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A novel duplex qPCR assay for stepwise detection of multiple Perkinsea protistan infections of amphibian tissues

Alveolate protists within the phylum Perkinsea have been found to infect amphibians across a broad taxonomic and geographic range. Phylogenetic analysis has suggested the existence of two clades of amphibian Perkinsea: a putatively non-pathogenic clade linked to asymptomatic infections of tadpoles i...

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Autores principales: Smilansky, Vanessa, Chambouvet, Aurelie, Reeves, Mari, Richards, Thomas A., Milner, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8074936/
https://www.ncbi.nlm.nih.gov/pubmed/33959367
http://dx.doi.org/10.1098/rsos.202150
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author Smilansky, Vanessa
Chambouvet, Aurelie
Reeves, Mari
Richards, Thomas A.
Milner, David S.
author_facet Smilansky, Vanessa
Chambouvet, Aurelie
Reeves, Mari
Richards, Thomas A.
Milner, David S.
author_sort Smilansky, Vanessa
collection PubMed
description Alveolate protists within the phylum Perkinsea have been found to infect amphibians across a broad taxonomic and geographic range. Phylogenetic analysis has suggested the existence of two clades of amphibian Perkinsea: a putatively non-pathogenic clade linked to asymptomatic infections of tadpoles in Africa, Europe and South America, and a putatively pathogenic clade linked to disease and mass mortality events of tadpoles in North America. Here, we describe the development of a duplex TaqMan qPCR assay to detect and discriminate between rDNA sequences from both clades of Perkinsea in amphibian tissues. The assay uses a single primer pair to target an 18S small subunit (SSU) ribosomal RNA (rRNA) gene region shared between the two clades, and two dual-labelled probes to target a region within this fragment that is diagnostic for each clade. This assay enables rapid screening for each of the two Perkinsea groups, allowing for detection, primarily of the phylogenetic group associated with disease outbreaks, and secondarily for the phylogenetic group with no current disease relationship identified. Incorporation of our novel qPCR assay into the routine surveillance of amphibian populations will allow for the assessment of the incidence of each protist clade, thereby providing an improved understanding of Perkinsea infection pervasiveness and a method to underpin future conservation planning.
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spelling pubmed-80749362021-05-05 A novel duplex qPCR assay for stepwise detection of multiple Perkinsea protistan infections of amphibian tissues Smilansky, Vanessa Chambouvet, Aurelie Reeves, Mari Richards, Thomas A. Milner, David S. R Soc Open Sci Biochemistry, Cellular and Molecular Biology Alveolate protists within the phylum Perkinsea have been found to infect amphibians across a broad taxonomic and geographic range. Phylogenetic analysis has suggested the existence of two clades of amphibian Perkinsea: a putatively non-pathogenic clade linked to asymptomatic infections of tadpoles in Africa, Europe and South America, and a putatively pathogenic clade linked to disease and mass mortality events of tadpoles in North America. Here, we describe the development of a duplex TaqMan qPCR assay to detect and discriminate between rDNA sequences from both clades of Perkinsea in amphibian tissues. The assay uses a single primer pair to target an 18S small subunit (SSU) ribosomal RNA (rRNA) gene region shared between the two clades, and two dual-labelled probes to target a region within this fragment that is diagnostic for each clade. This assay enables rapid screening for each of the two Perkinsea groups, allowing for detection, primarily of the phylogenetic group associated with disease outbreaks, and secondarily for the phylogenetic group with no current disease relationship identified. Incorporation of our novel qPCR assay into the routine surveillance of amphibian populations will allow for the assessment of the incidence of each protist clade, thereby providing an improved understanding of Perkinsea infection pervasiveness and a method to underpin future conservation planning. The Royal Society 2021-03-17 /pmc/articles/PMC8074936/ /pubmed/33959367 http://dx.doi.org/10.1098/rsos.202150 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Biochemistry, Cellular and Molecular Biology
Smilansky, Vanessa
Chambouvet, Aurelie
Reeves, Mari
Richards, Thomas A.
Milner, David S.
A novel duplex qPCR assay for stepwise detection of multiple Perkinsea protistan infections of amphibian tissues
title A novel duplex qPCR assay for stepwise detection of multiple Perkinsea protistan infections of amphibian tissues
title_full A novel duplex qPCR assay for stepwise detection of multiple Perkinsea protistan infections of amphibian tissues
title_fullStr A novel duplex qPCR assay for stepwise detection of multiple Perkinsea protistan infections of amphibian tissues
title_full_unstemmed A novel duplex qPCR assay for stepwise detection of multiple Perkinsea protistan infections of amphibian tissues
title_short A novel duplex qPCR assay for stepwise detection of multiple Perkinsea protistan infections of amphibian tissues
title_sort novel duplex qpcr assay for stepwise detection of multiple perkinsea protistan infections of amphibian tissues
topic Biochemistry, Cellular and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8074936/
https://www.ncbi.nlm.nih.gov/pubmed/33959367
http://dx.doi.org/10.1098/rsos.202150
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