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Plant-Pathogenic Ralstonia Phylotypes Evolved Divergent Respiratory Strategies and Behaviors To Thrive in Xylem
Bacterial pathogens in the Ralstonia solanacearum species complex (RSSC) infect the water-transporting xylem vessels of plants, causing bacterial wilt disease. Strains in RSSC phylotypes I and III can reduce nitrate to dinitrogen via complete denitrification. The four-step denitrification pathway en...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9973335/ https://www.ncbi.nlm.nih.gov/pubmed/36744950 http://dx.doi.org/10.1128/mbio.03188-22 |
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author | Truchon, Alicia N. Dalsing, Beth L. Khokhani, Devanshi MacIntyre, April McDonald, Bradon R. Ailloud, Florent Klassen, Jonathan Gonzalez-Orta, Enid T. Currie, Cameron Prior, Philippe Lowe-Power, Tiffany M. Allen, Caitilyn |
author_facet | Truchon, Alicia N. Dalsing, Beth L. Khokhani, Devanshi MacIntyre, April McDonald, Bradon R. Ailloud, Florent Klassen, Jonathan Gonzalez-Orta, Enid T. Currie, Cameron Prior, Philippe Lowe-Power, Tiffany M. Allen, Caitilyn |
author_sort | Truchon, Alicia N. |
collection | PubMed |
description | Bacterial pathogens in the Ralstonia solanacearum species complex (RSSC) infect the water-transporting xylem vessels of plants, causing bacterial wilt disease. Strains in RSSC phylotypes I and III can reduce nitrate to dinitrogen via complete denitrification. The four-step denitrification pathway enables bacteria to use inorganic nitrogen species as terminal electron acceptors, supporting their growth in oxygen-limited environments such as biofilms or plant xylem. Reduction of nitrate, nitrite, and nitric oxide all contribute to the virulence of a model phylotype I strain. However, little is known about the physiological role of the last denitrification step, the reduction of nitrous oxide to dinitrogen by NosZ. We found that phylotypes I and III need NosZ for full virulence. However, strains in phylotypes II and IV are highly virulent despite lacking NosZ. The ability to respire by reducing nitrate to nitrous oxide does not greatly enhance the growth of phylotype II and IV strains. These partial denitrifying strains reach high cell densities during plant infection and cause typical wilt disease. However, unlike phylotype I and III strains, partial denitrifiers cannot grow well under anaerobic conditions or form thick biofilms in culture or in tomato xylem vessels. Furthermore, aerotaxis assays show that strains from different phylotypes have different oxygen and nitrate preferences. Together, these results indicate that the RSSC contains two subgroups that occupy the same habitat but have evolved divergent energy metabolism strategies to exploit distinct metabolic niches in the xylem. |
format | Online Article Text |
id | pubmed-9973335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-99733352023-03-01 Plant-Pathogenic Ralstonia Phylotypes Evolved Divergent Respiratory Strategies and Behaviors To Thrive in Xylem Truchon, Alicia N. Dalsing, Beth L. Khokhani, Devanshi MacIntyre, April McDonald, Bradon R. Ailloud, Florent Klassen, Jonathan Gonzalez-Orta, Enid T. Currie, Cameron Prior, Philippe Lowe-Power, Tiffany M. Allen, Caitilyn mBio Research Article Bacterial pathogens in the Ralstonia solanacearum species complex (RSSC) infect the water-transporting xylem vessels of plants, causing bacterial wilt disease. Strains in RSSC phylotypes I and III can reduce nitrate to dinitrogen via complete denitrification. The four-step denitrification pathway enables bacteria to use inorganic nitrogen species as terminal electron acceptors, supporting their growth in oxygen-limited environments such as biofilms or plant xylem. Reduction of nitrate, nitrite, and nitric oxide all contribute to the virulence of a model phylotype I strain. However, little is known about the physiological role of the last denitrification step, the reduction of nitrous oxide to dinitrogen by NosZ. We found that phylotypes I and III need NosZ for full virulence. However, strains in phylotypes II and IV are highly virulent despite lacking NosZ. The ability to respire by reducing nitrate to nitrous oxide does not greatly enhance the growth of phylotype II and IV strains. These partial denitrifying strains reach high cell densities during plant infection and cause typical wilt disease. However, unlike phylotype I and III strains, partial denitrifiers cannot grow well under anaerobic conditions or form thick biofilms in culture or in tomato xylem vessels. Furthermore, aerotaxis assays show that strains from different phylotypes have different oxygen and nitrate preferences. Together, these results indicate that the RSSC contains two subgroups that occupy the same habitat but have evolved divergent energy metabolism strategies to exploit distinct metabolic niches in the xylem. American Society for Microbiology 2023-02-06 /pmc/articles/PMC9973335/ /pubmed/36744950 http://dx.doi.org/10.1128/mbio.03188-22 Text en Copyright © 2023 Truchon et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Truchon, Alicia N. Dalsing, Beth L. Khokhani, Devanshi MacIntyre, April McDonald, Bradon R. Ailloud, Florent Klassen, Jonathan Gonzalez-Orta, Enid T. Currie, Cameron Prior, Philippe Lowe-Power, Tiffany M. Allen, Caitilyn Plant-Pathogenic Ralstonia Phylotypes Evolved Divergent Respiratory Strategies and Behaviors To Thrive in Xylem |
title | Plant-Pathogenic Ralstonia Phylotypes Evolved Divergent Respiratory Strategies and Behaviors To Thrive in Xylem |
title_full | Plant-Pathogenic Ralstonia Phylotypes Evolved Divergent Respiratory Strategies and Behaviors To Thrive in Xylem |
title_fullStr | Plant-Pathogenic Ralstonia Phylotypes Evolved Divergent Respiratory Strategies and Behaviors To Thrive in Xylem |
title_full_unstemmed | Plant-Pathogenic Ralstonia Phylotypes Evolved Divergent Respiratory Strategies and Behaviors To Thrive in Xylem |
title_short | Plant-Pathogenic Ralstonia Phylotypes Evolved Divergent Respiratory Strategies and Behaviors To Thrive in Xylem |
title_sort | plant-pathogenic ralstonia phylotypes evolved divergent respiratory strategies and behaviors to thrive in xylem |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9973335/ https://www.ncbi.nlm.nih.gov/pubmed/36744950 http://dx.doi.org/10.1128/mbio.03188-22 |
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