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CsrD regulates amylovoran biosynthesis and virulence in Erwinia amylovora in a novel cyclic‐di‐GMP dependent manner

Erwinia amylovora is an economically devastating plant pathogen that causes fire blight disease in members of the Rosaceae family, most notably in apple and pear. The exopolysaccharide amylovoran is a pathogenicity determinant in E. amylovora and a major component of the extracellular matrix of biof...

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Autores principales: Kharadi, Roshni R., 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/PMC9276943/
https://www.ncbi.nlm.nih.gov/pubmed/35396793
http://dx.doi.org/10.1111/mpp.13217
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author Kharadi, Roshni R.
Sundin, George W.
author_facet Kharadi, Roshni R.
Sundin, George W.
author_sort Kharadi, Roshni R.
collection PubMed
description Erwinia amylovora is an economically devastating plant pathogen that causes fire blight disease in members of the Rosaceae family, most notably in apple and pear. The exopolysaccharide amylovoran is a pathogenicity determinant in E. amylovora and a major component of the extracellular matrix of biofilms formed within the xylem vasculature of the host plant. The second messenger cyclic‐di‐GMP (c‐di‐GMP) has been reported to positively regulate the transcription of amsG (the first gene in the 12‐gene amylovoran [ams] biosynthetic operon), thus impacting amylovoran production. However, the regulatory mechanism by which this interaction occurs is largely unknown. Here, we report that c‐di‐GMP can bind to specific residues in the EAL domain of the E. amylovora protein CsrD. CsrD and RNase E regulate the degradation of the sRNA CsrB in E. amylovora. When CsrD is bound to c‐di‐GMP, there is an enhancement in the level of RNase E‐mediated degradation of CsrB, which then alters amsG transcription. Additionally, csrD was also found to positively contribute to virulence and biofilm formation. We thus present a pathway of conditional regulation of amylovoran production mediated by changing intracellular levels of c‐di‐GMP, which impacts disease progression.
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spelling pubmed-92769432022-07-15 CsrD regulates amylovoran biosynthesis and virulence in Erwinia amylovora in a novel cyclic‐di‐GMP dependent manner Kharadi, Roshni R. Sundin, George W. Mol Plant Pathol Original Articles Erwinia amylovora is an economically devastating plant pathogen that causes fire blight disease in members of the Rosaceae family, most notably in apple and pear. The exopolysaccharide amylovoran is a pathogenicity determinant in E. amylovora and a major component of the extracellular matrix of biofilms formed within the xylem vasculature of the host plant. The second messenger cyclic‐di‐GMP (c‐di‐GMP) has been reported to positively regulate the transcription of amsG (the first gene in the 12‐gene amylovoran [ams] biosynthetic operon), thus impacting amylovoran production. However, the regulatory mechanism by which this interaction occurs is largely unknown. Here, we report that c‐di‐GMP can bind to specific residues in the EAL domain of the E. amylovora protein CsrD. CsrD and RNase E regulate the degradation of the sRNA CsrB in E. amylovora. When CsrD is bound to c‐di‐GMP, there is an enhancement in the level of RNase E‐mediated degradation of CsrB, which then alters amsG transcription. Additionally, csrD was also found to positively contribute to virulence and biofilm formation. We thus present a pathway of conditional regulation of amylovoran production mediated by changing intracellular levels of c‐di‐GMP, which impacts disease progression. John Wiley and Sons Inc. 2022-04-09 /pmc/articles/PMC9276943/ /pubmed/35396793 http://dx.doi.org/10.1111/mpp.13217 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
Kharadi, Roshni R.
Sundin, George W.
CsrD regulates amylovoran biosynthesis and virulence in Erwinia amylovora in a novel cyclic‐di‐GMP dependent manner
title CsrD regulates amylovoran biosynthesis and virulence in Erwinia amylovora in a novel cyclic‐di‐GMP dependent manner
title_full CsrD regulates amylovoran biosynthesis and virulence in Erwinia amylovora in a novel cyclic‐di‐GMP dependent manner
title_fullStr CsrD regulates amylovoran biosynthesis and virulence in Erwinia amylovora in a novel cyclic‐di‐GMP dependent manner
title_full_unstemmed CsrD regulates amylovoran biosynthesis and virulence in Erwinia amylovora in a novel cyclic‐di‐GMP dependent manner
title_short CsrD regulates amylovoran biosynthesis and virulence in Erwinia amylovora in a novel cyclic‐di‐GMP dependent manner
title_sort csrd regulates amylovoran biosynthesis and virulence in erwinia amylovora in a novel cyclic‐di‐gmp dependent manner
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276943/
https://www.ncbi.nlm.nih.gov/pubmed/35396793
http://dx.doi.org/10.1111/mpp.13217
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AT sundingeorgew csrdregulatesamylovoranbiosynthesisandvirulenceinerwiniaamylovorainanovelcyclicdigmpdependentmanner