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A novel molecular diagnostic method for the gut content analysis of Philaenus DNA

Philaenus spumarius is a vector of Xylella fastidiosa, one of the most dangerous plants pathogenic bacteria worldwide. There is currently no control measure against this pathogen. Thus, the development of vector control strategies, like generalist predators, such as spiders, could be essential to li...

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Autores principales: Rodrigues, Isabel, Ramos, Vítor, Benhadi-Marín, Jacinto, Moreno, Aránzazu, Fereres, Alberto, Pereira, José Alberto, Baptista, Paula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752687/
https://www.ncbi.nlm.nih.gov/pubmed/35017549
http://dx.doi.org/10.1038/s41598-021-04422-1
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author Rodrigues, Isabel
Ramos, Vítor
Benhadi-Marín, Jacinto
Moreno, Aránzazu
Fereres, Alberto
Pereira, José Alberto
Baptista, Paula
author_facet Rodrigues, Isabel
Ramos, Vítor
Benhadi-Marín, Jacinto
Moreno, Aránzazu
Fereres, Alberto
Pereira, José Alberto
Baptista, Paula
author_sort Rodrigues, Isabel
collection PubMed
description Philaenus spumarius is a vector of Xylella fastidiosa, one of the most dangerous plants pathogenic bacteria worldwide. There is currently no control measure against this pathogen. Thus, the development of vector control strategies, like generalist predators, such as spiders, could be essential to limit the spread of this vector-borne pathogen. In this study, a polymerase chain reaction (PCR)-based approach was developed to principally detect DNA of P. spumarius in the spider’s gut. Accordingly, 20 primer pairs, targeting the mitochondrial cytochrome oxidase I (COI) and cytochrome b (cytB) genes, were tested for specificity, sensitivity, and efficiency in detecting P. spumarius DNA. Overall, two primer sets, targeting COI gene (COI_Ph71F/COI_Ph941R) and the cytB gene (cytB_Ph85F/cytB_Ph635R), showed the highest specificity and sensitivity, being able to amplify 870 pb and 550 bp fragments, respectively, with P. spumarius DNA concentrations 100-fold lower than that of the DNA of non-target species. Among these two primer sets, the cytB_Ph85F/cytB_Ph635R was able to detect P. spumarius in the spider Xysticus acerbus, reaching 50% detection success 82 h after feeding. The feasibility of this primer set to detect predation of P. spumarius by spiders was confirmed in the field, where 20% of the collected spiders presented positive amplifications.
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spelling pubmed-87526872022-01-13 A novel molecular diagnostic method for the gut content analysis of Philaenus DNA Rodrigues, Isabel Ramos, Vítor Benhadi-Marín, Jacinto Moreno, Aránzazu Fereres, Alberto Pereira, José Alberto Baptista, Paula Sci Rep Article Philaenus spumarius is a vector of Xylella fastidiosa, one of the most dangerous plants pathogenic bacteria worldwide. There is currently no control measure against this pathogen. Thus, the development of vector control strategies, like generalist predators, such as spiders, could be essential to limit the spread of this vector-borne pathogen. In this study, a polymerase chain reaction (PCR)-based approach was developed to principally detect DNA of P. spumarius in the spider’s gut. Accordingly, 20 primer pairs, targeting the mitochondrial cytochrome oxidase I (COI) and cytochrome b (cytB) genes, were tested for specificity, sensitivity, and efficiency in detecting P. spumarius DNA. Overall, two primer sets, targeting COI gene (COI_Ph71F/COI_Ph941R) and the cytB gene (cytB_Ph85F/cytB_Ph635R), showed the highest specificity and sensitivity, being able to amplify 870 pb and 550 bp fragments, respectively, with P. spumarius DNA concentrations 100-fold lower than that of the DNA of non-target species. Among these two primer sets, the cytB_Ph85F/cytB_Ph635R was able to detect P. spumarius in the spider Xysticus acerbus, reaching 50% detection success 82 h after feeding. The feasibility of this primer set to detect predation of P. spumarius by spiders was confirmed in the field, where 20% of the collected spiders presented positive amplifications. Nature Publishing Group UK 2022-01-11 /pmc/articles/PMC8752687/ /pubmed/35017549 http://dx.doi.org/10.1038/s41598-021-04422-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Rodrigues, Isabel
Ramos, Vítor
Benhadi-Marín, Jacinto
Moreno, Aránzazu
Fereres, Alberto
Pereira, José Alberto
Baptista, Paula
A novel molecular diagnostic method for the gut content analysis of Philaenus DNA
title A novel molecular diagnostic method for the gut content analysis of Philaenus DNA
title_full A novel molecular diagnostic method for the gut content analysis of Philaenus DNA
title_fullStr A novel molecular diagnostic method for the gut content analysis of Philaenus DNA
title_full_unstemmed A novel molecular diagnostic method for the gut content analysis of Philaenus DNA
title_short A novel molecular diagnostic method for the gut content analysis of Philaenus DNA
title_sort novel molecular diagnostic method for the gut content analysis of philaenus dna
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752687/
https://www.ncbi.nlm.nih.gov/pubmed/35017549
http://dx.doi.org/10.1038/s41598-021-04422-1
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