Quantitative real-time PCR detection of a harmful unarmoured dinoflagellate, Karlodinium australe (Dinophyceae)

We investigated a harmful algal bloom (HAB) associated with the massive fish kills in Johor Strait, Malaysia, which recurred a year after the first incident in 2014. This incident has urged for the need to have a rapid and precise method in HAB monitoring. In this study, we develop a SYBR green-...

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Main Authors: Nyuk, Fong Kon, Lau, Winnie L.S., Kieng, Soon Hii, Ing, Kuo Law, Sing, Tung Teng, Hong, Chang Lim, Takahashi, Kazuya, Gu, Haifeng, Po, Teen Lim, Chui, Pin Leaw
Format: Article
Language:English
Published: Blackwell Publishing Ltd 2017
Subjects:
Online Access:http://ir.unimas.my/id/eprint/17074/
http://ir.unimas.my/id/eprint/17074/1/Quantitative%20real-time%20PCR%20detection%20of%20a%20harmful%20%28abstract%29.pdf
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author Nyuk, Fong Kon
Lau, Winnie L.S.
Kieng, Soon Hii
Ing, Kuo Law
Sing, Tung Teng
Hong, Chang Lim
Takahashi, Kazuya
Gu, Haifeng
Po, Teen Lim
Chui, Pin Leaw
author_facet Nyuk, Fong Kon
Lau, Winnie L.S.
Kieng, Soon Hii
Ing, Kuo Law
Sing, Tung Teng
Hong, Chang Lim
Takahashi, Kazuya
Gu, Haifeng
Po, Teen Lim
Chui, Pin Leaw
author_sort Nyuk, Fong Kon
building UNIMAS Institutional Repository
collection Online Access
description We investigated a harmful algal bloom (HAB) associated with the massive fish kills in Johor Strait, Malaysia, which recurred a year after the first incident in 2014. This incident has urged for the need to have a rapid and precise method in HAB monitoring. In this study, we develop a SYBR green-based realtime PCR (qPCR) to detect the culpable dinoflagellate species, Karlodinium australe. Species-specific qPCR primers were designed in the gene region of the second internal transcribed spacer of the ribosomal RNA gene (rDNA). The species specificity of the primers designed was evaluated by screening on the non-target species (Karlodinium veneficum, Takayama spp., and Karenia spp.) and no cross-detection was observed. The extractable gene copies per cell of K. australe determined in this study were 19 998 � 505 (P < 0.0001). Estimation of cell densities by qPCR in the experimental spiked samples showed high correlation with data determined microscopically (R2 = 0.93). Using the qPCR assay developed in this study, we successfully detected the 2015 bloom species as K. australe. Single-cell PCR and rDNA sequencing from the field samples further confirmed the finding. With the sensitivity as low as five cells, the qPCR assay developed in this study could effectively and rapidly detect cells of K. australe in the environmental samples for monitoring purpose.
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spelling unimas-170742017-10-13T00:35:06Z http://ir.unimas.my/id/eprint/17074/ Quantitative real-time PCR detection of a harmful unarmoured dinoflagellate, Karlodinium australe (Dinophyceae) Nyuk, Fong Kon Lau, Winnie L.S. Kieng, Soon Hii Ing, Kuo Law Sing, Tung Teng Hong, Chang Lim Takahashi, Kazuya Gu, Haifeng Po, Teen Lim Chui, Pin Leaw SH Aquaculture. Fisheries. Angling We investigated a harmful algal bloom (HAB) associated with the massive fish kills in Johor Strait, Malaysia, which recurred a year after the first incident in 2014. This incident has urged for the need to have a rapid and precise method in HAB monitoring. In this study, we develop a SYBR green-based realtime PCR (qPCR) to detect the culpable dinoflagellate species, Karlodinium australe. Species-specific qPCR primers were designed in the gene region of the second internal transcribed spacer of the ribosomal RNA gene (rDNA). The species specificity of the primers designed was evaluated by screening on the non-target species (Karlodinium veneficum, Takayama spp., and Karenia spp.) and no cross-detection was observed. The extractable gene copies per cell of K. australe determined in this study were 19 998 � 505 (P < 0.0001). Estimation of cell densities by qPCR in the experimental spiked samples showed high correlation with data determined microscopically (R2 = 0.93). Using the qPCR assay developed in this study, we successfully detected the 2015 bloom species as K. australe. Single-cell PCR and rDNA sequencing from the field samples further confirmed the finding. With the sensitivity as low as five cells, the qPCR assay developed in this study could effectively and rapidly detect cells of K. australe in the environmental samples for monitoring purpose. Blackwell Publishing Ltd 2017 Article PeerReviewed text en http://ir.unimas.my/id/eprint/17074/1/Quantitative%20real-time%20PCR%20detection%20of%20a%20harmful%20%28abstract%29.pdf Nyuk, Fong Kon and Lau, Winnie L.S. and Kieng, Soon Hii and Ing, Kuo Law and Sing, Tung Teng and Hong, Chang Lim and Takahashi, Kazuya and Gu, Haifeng and Po, Teen Lim and Chui, Pin Leaw (2017) Quantitative real-time PCR detection of a harmful unarmoured dinoflagellate, Karlodinium australe (Dinophyceae). Phycological Research, 65 (4). pp. 291-298. ISSN 1322-0829 http://onlinelibrary.wiley.com/doi/10.1111/pre.12186/full doi: 10.1111/pre.12186
spellingShingle SH Aquaculture. Fisheries. Angling
Nyuk, Fong Kon
Lau, Winnie L.S.
Kieng, Soon Hii
Ing, Kuo Law
Sing, Tung Teng
Hong, Chang Lim
Takahashi, Kazuya
Gu, Haifeng
Po, Teen Lim
Chui, Pin Leaw
Quantitative real-time PCR detection of a harmful unarmoured dinoflagellate, Karlodinium australe (Dinophyceae)
title Quantitative real-time PCR detection of a harmful unarmoured dinoflagellate, Karlodinium australe (Dinophyceae)
title_full Quantitative real-time PCR detection of a harmful unarmoured dinoflagellate, Karlodinium australe (Dinophyceae)
title_fullStr Quantitative real-time PCR detection of a harmful unarmoured dinoflagellate, Karlodinium australe (Dinophyceae)
title_full_unstemmed Quantitative real-time PCR detection of a harmful unarmoured dinoflagellate, Karlodinium australe (Dinophyceae)
title_short Quantitative real-time PCR detection of a harmful unarmoured dinoflagellate, Karlodinium australe (Dinophyceae)
title_sort quantitative real-time pcr detection of a harmful unarmoured dinoflagellate, karlodinium australe (dinophyceae)
topic SH Aquaculture. Fisheries. Angling
url http://ir.unimas.my/id/eprint/17074/
http://ir.unimas.my/id/eprint/17074/
http://ir.unimas.my/id/eprint/17074/
http://ir.unimas.my/id/eprint/17074/1/Quantitative%20real-time%20PCR%20detection%20of%20a%20harmful%20%28abstract%29.pdf