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Putative transcription antiterminator RfaH contributes to Erwinia amylovora virulence

The gram‐negative bacterium Erwinia amylovora causes fire blight disease of apple and pear trees. The exopolysaccharide amylovoran and lipopolysaccharides are essential E. amylovora virulence factors. Production of amylovoran and lipopolysaccharide is specified in part by genes that are members of l...

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Autores principales: Klee, Sara M., Sinn, Judith P., Held, Jeremy, Vosburg, Chad, Holmes, Aleah C., Lehman, Brian L., Peter, Kari A., McNellis, Timothy 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/PMC9562583/
https://www.ncbi.nlm.nih.gov/pubmed/35929143
http://dx.doi.org/10.1111/mpp.13254
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author Klee, Sara M.
Sinn, Judith P.
Held, Jeremy
Vosburg, Chad
Holmes, Aleah C.
Lehman, Brian L.
Peter, Kari A.
McNellis, Timothy W.
author_facet Klee, Sara M.
Sinn, Judith P.
Held, Jeremy
Vosburg, Chad
Holmes, Aleah C.
Lehman, Brian L.
Peter, Kari A.
McNellis, Timothy W.
author_sort Klee, Sara M.
collection PubMed
description The gram‐negative bacterium Erwinia amylovora causes fire blight disease of apple and pear trees. The exopolysaccharide amylovoran and lipopolysaccharides are essential E. amylovora virulence factors. Production of amylovoran and lipopolysaccharide is specified in part by genes that are members of long operons. Here, we show that full virulence of E. amylovora in apple fruitlets and tree shoots depends on the predicted transcription antiterminator RfaH. RfaH reduces pausing in the production of long transcripts having an operon polarity suppressor regulatory element within their promoter region. In E. amylovora, only the amylovoran operon and a lipopolysaccharide operon have such regulatory elements within their promoter regions and in the correct orientation. These operons showed dramatically increased polarity in the ΔrfaH mutant compared to the wild type as determined by RNA sequencing. Amylovoran and lipopolysaccharide production in vitro was reduced in rfaH mutants compared to the wild type, which probably contributes to the rfaH mutant virulence phenotype. Furthermore, type VI secretion cluster 1, which contributes to E. amylovora virulence, showed reduced expression in ΔrfaH compared to the wild type, although without an increase in polarity. The data suggest that E. amylovora RfaH directly, specifically, and exclusively suppresses operon polarity in the amylovoran operon and a lipopolysaccharide operon.
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spelling pubmed-95625832022-10-16 Putative transcription antiterminator RfaH contributes to Erwinia amylovora virulence Klee, Sara M. Sinn, Judith P. Held, Jeremy Vosburg, Chad Holmes, Aleah C. Lehman, Brian L. Peter, Kari A. McNellis, Timothy W. Mol Plant Pathol Short Communication The gram‐negative bacterium Erwinia amylovora causes fire blight disease of apple and pear trees. The exopolysaccharide amylovoran and lipopolysaccharides are essential E. amylovora virulence factors. Production of amylovoran and lipopolysaccharide is specified in part by genes that are members of long operons. Here, we show that full virulence of E. amylovora in apple fruitlets and tree shoots depends on the predicted transcription antiterminator RfaH. RfaH reduces pausing in the production of long transcripts having an operon polarity suppressor regulatory element within their promoter region. In E. amylovora, only the amylovoran operon and a lipopolysaccharide operon have such regulatory elements within their promoter regions and in the correct orientation. These operons showed dramatically increased polarity in the ΔrfaH mutant compared to the wild type as determined by RNA sequencing. Amylovoran and lipopolysaccharide production in vitro was reduced in rfaH mutants compared to the wild type, which probably contributes to the rfaH mutant virulence phenotype. Furthermore, type VI secretion cluster 1, which contributes to E. amylovora virulence, showed reduced expression in ΔrfaH compared to the wild type, although without an increase in polarity. The data suggest that E. amylovora RfaH directly, specifically, and exclusively suppresses operon polarity in the amylovoran operon and a lipopolysaccharide operon. John Wiley and Sons Inc. 2022-08-05 /pmc/articles/PMC9562583/ /pubmed/35929143 http://dx.doi.org/10.1111/mpp.13254 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 Short Communication
Klee, Sara M.
Sinn, Judith P.
Held, Jeremy
Vosburg, Chad
Holmes, Aleah C.
Lehman, Brian L.
Peter, Kari A.
McNellis, Timothy W.
Putative transcription antiterminator RfaH contributes to Erwinia amylovora virulence
title Putative transcription antiterminator RfaH contributes to Erwinia amylovora virulence
title_full Putative transcription antiterminator RfaH contributes to Erwinia amylovora virulence
title_fullStr Putative transcription antiterminator RfaH contributes to Erwinia amylovora virulence
title_full_unstemmed Putative transcription antiterminator RfaH contributes to Erwinia amylovora virulence
title_short Putative transcription antiterminator RfaH contributes to Erwinia amylovora virulence
title_sort putative transcription antiterminator rfah contributes to erwinia amylovora virulence
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562583/
https://www.ncbi.nlm.nih.gov/pubmed/35929143
http://dx.doi.org/10.1111/mpp.13254
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