用全细胞荧光原位杂交法检测有害沙顿菌的分子结构。

IF 1.1 Q3 BIOLOGY
Winnie Lik Sing Lau, Sing Tung Teng, Hong Chang Lim, Kieng Soon Hii, Sandric Chee Yew Leong, Chui Pin Leaw, Po Teen Lim
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引用次数: 0

摘要

chatonella属(Raphidophyceae)是一组常见于沿海水域的海洋原生生物。其中一些被称为有害微藻,它们会形成有毒的水华,并在鱼类养殖中造成大量鱼类死亡。在马来西亚,自20世纪80年代以来,在柔佛海峡就有查顿菌大量繁殖的记录。本研究从海峡中分离出两株查顿菌,形态学检查显示其特征与萨尔下查顿菌相似。分子鉴定进一步证实了该物种为C. subsalsa。为了准确检测环境中隐球菌的细胞,建立了一种全细胞荧光原位杂交(FISH)方法。基于核糖体DNA (rDNA)的大亚基(LSU)和内部转录间隔区2 (ITS2)的核苷酸序列,用计算机设计了物种特异性寡核苷酸探针。根据杂交效率和探针参数选择LSU-rRNA和ITS2-rDNA的最佳候选特征区。将探针合成为生物素化探针,并用FISH (FISH- tsa)进行酪酰胺信号放大检测。结果表明探针对靶细胞具有特异性。FISH-TSA已被证明是一种潜在的环境有害藻类检测工具,可应用于有害藻类监测项目。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular Detection of the Harmful Raphidophyte <i>Chattonella subsalsa</i> Biecheler by Whole-Cell Fluorescence <i>in-situ</i> Hybridisation Assay.

Molecular Detection of the Harmful Raphidophyte <i>Chattonella subsalsa</i> Biecheler by Whole-Cell Fluorescence <i>in-situ</i> Hybridisation Assay.

Molecular Detection of the Harmful Raphidophyte <i>Chattonella subsalsa</i> Biecheler by Whole-Cell Fluorescence <i>in-situ</i> Hybridisation Assay.

Molecular Detection of the Harmful Raphidophyte Chattonella subsalsa Biecheler by Whole-Cell Fluorescence in-situ Hybridisation Assay.

Species of the genus Chattonella (Raphidophyceae) are a group of marine protists that are commonly found in coastal waters. Some are known as harmful microalgae that form noxious blooms and cause massive fish mortality in finfish aquaculture. In Malaysia, blooms of Chattonella have been recorded since the 1980s in the Johor Strait. In this study, two strains of Chattonella were established from the strait, and morphological examination revealed characteristics resembling Chattonella subsalsa. The molecular characterization further confirmed the species' identity as C. subsalsa. To precisely detect the cells of C. subsalsa in the environment, a whole-cell fluorescence in-situ hybridisation (FISH) assay was developed. The species-specific oligonucleotide probes were designed in silico based on the nucleotide sequences of the large subunit (LSU) and internal transcribed spacer 2 (ITS2) of the ribosomal DNA (rDNA). The best candidate signature regions in the LSU-rRNA and ITS2-rDNA were selected based on hybridisation efficiency and probe parameters. The probes were synthesised as biotinylated probes and tested by tyramide signal amplification with FISH (FISH-TSA). The results showed the specificity of the probes toward the target cells. FISH-TSA has been proven to be a potential tool in the detection of harmful algae in the environment and could be applied to the harmful algal monitoring program.

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来源期刊
CiteScore
2.60
自引率
0.00%
发文量
40
审稿时长
20 weeks
期刊介绍: Tropical Life Sciences Research (TLSR) formerly known as Journal of Bioscience seeks to publish relevant ideas and knowledge addressing vital life sciences issues in the tropical region. The Journal’s scope is interdisciplinary in nature and covers any aspects related to issues on life sciences especially from the field of biochemistry, microbiology, biotechnology and animal, plant, environmental, biomedical and pharmaceutical sciences. TLSR practices double blind peer review system to ensure and maintain the good quality of articles published in this journal. Two issues are published annually in printed and electronic form. TLSR also accepts review articles, experimental papers and short communications. The Chief Editor would like to invite researchers to use this journal as a mean to rapidly promote their research findings.
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