Plant-like bacterial expansins play contrasting roles in two tomato vascular pathogens
Expansin proteins, which loosen plant cell walls, play critical roles in normal plant growth and development. The horizontal acquisition of functional plant‐like expansin genes in numerous xylem‐colonizing phytopathogenic bacteria suggests that bacterial expansins may also contribute to virulence. T...
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sg-ntu-dr.10356-1376572023-02-28T17:07:22Z Plant-like bacterial expansins play contrasting roles in two tomato vascular pathogens Tancos, Matthew A. Lowe-Power, Tiffany M. Peritore-Galve, F. Christopher Tran, Tuan Minh Allen, Caitilyn Smart, Christine D. School of Biological Sciences Science::Biological sciences Bacterial Plant Pathogenesis Clavibacter Michiganensis Expansin proteins, which loosen plant cell walls, play critical roles in normal plant growth and development. The horizontal acquisition of functional plant‐like expansin genes in numerous xylem‐colonizing phytopathogenic bacteria suggests that bacterial expansins may also contribute to virulence. To investigate the role of bacterial expansins in plant diseases, we mutated the non‐chimeric expansin genes (CmEXLX2 and RsEXLX) of two xylem‐inhabiting bacterial pathogens, the Actinobacterium Clavibacter michiganensis ssp. michiganensis (Cmm) and the β‐proteobacterium Ralstonia solanacearum (Rs), respectively. The Cmm ΔCmEXLX2 mutant caused increased symptom development on tomato, which was characterized by more rapid wilting, greater vascular necrosis and abundant atypical lesions on distant petioles. This increased disease severity correlated with larger in planta populations of the ΔCmEXLX2 mutant, even though the strains grew as well as the wild‐type in vitro. Similarly, when inoculated onto tomato fruit, ΔCmEXLX2 caused significantly larger lesions with larger necrotic centres. In contrast, the Rs ΔRsEXLX mutant showed reduced virulence on tomato following root inoculation, but not following direct petiole inoculation, suggesting that the RsEXLX expansin contributes to early virulence at the root infection stage. Consistent with this finding, ΔRsEXLX attached to tomato seedling roots better than the wild‐type Rs, which may prevent mutants from invading the plant's vasculature. These contrasting results demonstrate the diverse roles of non‐chimeric bacterial expansins and highlight their importance in plant–bacterial interactions. Published version 2020-04-08T01:37:40Z 2020-04-08T01:37:40Z 2018 Journal Article Tancos, M. A., Lowe‐Power, T. M., Peritore‐Galve, F. C., Tran, T. M., Allen, C., & Smart, C. D. (2018). Plant‐like bacterial expansins play contrasting roles in two tomato vascular pathogens. Molecular Plant Pathology, 19(5), 1210-1221. doi:10.1111/mpp.12611 1464-6722 https://hdl.handle.net/10356/137657 10.1111/mpp.12611 28868644 2-s2.0-85038085134 5 19 1210 1221 en Molecular Plant Pathology © 2017 BSPP and John Wiley & Sons Ltd. This is an open-access article distributed under the terms of the Creative Commons Attribution License. application/pdf |
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Science::Biological sciences Bacterial Plant Pathogenesis Clavibacter Michiganensis Tancos, Matthew A. Lowe-Power, Tiffany M. Peritore-Galve, F. Christopher Tran, Tuan Minh Allen, Caitilyn Smart, Christine D. Plant-like bacterial expansins play contrasting roles in two tomato vascular pathogens |
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Expansin proteins, which loosen plant cell walls, play critical roles in normal plant growth and development. The horizontal acquisition of functional plant‐like expansin genes in numerous xylem‐colonizing phytopathogenic bacteria suggests that bacterial expansins may also contribute to virulence. To investigate the role of bacterial expansins in plant diseases, we mutated the non‐chimeric expansin genes (CmEXLX2 and RsEXLX) of two xylem‐inhabiting bacterial pathogens, the Actinobacterium Clavibacter michiganensis ssp. michiganensis (Cmm) and the β‐proteobacterium Ralstonia solanacearum (Rs), respectively. The Cmm ΔCmEXLX2 mutant caused increased symptom development on tomato, which was characterized by more rapid wilting, greater vascular necrosis and abundant atypical lesions on distant petioles. This increased disease severity correlated with larger in planta populations of the ΔCmEXLX2 mutant, even though the strains grew as well as the wild‐type in vitro. Similarly, when inoculated onto tomato fruit, ΔCmEXLX2 caused significantly larger lesions with larger necrotic centres. In contrast, the Rs ΔRsEXLX mutant showed reduced virulence on tomato following root inoculation, but not following direct petiole inoculation, suggesting that the RsEXLX expansin contributes to early virulence at the root infection stage. Consistent with this finding, ΔRsEXLX attached to tomato seedling roots better than the wild‐type Rs, which may prevent mutants from invading the plant's vasculature. These contrasting results demonstrate the diverse roles of non‐chimeric bacterial expansins and highlight their importance in plant–bacterial interactions. |
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School of Biological Sciences |
author_facet |
School of Biological Sciences Tancos, Matthew A. Lowe-Power, Tiffany M. Peritore-Galve, F. Christopher Tran, Tuan Minh Allen, Caitilyn Smart, Christine D. |
format |
Article |
author |
Tancos, Matthew A. Lowe-Power, Tiffany M. Peritore-Galve, F. Christopher Tran, Tuan Minh Allen, Caitilyn Smart, Christine D. |
author_sort |
Tancos, Matthew A. |
title |
Plant-like bacterial expansins play contrasting roles in two tomato vascular pathogens |
title_short |
Plant-like bacterial expansins play contrasting roles in two tomato vascular pathogens |
title_full |
Plant-like bacterial expansins play contrasting roles in two tomato vascular pathogens |
title_fullStr |
Plant-like bacterial expansins play contrasting roles in two tomato vascular pathogens |
title_full_unstemmed |
Plant-like bacterial expansins play contrasting roles in two tomato vascular pathogens |
title_sort |
plant-like bacterial expansins play contrasting roles in two tomato vascular pathogens |
publishDate |
2020 |
url |
https://hdl.handle.net/10356/137657 |
_version_ |
1759853751827431424 |