New real-time PCR assay for toxigenic Amphidoma languida

Azaspiracids (AZA) are a group of lipophilic toxins, which are produced by a few species of the marine nanoplanktonic dinoflagellate genera Azadinium and Amphidoma (Amphidomataceae). Amphidomataceae were found to be globally distributed in coastal waters and new areas of occurrence are regularly dis...

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Main Authors: Wietkamp, Stephan, Tillmann, Urban, Clarke, Dave, Toebe, Kerstin
Format: Conference Object
Language:unknown
Published: 2018
Subjects:
Online Access:https://epic.awi.de/id/eprint/48263/
https://epic.awi.de/id/eprint/48263/1/ICHA_2018_Poster_SWietkamp.pdf
https://hdl.handle.net/10013/epic.4e76f99e-b6a0-4d74-add2-6ebf4ee18be4
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spelling ftawi:oai:epic.awi.de:48263 2024-09-15T18:14:23+00:00 New real-time PCR assay for toxigenic Amphidoma languida Wietkamp, Stephan Tillmann, Urban Clarke, Dave Toebe, Kerstin 2018-10-22 application/pdf https://epic.awi.de/id/eprint/48263/ https://epic.awi.de/id/eprint/48263/1/ICHA_2018_Poster_SWietkamp.pdf https://hdl.handle.net/10013/epic.4e76f99e-b6a0-4d74-add2-6ebf4ee18be4 unknown https://epic.awi.de/id/eprint/48263/1/ICHA_2018_Poster_SWietkamp.pdf Wietkamp, S. orcid:0000-0001-7516-9861 , Tillmann, U. orcid:0000-0002-8207-4382 , Clarke, D. and Toebe, K. (2018) New real-time PCR assay for toxigenic Amphidoma languida , ICHA 2018 - International Conference on Harmful Algae, Nantes, France, 21 October 2018 - 26 October 2018 . hdl:10013/epic.4e76f99e-b6a0-4d74-add2-6ebf4ee18be4 EPIC3ICHA 2018 - International Conference on Harmful Algae, Nantes, France, 2018-10-21-2018-10-26 Conference notRev 2018 ftawi 2024-06-24T04:21:00Z Azaspiracids (AZA) are a group of lipophilic toxins, which are produced by a few species of the marine nanoplanktonic dinoflagellate genera Azadinium and Amphidoma (Amphidomataceae). Amphidomataceae were found to be globally distributed in coastal waters and new areas of occurrence are regularly discovered. The AZA toxins accumulate mainly in shellfish and - when consumed by humans - can lead to the so-called azaspiracid shellfish poisoning syndrome (AZP). Given this serious threat to seafood production and to deepen knowledge about the distribution and risk potential of AZA-producing algae, an appropriate detection method enabling a fast identification and quantification for these toxigenic species is needed. Traditional light microscopy is time-consuming, requires expertise and is getting rather difficult when it comes to the detection, identification and quantification of small-sized plankton. To overcome this challenges, quantitative real-time PCR (qPCR) assays are increasingly used as a molecular additive. Basically, when amplifying the extracted DNA and using DNA standards, the amplification threshold (CT) gives information about the number of target species in the sample. For two AZA-producing species, Azadinium spinosum and Azadinium poporum, quantitative PCR assays have already been developed and successfully applied in the field. Another AZA-producing species, Amphidoma languida, was discovered in 2012 in Irish coastal waters and discovered as a new species within the group of Amphidomataceae - in close relationship with Azadinium spp. All available strains from Ireland, Iceland, Norway, Denmark and Spain produce azaspiracids. Moreover, Am. languida from the Atlantic coast of southern Spain was responsible for AZA amounts in shellfish above the EU regulatory limit, emphasizing the need for further investigations. We thus developed a quantitative TaqMan PCR assay, amplifying 60bp of the D2 region (located on the LSU/28S) of the ribosomal DNA (rDNA) to detect toxic Am. languida. To confirm assay ... Conference Object Iceland Alfred Wegener Institute for Polar- and Marine Research (AWI): ePIC (electronic Publication Information Center)
