A real-time PCR method for rapid detection of Gymnodinium sanguineum

For detecting the harmful algal bloom (HAB) species sensitively and rapidly, Gymnodinium sanguineum was taken as the object, and the rapid detection method- RFQ-PCR (real-time fluorescent quantitative polymerase chain reaction) technique was applied to the HAB species detection. Firstly, gene specif...

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Main Authors: HE Shan-ying, YU Zhi-gang
Format: Article
Language:English
Published: Zhejiang University Press 2009-03-01
Series:浙江大学学报. 农业与生命科学版
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Online Access:https://www.academax.com/doi/10.3785/j.issn.1008-9209.2009.02.001
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author HE Shan-ying
YU Zhi-gang
author_facet HE Shan-ying
YU Zhi-gang
author_sort HE Shan-ying
collection DOAJ
description For detecting the harmful algal bloom (HAB) species sensitively and rapidly, Gymnodinium sanguineum was taken as the object, and the rapid detection method- RFQ-PCR (real-time fluorescent quantitative polymerase chain reaction) technique was applied to the HAB species detection. Firstly, gene specific primers and a TaqMan DNA probe were designed based on the sequence of 18S rDNA cloned from G. sanguineum. Then, using the primers and probe combination, a RFQ-PCR method was developed for quantitative detection of G. sanguineum, a harmful algae bloom species. The RFQ-PCR assay data showed good agreement with traditional microscope counting methods, suggesting that RFQ-PCR may be a useful method for detecting G. sanguineum. The detection threshold tested was much lower than that of G. sanguineum HAB, so this technique will be useful for forecasting and preventing G. sanguineum HAB.
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institution Kabale University
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record_format Article
series 浙江大学学报. 农业与生命科学版
spelling doaj-art-837493e8e3824a1bbda962b798c842e52025-08-20T03:58:17ZengZhejiang University Press浙江大学学报. 农业与生命科学版1008-92092097-51552009-03-013511912610.3785/j.issn.1008-9209.2009.02.00110089209A real-time PCR method for rapid detection of Gymnodinium sanguineumHE Shan-yingYU Zhi-gangFor detecting the harmful algal bloom (HAB) species sensitively and rapidly, Gymnodinium sanguineum was taken as the object, and the rapid detection method- RFQ-PCR (real-time fluorescent quantitative polymerase chain reaction) technique was applied to the HAB species detection. Firstly, gene specific primers and a TaqMan DNA probe were designed based on the sequence of 18S rDNA cloned from G. sanguineum. Then, using the primers and probe combination, a RFQ-PCR method was developed for quantitative detection of G. sanguineum, a harmful algae bloom species. The RFQ-PCR assay data showed good agreement with traditional microscope counting methods, suggesting that RFQ-PCR may be a useful method for detecting G. sanguineum. The detection threshold tested was much lower than that of G. sanguineum HAB, so this technique will be useful for forecasting and preventing G. sanguineum HAB.https://www.academax.com/doi/10.3785/j.issn.1008-9209.2009.02.001<italic>Gymnodinium sanguineum</italic>fluorescent quantitative PCR18S rDNAharmful algal bloom
spellingShingle HE Shan-ying
YU Zhi-gang
A real-time PCR method for rapid detection of Gymnodinium sanguineum
浙江大学学报. 农业与生命科学版
<italic>Gymnodinium sanguineum</italic>
fluorescent quantitative PCR
18S rDNA
harmful algal bloom
title A real-time PCR method for rapid detection of Gymnodinium sanguineum
title_full A real-time PCR method for rapid detection of Gymnodinium sanguineum
title_fullStr A real-time PCR method for rapid detection of Gymnodinium sanguineum
title_full_unstemmed A real-time PCR method for rapid detection of Gymnodinium sanguineum
title_short A real-time PCR method for rapid detection of Gymnodinium sanguineum
title_sort real time pcr method for rapid detection of gymnodinium sanguineum
topic <italic>Gymnodinium sanguineum</italic>
fluorescent quantitative PCR
18S rDNA
harmful algal bloom
url https://www.academax.com/doi/10.3785/j.issn.1008-9209.2009.02.001
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