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Genomic and functional analysis of phage‐mediated horizontal gene transfer in Pseudomonas syringae on the plant surface

Many strains of Pseudomonas colonise plant surfaces, including the cherry canker pathogens, Pseudomonas syringae pathovars syringae and morsprunorum. We have examined the genomic diversity of P. syringae in the cherry phyllosphere and focused on the role of prophages in transfer of genes encoding Ty...

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Autores principales: Hulin, Michelle T., Rabiey, Mojgan, Zeng, Ziyue, Vadillo Dieguez, Andrea, Bellamy, Sophia, Swift, Phoebe, Mansfield, John W., Jackson, Robert W., Harrison, Richard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107160/
https://www.ncbi.nlm.nih.gov/pubmed/36285389
http://dx.doi.org/10.1111/nph.18573
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author Hulin, Michelle T.
Rabiey, Mojgan
Zeng, Ziyue
Vadillo Dieguez, Andrea
Bellamy, Sophia
Swift, Phoebe
Mansfield, John W.
Jackson, Robert W.
Harrison, Richard J.
author_facet Hulin, Michelle T.
Rabiey, Mojgan
Zeng, Ziyue
Vadillo Dieguez, Andrea
Bellamy, Sophia
Swift, Phoebe
Mansfield, John W.
Jackson, Robert W.
Harrison, Richard J.
author_sort Hulin, Michelle T.
collection PubMed
description Many strains of Pseudomonas colonise plant surfaces, including the cherry canker pathogens, Pseudomonas syringae pathovars syringae and morsprunorum. We have examined the genomic diversity of P. syringae in the cherry phyllosphere and focused on the role of prophages in transfer of genes encoding Type 3 secreted effector (T3SE) proteins contributing to the evolution of virulence. Phylogenomic analysis was carried out on epiphytic pseudomonads in the UK orchards. Significant differences in epiphytic populations occurred between regions. Nonpathogenic strains were found to contain reservoirs of T3SE genes. Members of P. syringae phylogroups 4 and 10 were identified for the first time from Prunus. Using bioinformatics, we explored the presence of the gene encoding T3SE HopAR1 within related prophage sequences in diverse P. syringae strains including cherry epiphytes and pathogens. Results indicated that horizontal gene transfer (HGT) of this effector between phylogroups may have involved phage. Prophages containing hopAR1 were demonstrated to excise, circularise and transfer the gene on the leaf surface. The phyllosphere provides a dynamic environment for prophage‐mediated gene exchange and the potential for the emergence of new more virulent pathotypes. Our results suggest that genome‐based epidemiological surveillance of environmental populations will allow the timely application of control measures to prevent damaging diseases.
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spelling pubmed-101071602023-04-18 Genomic and functional analysis of phage‐mediated horizontal gene transfer in Pseudomonas syringae on the plant surface Hulin, Michelle T. Rabiey, Mojgan Zeng, Ziyue Vadillo Dieguez, Andrea Bellamy, Sophia Swift, Phoebe Mansfield, John W. Jackson, Robert W. Harrison, Richard J. New Phytol Research Many strains of Pseudomonas colonise plant surfaces, including the cherry canker pathogens, Pseudomonas syringae pathovars syringae and morsprunorum. We have examined the genomic diversity of P. syringae in the cherry phyllosphere and focused on the role of prophages in transfer of genes encoding Type 3 secreted effector (T3SE) proteins contributing to the evolution of virulence. Phylogenomic analysis was carried out on epiphytic pseudomonads in the UK orchards. Significant differences in epiphytic populations occurred between regions. Nonpathogenic strains were found to contain reservoirs of T3SE genes. Members of P. syringae phylogroups 4 and 10 were identified for the first time from Prunus. Using bioinformatics, we explored the presence of the gene encoding T3SE HopAR1 within related prophage sequences in diverse P. syringae strains including cherry epiphytes and pathogens. Results indicated that horizontal gene transfer (HGT) of this effector between phylogroups may have involved phage. Prophages containing hopAR1 were demonstrated to excise, circularise and transfer the gene on the leaf surface. The phyllosphere provides a dynamic environment for prophage‐mediated gene exchange and the potential for the emergence of new more virulent pathotypes. Our results suggest that genome‐based epidemiological surveillance of environmental populations will allow the timely application of control measures to prevent damaging diseases. John Wiley and Sons Inc. 2022-12-02 2023-02 /pmc/articles/PMC10107160/ /pubmed/36285389 http://dx.doi.org/10.1111/nph.18573 Text en © 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Hulin, Michelle T.
Rabiey, Mojgan
Zeng, Ziyue
Vadillo Dieguez, Andrea
Bellamy, Sophia
Swift, Phoebe
Mansfield, John W.
Jackson, Robert W.
Harrison, Richard J.
Genomic and functional analysis of phage‐mediated horizontal gene transfer in Pseudomonas syringae on the plant surface
title Genomic and functional analysis of phage‐mediated horizontal gene transfer in Pseudomonas syringae on the plant surface
title_full Genomic and functional analysis of phage‐mediated horizontal gene transfer in Pseudomonas syringae on the plant surface
title_fullStr Genomic and functional analysis of phage‐mediated horizontal gene transfer in Pseudomonas syringae on the plant surface
title_full_unstemmed Genomic and functional analysis of phage‐mediated horizontal gene transfer in Pseudomonas syringae on the plant surface
title_short Genomic and functional analysis of phage‐mediated horizontal gene transfer in Pseudomonas syringae on the plant surface
title_sort genomic and functional analysis of phage‐mediated horizontal gene transfer in pseudomonas syringae on the plant surface
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107160/
https://www.ncbi.nlm.nih.gov/pubmed/36285389
http://dx.doi.org/10.1111/nph.18573
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