institution Open Polar
collection Alfred Wegener Institute for Polar- and Marine Research (AWI): ePIC (electronic Publication Information Center)
op_collection_id ftawi
language unknown
description Azaspiracids (AZA) are a group of lipophilic toxins, which are produced by a few species of the marine nanoplanktonic dinoflagellate genera Azadinium and Amphidoma (Amphidomataceae). Amphidomataceae were found to be globally distributed in coastal waters and new areas of occurrence are regularly discovered. The AZA toxins accumulate mainly in shellfish and - when consumed by humans - can lead to the so-called azaspiracid shellfish poisoning syndrome (AZP). Given this serious threat to seafood production and to deepen knowledge about the distribution and risk potential of AZA-producing algae, an appropriate detection method enabling a fast identification and quantification for these toxigenic species is needed. Traditional light microscopy is time-consuming, requires expertise and is getting rather difficult when it comes to the detection, identification and quantification of small-sized plankton. To overcome this challenges, quantitative real-time PCR (qPCR) assays are increasingly used as a molecular additive. Basically, when amplifying the extracted DNA and using DNA standards, the amplification threshold (CT) gives information about the number of target species in the sample. For two AZA-producing species, Azadinium spinosum and Azadinium poporum, quantitative PCR assays have already been developed and successfully applied in the field. Another AZA-producing species, Amphidoma languida, was discovered in 2012 in Irish coastal waters and discovered as a new species within the group of Amphidomataceae - in close relationship with Azadinium spp. All available strains from Ireland, Iceland, Norway, Denmark and Spain produce azaspiracids. Moreover, Am. languida from the Atlantic coast of southern Spain was responsible for AZA amounts in shellfish above the EU regulatory limit, emphasizing the need for further investigations. We thus developed a quantitative TaqMan PCR assay, amplifying 60bp of the D2 region (located on the LSU/28S) of the ribosomal DNA (rDNA) to detect toxic Am. languida. To confirm assay ...
format Conference Object
author Wietkamp, Stephan
Tillmann, Urban
Clarke, Dave
Toebe, Kerstin
spellingShingle Wietkamp, Stephan
Tillmann, Urban
Clarke, Dave
Toebe, Kerstin
New real-time PCR assay for toxigenic Amphidoma languida
author_facet Wietkamp, Stephan
Tillmann, Urban
Clarke, Dave
Toebe, Kerstin
author_sort Wietkamp, Stephan
title New real-time PCR assay for toxigenic Amphidoma languida
title_short New real-time PCR assay for toxigenic Amphidoma languida
title_full New real-time PCR assay for toxigenic Amphidoma languida
title_fullStr New real-time PCR assay for toxigenic Amphidoma languida
title_full_unstemmed New real-time PCR assay for toxigenic Amphidoma languida
title_sort new real-time pcr assay for toxigenic amphidoma languida
publishDate 2018
url https://epic.awi.de/id/eprint/48263/
https://epic.awi.de/id/eprint/48263/1/ICHA_2018_Poster_SWietkamp.pdf
https://hdl.handle.net/10013/epic.4e76f99e-b6a0-4d74-add2-6ebf4ee18be4
genre Iceland
genre_facet Iceland
op_source EPIC3ICHA 2018 - International Conference on Harmful Algae, Nantes, France, 2018-10-21-2018-10-26
op_relation https://epic.awi.de/id/eprint/48263/1/ICHA_2018_Poster_SWietkamp.pdf
Wietkamp, S. orcid:0000-0001-7516-9861 , Tillmann, U. orcid:0000-0002-8207-4382 , Clarke, D. and Toebe, K. (2018) New real-time PCR assay for toxigenic Amphidoma languida , ICHA 2018 - International Conference on Harmful Algae, Nantes, France, 21 October 2018 - 26 October 2018 . hdl:10013/epic.4e76f99e-b6a0-4d74-add2-6ebf4ee18be4
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