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Histochemical Evidence for Nitrogen-Transfer Endosymbiosis in Non-Photosynthetic Cells of Leaves and Inflorescence Bracts of Angiosperms

SIMPLE SUMMARY: We used light and confocal microscopy to visualize bacteria in leaf and bract cells of more than 30 species in 18 families of seed plants. We detected chemical exchanges between intracellular bacteria and plant cells. We found that endophytic bacteria that show evidence of the transf...

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Autores principales: Micci, April, Zhang, Qiuwei, Chang, Xiaoqian, Kingsley, Kathryn, Park, Linsey, Chiaranunt, Peerapol, Strickland, Raquele, Velazquez, Fernando, Lindert, Sean, Elmore, Matthew, Vines, Philip L., Crane, Sharron, Irizarry, Ivelisse, Kowalski, Kurt P., Johnston-Monje, David, White, James F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9220352/
https://www.ncbi.nlm.nih.gov/pubmed/35741397
http://dx.doi.org/10.3390/biology11060876
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author Micci, April
Zhang, Qiuwei
Chang, Xiaoqian
Kingsley, Kathryn
Park, Linsey
Chiaranunt, Peerapol
Strickland, Raquele
Velazquez, Fernando
Lindert, Sean
Elmore, Matthew
Vines, Philip L.
Crane, Sharron
Irizarry, Ivelisse
Kowalski, Kurt P.
Johnston-Monje, David
White, James F.
author_facet Micci, April
Zhang, Qiuwei
Chang, Xiaoqian
Kingsley, Kathryn
Park, Linsey
Chiaranunt, Peerapol
Strickland, Raquele
Velazquez, Fernando
Lindert, Sean
Elmore, Matthew
Vines, Philip L.
Crane, Sharron
Irizarry, Ivelisse
Kowalski, Kurt P.
Johnston-Monje, David
White, James F.
author_sort Micci, April
collection PubMed
description SIMPLE SUMMARY: We used light and confocal microscopy to visualize bacteria in leaf and bract cells of more than 30 species in 18 families of seed plants. We detected chemical exchanges between intracellular bacteria and plant cells. We found that endophytic bacteria that show evidence of the transfer of nitrogen to plants are present in non-photosynthetic cells of leaves and bracts of diverse plant species. Nitrogen transfer from bacteria was observed in epidermal cells, various filamentous and glandular trichomes, and other non-photosynthetic cells. The most efficient of the nitrogen-transfer endosymbioses were seen to involve glandular trichomes, as seen in hops (Humulus lupulus) and hemp (Cannabis sativa). Trichome chemistry is hypothesized to function to scavenge oxygen around bacteria to facilitate nitrogen fixation. ABSTRACT: We used light and confocal microscopy to visualize bacteria in leaf and bract cells of more than 30 species in 18 families of seed plants. Through histochemical analysis, we detected hormones (including ethylene and nitric oxide), superoxide, and nitrogenous chemicals (including nitric oxide and nitrate) around bacteria within plant cells. Bacteria were observed in epidermal cells, various filamentous and glandular trichomes, and other non-photosynthetic cells. Most notably, bacteria showing nitrate formation based on histochemical staining were present in glandular trichomes of some dicots (e.g., Humulus lupulus and Cannabis sativa). Glandular trichome chemistry is hypothesized to function to scavenge oxygen around bacteria and reduce oxidative damage to intracellular bacterial cells. Experiments to assess the differential absorption of isotopic nitrogen into plants suggest the assimilation of nitrogen into actively growing tissues of plants, where bacteria are most active and carbohydrates are more available. The leaf and bract cell endosymbiosis types outlined in this paper have not been previously reported and may be important in facilitating plant growth, development, oxidative stress resistance, and nutrient absorption into plants. It is unknown whether leaf and bract cell endosymbioses are significant in increasing the nitrogen content of plants. From the experiments that we conducted, it is impossible to know whether plant trichomes evolved specifically as organs for nitrogen fixation or if, instead, trichomes are structures in which bacteria easily colonize and where some casual nitrogen transfer may occur between bacteria and plant cells. It is likely that the endosymbioses seen in leaves and bracts are less efficient than those of root nodules of legumes in similar plants. However, the presence of endosymbioses that yield nitrate in plants could confer a reduced need for soil nitrogen and constitute increased nitrogen-use efficiency, even if the actual amount of nitrogen transferred to plant cells is small. More research is needed to evaluate the importance of nitrogen transfer within leaf and bract cells of plants.
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spelling pubmed-92203522022-06-24 Histochemical Evidence for Nitrogen-Transfer Endosymbiosis in Non-Photosynthetic Cells of Leaves and Inflorescence Bracts of Angiosperms Micci, April Zhang, Qiuwei Chang, Xiaoqian Kingsley, Kathryn Park, Linsey Chiaranunt, Peerapol Strickland, