A Shoot Endosymbiont Colonizes Pine Host By Unique And Rhizobia-Like Mechanisms Boosted By Surface-Fixed Methanol
Koskimäki, Janne J; Pohjanen, Johanna; Ihantola, Emmi-Leena; Sutela, Suvi; Pirttilä, Anna Maria (2025-10-24)
Koskimäki, Janne J
Pohjanen, Johanna
Ihantola, Emmi-Leena
Sutela, Suvi
Pirttilä, Anna Maria
Oxford University Press
24.10.2025
Janne J Koskimäki, Johanna Pohjanen, Emmi-Leena Ihantola, Suvi Sutela, Anna Maria Pirttilä, A shoot endosymbiont colonizes pine host by unique and rhizobia-like mechanisms boosted by surface-fixed methanol, Plant and Cell Physiology, Volume 67, Issue 1, January 2026, Pages 39–54, https://doi.org/10.1093/pcp/pcaf135
https://creativecommons.org/licenses/by/4.0/
© The Author(s) 2025. Published by Oxford University Press on behalf of the Japanese Society of Plant Physiologists. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
https://creativecommons.org/licenses/by/4.0/
© The Author(s) 2025. Published by Oxford University Press on behalf of the Japanese Society of Plant Physiologists. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
https://creativecommons.org/licenses/by/4.0/
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:oulu-202511046572
https://urn.fi/URN:NBN:fi:oulu-202511046572
Tiivistelmä
Abstract
Methylorubrum extorquens DSM13060 (Rhizobiales) has a specific capacity to live inside cells of bud meristems in pine trees. The bud niche is almost completely unstudied, although likely widespread in plants. It is unknown how the endosymbiotic methylotroph enters such crucial tissues of the plant. We hypothesized the bud colonization to occur mainly through the shoot epidermis enabled by host-produced methanol. We combined several microscopic methods to illustrate spatio-temporal colonization dynamics and methanol utilization by M. extorquens DSM13060 during the interaction. Our results showed that the endosymbiont mainly enters pine seedlings through cylindrical sheath, which is a layer of living cells surrounding primary root and transition zone. The cylindrical sheath played a central role in accumulation and proliferation of bacteria before entering deeper tissues. The endosymbiont also penetrated host through epidermis and stomatal apertures in stem and formed infection pocket-like structures upon entry. M. extorquens DSM13060 activated the mxaF-promoter on plant surfaces for methanol assimilation prior to shifting to the endosymbiotic lifestyle. Our results suggest that the surface-bound methanol was used for production of antioxidants that enable tissue penetration, documented earlier. Gradual cell-to-cell passage or formation of intracellular infection threads enabled the invasion past endodermis into the xylem. The xylem was observed to function as the main route to the apical meristem, where bacteria were present after 90 days of inoculation. Our study widens the previously known niches and reveals unique and rhizobia-like colonization mechanisms by the endosymbiont in the above and below-ground parts of pine.
Methylorubrum extorquens DSM13060 (Rhizobiales) has a specific capacity to live inside cells of bud meristems in pine trees. The bud niche is almost completely unstudied, although likely widespread in plants. It is unknown how the endosymbiotic methylotroph enters such crucial tissues of the plant. We hypothesized the bud colonization to occur mainly through the shoot epidermis enabled by host-produced methanol. We combined several microscopic methods to illustrate spatio-temporal colonization dynamics and methanol utilization by M. extorquens DSM13060 during the interaction. Our results showed that the endosymbiont mainly enters pine seedlings through cylindrical sheath, which is a layer of living cells surrounding primary root and transition zone. The cylindrical sheath played a central role in accumulation and proliferation of bacteria before entering deeper tissues. The endosymbiont also penetrated host through epidermis and stomatal apertures in stem and formed infection pocket-like structures upon entry. M. extorquens DSM13060 activated the mxaF-promoter on plant surfaces for methanol assimilation prior to shifting to the endosymbiotic lifestyle. Our results suggest that the surface-bound methanol was used for production of antioxidants that enable tissue penetration, documented earlier. Gradual cell-to-cell passage or formation of intracellular infection threads enabled the invasion past endodermis into the xylem. The xylem was observed to function as the main route to the apical meristem, where bacteria were present after 90 days of inoculation. Our study widens the previously known niches and reveals unique and rhizobia-like colonization mechanisms by the endosymbiont in the above and below-ground parts of pine.
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