Cargando…
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 sin...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Penerbit Universiti Sains Malaysia
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093768/ https://www.ncbi.nlm.nih.gov/pubmed/37065805 http://dx.doi.org/10.21315/tlsr2023.34.1.7 |
_version_ | 1785023665769807872 |
---|---|
author | Lau, Winnie Lik Sing Teng, Sing Tung Lim, Hong Chang Hii, Kieng Soon Leong, Sandric Chee Yew Leaw, Chui Pin Lim, Po Teen |
author_facet | Lau, Winnie Lik Sing Teng, Sing Tung Lim, Hong Chang Hii, Kieng Soon Leong, Sandric Chee Yew Leaw, Chui Pin Lim, Po Teen |
author_sort | Lau, Winnie Lik Sing |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10093768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Penerbit Universiti Sains Malaysia |
record_format | MEDLINE/PubMed |
spelling | pubmed-100937682023-04-13 Molecular Detection of the Harmful Raphidophyte Chattonella subsalsa Biecheler by Whole-Cell Fluorescence in-situ Hybridisation Assay Lau, Winnie Lik Sing Teng, Sing Tung Lim, Hong Chang Hii, Kieng Soon Leong, Sandric Chee Yew Leaw, Chui Pin Lim, Po Teen Trop Life Sci Res Article 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. Penerbit Universiti Sains Malaysia 2023-03 2023-03-31 /pmc/articles/PMC10093768/ /pubmed/37065805 http://dx.doi.org/10.21315/tlsr2023.34.1.7 Text en © Penerbit Universiti Sains Malaysia, 2023 https://creativecommons.org/licenses/by/4.0/This work is licensed under the terms of the Creative Commons Attribution (CC BY) (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Lau, Winnie Lik Sing Teng, Sing Tung Lim, Hong Chang Hii, Kieng Soon Leong, Sandric Chee Yew Leaw, Chui Pin Lim, Po Teen Molecular Detection of the Harmful Raphidophyte Chattonella subsalsa Biecheler by Whole-Cell Fluorescence in-situ Hybridisation Assay |
title | Molecular Detection of the Harmful Raphidophyte Chattonella subsalsa Biecheler by Whole-Cell Fluorescence in-situ Hybridisation Assay |
title_full | Molecular Detection of the Harmful Raphidophyte Chattonella subsalsa Biecheler by Whole-Cell Fluorescence in-situ Hybridisation Assay |
title_fullStr | Molecular Detection of the Harmful Raphidophyte Chattonella subsalsa Biecheler by Whole-Cell Fluorescence in-situ Hybridisation Assay |
title_full_unstemmed | Molecular Detection of the Harmful Raphidophyte Chattonella subsalsa Biecheler by Whole-Cell Fluorescence in-situ Hybridisation Assay |
title_short | Molecular Detection of the Harmful Raphidophyte Chattonella subsalsa Biecheler by Whole-Cell Fluorescence in-situ Hybridisation Assay |
title_sort | molecular detection of the harmful raphidophyte chattonella subsalsa biecheler by whole-cell fluorescence in-situ hybridisation assay |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093768/ https://www.ncbi.nlm.nih.gov/pubmed/37065805 http://dx.doi.org/10.21315/tlsr2023.34.1.7 |
work_keys_str_mv | AT lauwinnieliksing moleculardetectionoftheharmfulraphidophytechattonellasubsalsabiechelerbywholecellfluorescenceinsituhybridisationassay AT tengsingtung moleculardetectionoftheharmfulraphidophytechattonellasubsalsabiechelerbywholecellfluorescenceinsituhybridisationassay AT limhongchang moleculardetectionoftheharmfulraphidophytechattonellasubsalsabiechelerbywholecellfluorescenceinsituhybridisationassay AT hiikiengsoon moleculardetectionoftheharmfulraphidophytechattonellasubsalsabiechelerbywholecellfluorescenceinsituhybridisationassay AT leongsandriccheeyew moleculardetectionoftheharmfulraphidophytechattonellasubsalsabiechelerbywholecellfluorescenceinsituhybridisationassay AT leawchuipin moleculardetectionoftheharmfulraphidophytechattonellasubsalsabiechelerbywholecellfluorescenceinsituhybridisationassay AT limpoteen moleculardetectionoftheharmfulraphidophytechattonellasubsalsabiechelerbywholecellfluorescenceinsituhybridisationassay |