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Identification of novel virulence factors in Erwinia amylovora through temporal transcriptomic analysis of infected apple flowers under field conditions

The enterobacterial pathogen Erwinia amylovora uses multiple virulence‐associated traits to cause fire blight, a devastating disease of apple and pear trees. Many virulence‐associated phenotypes have been studied that are critical for virulence and pathogenicity. Despite the in vitro testing that ha...

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Autores principales: Schachterle, Jeffrey K., Gdanetz, Kristi, Pandya, Ishani, Sundin, George W.
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/PMC9104256/
https://www.ncbi.nlm.nih.gov/pubmed/35246928
http://dx.doi.org/10.1111/mpp.13199
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author Schachterle, Jeffrey K.
Gdanetz, Kristi
Pandya, Ishani
Sundin, George W.
author_facet Schachterle, Jeffrey K.
Gdanetz, Kristi
Pandya, Ishani
Sundin, George W.
author_sort Schachterle, Jeffrey K.
collection PubMed
description The enterobacterial pathogen Erwinia amylovora uses multiple virulence‐associated traits to cause fire blight, a devastating disease of apple and pear trees. Many virulence‐associated phenotypes have been studied that are critical for virulence and pathogenicity. Despite the in vitro testing that has revealed how these systems are transcriptionally regulated, information on when and where in infected tissues these genes are being expressed is lacking. Here, we used a high‐throughput sequencing approach to characterize the transcriptome of E. amylovora during disease progression on apple flowers under field infection conditions. We report that type III secretion system genes and flagellar genes are strongly co‐expressed. Likewise, genes involved in biosynthesis of the exopolysaccharide amylovoran and sorbitol utilization had similar expression patterns. We further identified a group of 16 genes whose expression is increased and maintained at high levels throughout disease progression across time and tissues. We chose five of these genes for mutational analysis and observed that deletion mutants lacking these genes all display reduced symptom development on apple shoots. Furthermore, these induced genes were over‐represented for genes involved in sulphur metabolism and cycling, suggesting the possibility of an important role for maintenance of oxidative homeostasis during apple flower infection.
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spelling pubmed-91042562022-05-18 Identification of novel virulence factors in Erwinia amylovora through temporal transcriptomic analysis of infected apple flowers under field conditions Schachterle, Jeffrey K. Gdanetz, Kristi Pandya, Ishani Sundin, George W. Mol Plant Pathol Original Articles The enterobacterial pathogen Erwinia amylovora uses multiple virulence‐associated traits to cause fire blight, a devastating disease of apple and pear trees. Many virulence‐associated phenotypes have been studied that are critical for virulence and pathogenicity. Despite the in vitro testing that has revealed how these systems are transcriptionally regulated, information on when and where in infected tissues these genes are being expressed is lacking. Here, we used a high‐throughput sequencing approach to characterize the transcriptome of E. amylovora during disease progression on apple flowers under field infection conditions. We report that type III secretion system genes and flagellar genes are strongly co‐expressed. Likewise, genes involved in biosynthesis of the exopolysaccharide amylovoran and sorbitol utilization had similar expression patterns. We further identified a group of 16 genes whose expression is increased and maintained at high levels throughout disease progression across time and tissues. We chose five of these genes for mutational analysis and observed that deletion mutants lacking these genes all display reduced symptom development on apple shoots. Furthermore, these induced genes were over‐represented for genes involved in sulphur metabolism and cycling, suggesting the possibility of an important role for maintenance of oxidative homeostasis during apple flower infection. John Wiley and Sons Inc. 2022-03-04 /pmc/articles/PMC9104256/ /pubmed/35246928 http://dx.doi.org/10.1111/mpp.13199 Text en © 2022 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Schachterle, Jeffrey K.
Gdanetz, Kristi
Pandya, Ishani
Sundin, George W.
Identification of novel virulence factors in Erwinia amylovora through temporal transcriptomic analysis of infected apple flowers under field conditions
title Identification of novel virulence factors in Erwinia amylovora through temporal transcriptomic analysis of infected apple flowers under field conditions
title_full Identification of novel virulence factors in Erwinia amylovora through temporal transcriptomic analysis of infected apple flowers under field conditions
title_fullStr Identification of novel virulence factors in Erwinia amylovora through temporal transcriptomic analysis of infected apple flowers under field conditions
title_full_unstemmed Identification of novel virulence factors in Erwinia amylovora through temporal transcriptomic analysis of infected apple flowers under field conditions
title_short Identification of novel virulence factors in Erwinia amylovora through temporal transcriptomic analysis of infected apple flowers under field conditions
title_sort identification of novel virulence factors in erwinia amylovora through temporal transcriptomic analysis of infected apple flowers under field conditions
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104256/
https://www.ncbi.nlm.nih.gov/pubmed/35246928
http://dx.doi.org/10.1111/mpp.13199
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