla Hossameldin, Caffara Monica, Sitjà-Bobadilla Ariadna, Fioravanti Maria Letizia, Mazzone Angelica, Aboulezz Abbass Sayed, Metwally Asmaa Mohamed, Omar Mosaab Adl-Eldin, Palenzuela Oswaldo R

机构信息

Institute of Aquaculture "Torre de la Sal" (IATS-CSIC), Castellón, Spain.

National Institute of Oceanography and Fisheries (NIOF), Hurghada, Egypt.

出版信息

J Fish Dis. 2019 Jun;42(6):809-815. doi: 10.1111/jfd.12993. Epub 2019 Apr 10.

DOI:10.1111/jfd.12993
PMID:30968978
Abstract

Enterospora nucleophila is an intranuclear microsporidian responsible for emaciative microsporidiosis of gilthead sea bream (GSB). Its minute size and cryptic nature make it easily misdiagnosed. An in situ hybridization (ISH) technique based on antisense oligonucleotide probes specific for the parasite was developed and used in clinically infected GSB in combination with calcofluor white stain (CW) and other histopathological techniques. The ISH method was found to label very conspicuously the cells containing parasite stages, with the signal concentrating in merogonial and sporogonial plasmodia within the infected cell nuclei. Comparison with CW demonstrated limited ISH signal in cells containing mature spores, which was attributed mostly to the scarcity of probe targets present in these stages. Although spores were detected in other organs of the digestive system as well as in the peripheral blood, proliferative stages or parasite reservoirs were not found in this work outside the intestines. The study demonstrated a frequent disassociation between the presence of abundant spores and the intensity of the infections as determined by the parasite activity. The ISH allows confirmatory diagnosis of GSB microsporidiosis and estimation of infection intensity and will be a valuable tool for a more precise determination of parasite dissemination pathways and pathogeny mechanisms.

摘要

嗜核肠孢虫是一种核内微孢子虫,可导致金头鲷的消瘦性微孢子虫病。其微小的尺寸和隐匿的特性使其容易被误诊。基于针对该寄生虫的反义寡核苷酸探针开发了一种原位杂交(ISH)技术,并将其与荧光增白剂(CW)及其他组织病理学技术结合应用于临床感染的金头鲷。结果发现,ISH方法能非常显著地标记含有寄生虫阶段的细胞,信号集中在感染细胞核内的裂殖体和孢子体中。与CW的比较表明,含有成熟孢子的细胞中ISH信号有限,这主要归因于这些阶段存在的探针靶点稀少。尽管在消化系统的其他器官以及外周血中检测到了孢子,但在本研究中,肠道外未发现增殖阶段或寄生虫储存库。该研究表明,大量孢子的存在与由寄生虫活性确定的感染强度之间经常存在脱节。ISH可用于金头鲷微孢子虫病的确诊和感染强度的评估,将成为更精确确定寄生虫传播途径和致病机制的有价值工具。

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