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Metagenomic Sequencing for Identification of Xylella fastidiosa from Leaf Samples

Xylella fastidiosa (Xf) is a globally distributed plant-pathogenic bacterium. The primary control strategy for Xf diseases is eradicating infected plants; therefore, timely and accurate detection is necessary to prevent crop losses and further pathogen dispersal. Conventional Xf diagnostics primaril...

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Autores principales: Román-Reyna, Verónica, Dupas, Enora, Cesbron, Sophie, Marchi, Guido, Campigli, Sara, Hansen, Mary Ann, Bush, Elizabeth, Prarat, Melanie, Shiplett, Katherine, Ivey, Melanie L. Lewis, Pierzynski, Joy, Miller, Sally A., Peduto Hand, Francesca, Jacques, Marie-Agnes, Jacobs, Jonathan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547472/
https://www.ncbi.nlm.nih.gov/pubmed/34698548
http://dx.doi.org/10.1128/mSystems.00591-21
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author Román-Reyna, Verónica
Dupas, Enora
Cesbron, Sophie
Marchi, Guido
Campigli, Sara
Hansen, Mary Ann
Bush, Elizabeth
Prarat, Melanie
Shiplett, Katherine
Ivey, Melanie L. Lewis
Pierzynski, Joy
Miller, Sally A.
Peduto Hand, Francesca
Jacques, Marie-Agnes
Jacobs, Jonathan M.
author_facet Román-Reyna, Verónica
Dupas, Enora
Cesbron, Sophie
Marchi, Guido
Campigli, Sara
Hansen, Mary Ann
Bush, Elizabeth
Prarat, Melanie
Shiplett, Katherine
Ivey, Melanie L. Lewis
Pierzynski, Joy
Miller, Sally A.
Peduto Hand, Francesca
Jacques, Marie-Agnes
Jacobs, Jonathan M.
author_sort Román-Reyna, Verónica
collection PubMed
description Xylella fastidiosa (Xf) is a globally distributed plant-pathogenic bacterium. The primary control strategy for Xf diseases is eradicating infected plants; therefore, timely and accurate detection is necessary to prevent crop losses and further pathogen dispersal. Conventional Xf diagnostics primarily relies on quantitative PCR (qPCR) assays. However, these methods do not consider new or emerging variants due to pathogen genetic recombination and sensitivity limitations. We developed and tested a metagenomics pipeline using in-house short-read sequencing as a complementary approach for affordable, fast, and highly accurate Xf detection. We used metagenomics to identify Xf to the strain level in single- and mixed-infected plant samples at concentrations as low as 1 pg of bacterial DNA per gram of tissue. We also tested naturally infected samples from various plant species originating from Europe and the United States. We identified Xf subspecies in samples previously considered inconclusive with real-time PCR (quantification cycle [C(q)], >35). Overall, we showed the versatility of the pipeline by using different plant hosts and DNA extraction methods. Our pipeline provides taxonomic and functional information for Xf diagnostics without extensive knowledge of the disease. This pipeline demonstrates that metagenomics can be used for early detection of Xf and incorporated as a tool to inform disease management strategies. IMPORTANCE Destructive Xylella fastidiosa (Xf) outbreaks in Europe highlight this pathogen’s capacity to expand its host range and geographical distribution. The current disease diagnostic approaches are limited by a multiple-step process, biases to known sequences, and detection limits. We developed a low-cost, user-friendly metagenomic sequencing tool for Xf detection. In less than 3 days, we were able to identify Xf subspecies and strains in field-collected samples. Overall, our pipeline is a diagnostics tool that could be easily extended to other plant-pathogen interactions and implemented for emerging plant threat surveillance.
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spelling pubmed-85474722021-10-27 Metagenomic Sequencing for Identification of Xylella fastidiosa from Leaf Samples Román-Reyna, Verónica Dupas, Enora Cesbron, Sophie Marchi, Guido Campigli, Sara Hansen, Mary Ann Bush, Elizabeth Prarat, Melanie Shiplett, Katherine Ivey, Melanie L. Lewis Pierzynski, Joy Miller, Sally A. Peduto Hand, Francesca Jacques, Marie-Agnes Jacobs, Jonathan M. mSystems Methods and Protocols Xylella fastidiosa (Xf) is a globally distributed plant-pathogenic bacterium. The primary control strategy for Xf diseases is eradicating infected plants; therefore, timely and accurate detection is necessary to prevent crop losses and further pathogen dispersal. Conventional Xf diagnostics primarily relies on quantitative PCR (qPCR) assays. However, these methods do not consider new or emerging variants due to pathogen genetic recombination and sensitivity limitations. We developed and tested a metagenomics pipeline using in-house short-read sequencing as a complementary approach for affordable, fast, and highly accurate Xf detection. We used metagenomics to identify Xf to the strain level in single- and mixed-infected plant samples at concentrations as low as 1 pg of bacterial DNA per gram of tissue. We also tested naturally infected samples from various plant species originating from Europe and the United States. We identified Xf subspecies in samples previously considered inconclusive with real-time PCR (quantification cycle [C(q)], >35). Overall, we showed the versatility of the pipeline by using different plant hosts and DNA extraction methods. Our pipeline provides taxonomic and functional information for Xf diagnostics without extensive knowledge of the disease. This pipeline demonstrates that metagenomics can be used for early detection of Xf and incorporated as a tool to inform disease management strategies. IMPORTANCE Destructive Xylella fastidiosa (Xf) outbreaks in Europe highlight this pathogen’s capacity to expand its host range and geographical distribution. The current disease diagnostic approaches are limited by a multiple-step process, biases to known sequences, and detection limits. We developed a low-cost, user-friendly metagenomic sequencing tool for Xf detection. In less than 3 days, we were able to identify Xf subspecies and strains in field-collected samples. Overall, our pipeline is a diagnostics tool that could be easily extended to other plant-pathogen interactions and implemented for emerging plant threat surveillance. American Society for Microbiology 2021-10-26 /pmc/articles/PMC8547472/ /pubmed/34698548 http://dx.doi.org/10.1128/mSystems.00591-21 Text en Copyright © 2021 Román-Reyna et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Methods and Protocols
Román-Reyna, Verónica
Dupas, Enora
Cesbron, Sophie
Marchi, Guido
Campigli, Sara
Hansen, Mary Ann
Bush, Elizabeth
Prarat, Melanie
Shiplett, Katherine
Ivey, Melanie L. Lewis
Pierzynski, Joy
Miller, Sally A.
Peduto Hand, Francesca
Jacques, Marie-Agnes
Jacobs, Jonathan M.
Metagenomic Sequencing for Identification of Xylella fastidiosa from Leaf Samples
title Metagenomic Sequencing for Identification of Xylella fastidiosa from Leaf Samples
title_full Metagenomic Sequencing for Identification of Xylella fastidiosa from Leaf Samples
title_fullStr Metagenomic Sequencing for Identification of Xylella fastidiosa from Leaf Samples
title_full_unstemmed Metagenomic Sequencing for Identification of Xylella fastidiosa from Leaf Samples
title_short Metagenomic Sequencing for Identification of Xylella fastidiosa from Leaf Samples
title_sort metagenomic sequencing for identification of xylella fastidiosa from leaf samples
topic Methods and Protocols
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547472/
https://www.ncbi.nlm.nih.gov/pubmed/34698548
http://dx.doi.org/10.1128/mSystems.00591-21
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