4.6 Article

Detection of Gambierdiscus and Fukuyoa single cells using recombinase polymerase amplification combined with a sandwich hybridization assay

Journal

JOURNAL OF APPLIED PHYCOLOGY
Volume 33, Issue 4, Pages 2273-2282

Publisher

SPRINGER
DOI: 10.1007/s10811-021-02447-7

Keywords

Gambierdiscus; Fukuyoa; Dinophyceae; Ciguatera; Recombinase polymerase amplification (RPA); Species-specific molecular assay; Single-cell detection

Funding

  1. Ministerio de Ciencia e Innovacion (MICINN)
  2. Agencia Estatal de Investigacion (AEI)
  3. Fondo Europeo de Desarrollo Regional (FEDER) through the CIGUASENSING project [BIO2017-87946-C2-2-R]
  4. European Food Safety Authority through the EuroCigua project [GP/EFSA/AFSCO/2015/03]
  5. CERCA Programme/Generalitat de Catalunya
  6. IRTA-Universitat Rovira i Virgili [2018PMF-PIPF-19]

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The study developed three molecular assays for detecting Gambierdiscus and Fukuyoa genera, as well as G. australes and G. excentricus species, achieving a remarkable limit of detection of a single cell. These assays provide a rapid and cost-effective strategy for reliable screening of samples and ciguatera risk assessment, ensuring seafood safety and protection of human health.
Dinoflagellates of the genera Gambierdiscus and Fukuyoa are known to produce several bioactive compounds including the potent neurotoxic ciguatoxins (CTXs) which are able to accumulate in fish and through the food web. When humans ingest fish contaminated with CTXs, it can result in an intoxication named ciguatera. Although not all the currently recognized species are able to produce toxins, G. australes and G. excentricus have been highlighted to be the most abundant and toxic among the species present in the Atlantic. Even though the genera Gambierdiscus and Fukuyoa are endemic to tropical areas, recently their presence was recorded in subtropical and temperate regions. In this work, the development of three molecular assays for the detection of the Gambierdiscus and Fukuyoa genera and for G. australes and G. excentricus species, based on the combination of recombinase polymerase amplification with detection via hybridization, is successfully described. Furthermore, a remarkable limit of detection of a single cell was achieved. Additionally, six different species have been used to check the ability of each primer set to give an amplified product, even in presence of potentially interfering non-target DNAs. Therefore, these developments provide a rapid and cost-effective strategy for detection of both genera and two of the most toxic species, which will undoubtedly contribute to reliable screening of samples and ciguatera risk assessment, guaranteeing seafood safety and protection of human health.

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