Cargando…
The stringent response regulator (p) ppGpp mediates virulence gene expression and survival in Erwinia amylovora
BACKGROUND: The nucleotide second messengers, i.e., guanosine tetraphosphate and pentaphosphate [collectively referred to as (p) ppGpp], trigger the stringent response under nutrient starvation conditions and play an essential role in virulence in the fire blight pathogen Erwinia amylovora. Here, we...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106674/ https://www.ncbi.nlm.nih.gov/pubmed/32228459 http://dx.doi.org/10.1186/s12864-020-6699-5 |
_version_ | 1783512658798968832 |
---|---|
author | Yang, Ho-wen Yu, Menghao Lee, Jae Hoon Chatnaparat, Tiyakhon Zhao, Youfu |
author_facet | Yang, Ho-wen Yu, Menghao Lee, Jae Hoon Chatnaparat, Tiyakhon Zhao, Youfu |
author_sort | Yang, Ho-wen |
collection | PubMed |
description | BACKGROUND: The nucleotide second messengers, i.e., guanosine tetraphosphate and pentaphosphate [collectively referred to as (p) ppGpp], trigger the stringent response under nutrient starvation conditions and play an essential role in virulence in the fire blight pathogen Erwinia amylovora. Here, we present transcriptomic analyses to uncover the overall effect of (p) ppGpp-mediated stringent response in E. amylovora in the hrp-inducing minimal medium (HMM). RESULTS: In this study, we investigated the transcriptomic changes of the (p) ppGpp(0) mutant under the type III secretion system (T3SS)-inducing condition using RNA-seq. A total of 1314 differentially expressed genes (DEGs) was uncovered, representing more than one third (36.8%) of all genes in the E. amylovora genome. Compared to the wild-type, the (p) ppGpp(0) mutant showed down-regulation of genes involved in peptide ATP-binding cassette (ABC) transporters and virulence-related processes, including type III secretion system (T3SS), biofilm, and motility. Interestingly, in contrast to previous reports, the (p) ppGpp(0) mutant showed up-regulation of amino acid biosynthesis genes, suggesting that it might be due to that these amino acid biosynthesis genes are indirectly regulated by (p) ppGpp in E. amylovora or represent specific culturing condition used. Furthermore, the (p) ppGpp(0) mutant exhibited up-regulation of genes involved in translation, SOS response, DNA replication, chromosome segregation, as well as biosynthesis of nucleotide, fatty acid and lipid. CONCLUSION: These findings suggested that in HMM environment, E. amylovora might use (p) ppGpp as a signal to activate virulence gene expression, and simultaneously mediate the balance between virulence and survival by negatively regulating DNA replication, translation, cell division, as well as biosynthesis of nucleotide, amino acid, fatty acid, and lipid. Therefore, (p) ppGpp could be a promising target for developing novel control measures to fight against this devastating disease of apples and pears. |
format | Online Article Text |
id | pubmed-7106674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71066742020-04-01 The stringent response regulator (p) ppGpp mediates virulence gene expression and survival in Erwinia amylovora Yang, Ho-wen Yu, Menghao Lee, Jae Hoon Chatnaparat, Tiyakhon Zhao, Youfu BMC Genomics Research Article BACKGROUND: The nucleotide second messengers, i.e., guanosine tetraphosphate and pentaphosphate [collectively referred to as (p) ppGpp], trigger the stringent response under nutrient starvation conditions and play an essential role in virulence in the fire blight pathogen Erwinia amylovora. Here, we present transcriptomic analyses to uncover the overall effect of (p) ppGpp-mediated stringent response in E. amylovora in the hrp-inducing minimal medium (HMM). RESULTS: In this study, we investigated the transcriptomic changes of the (p) ppGpp(0) mutant under the type III secretion system (T3SS)-inducing condition using RNA-seq. A total of 1314 differentially expressed genes (DEGs) was uncovered, representing more than one third (36.8%) of all genes in the E. amylovora genome. Compared to the wild-type, the (p) ppGpp(0) mutant showed down-regulation of genes involved in peptide ATP-binding cassette (ABC) transporters and virulence-related processes, including type III secretion system (T3SS), biofilm, and motility. Interestingly, in contrast to previous reports, the (p) ppGpp(0) mutant showed up-regulation of amino acid biosynthesis genes, suggesting that it might be due to that these amino acid biosynthesis genes are indirectly regulated by (p) ppGpp in E. amylovora or represent specific culturing condition used. Furthermore, the (p) ppGpp(0) mutant exhibited up-regulation of genes involved in translation, SOS response, DNA replication, chromosome segregation, as well as biosynthesis of nucleotide, fatty acid and lipid. CONCLUSION: These findings suggested that in HMM environment, E. amylovora might use (p) ppGpp as a signal to activate virulence gene expression, and simultaneously mediate the balance between virulence and survival by negatively regulating DNA replication, translation, cell division, as well as biosynthesis of nucleotide, amino acid, fatty acid, and lipid. Therefore, (p) ppGpp could be a promising target for developing novel control measures to fight against this devastating disease of apples and pears. BioMed Central 2020-03-30 /pmc/articles/PMC7106674/ /pubmed/32228459 http://dx.doi.org/10.1186/s12864-020-6699-5 Text en © The Author(s). 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Yang, Ho-wen Yu, Menghao Lee, Jae Hoon Chatnaparat, Tiyakhon Zhao, Youfu The stringent response regulator (p) ppGpp mediates virulence gene expression and survival in Erwinia amylovora |
title | The stringent response regulator (p) ppGpp mediates virulence gene expression and survival in Erwinia amylovora |
title_full | The stringent response regulator (p) ppGpp mediates virulence gene expression and survival in Erwinia amylovora |
title_fullStr | The stringent response regulator (p) ppGpp mediates virulence gene expression and survival in Erwinia amylovora |
title_full_unstemmed | The stringent response regulator (p) ppGpp mediates virulence gene expression and survival in Erwinia amylovora |
title_short | The stringent response regulator (p) ppGpp mediates virulence gene expression and survival in Erwinia amylovora |
title_sort | stringent response regulator (p) ppgpp mediates virulence gene expression and survival in erwinia amylovora |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106674/ https://www.ncbi.nlm.nih.gov/pubmed/32228459 http://dx.doi.org/10.1186/s12864-020-6699-5 |
work_keys_str_mv | AT yanghowen thestringentresponseregulatorpppgppmediatesvirulencegeneexpressionandsurvivalinerwiniaamylovora AT yumenghao thestringentresponseregulatorpppgppmediatesvirulencegeneexpressionandsurvivalinerwiniaamylovora AT leejaehoon thestringentresponseregulatorpppgppmediatesvirulencegeneexpressionandsurvivalinerwiniaamylovora AT chatnaparattiyakhon thestringentresponseregulatorpppgppmediatesvirulencegeneexpressionandsurvivalinerwiniaamylovora AT zhaoyoufu thestringentresponseregulatorpppgppmediatesvirulencegeneexpressionandsurvivalinerwiniaamylovora AT yanghowen stringentresponseregulatorpppgppmediatesvirulencegeneexpressionandsurvivalinerwiniaamylovora AT yumenghao stringentresponseregulatorpppgppmediatesvirulencegeneexpressionandsurvivalinerwiniaamylovora AT leejaehoon stringentresponseregulatorpppgppmediatesvirulencegeneexpressionandsurvivalinerwiniaamylovora AT chatnaparattiyakhon stringentresponseregulatorpppgppmediatesvirulencegeneexpressionandsurvivalinerwiniaamylovora AT zhaoyoufu stringentresponseregulatorpppgppmediatesvirulencegeneexpressionandsurvivalinerwiniaamylovora |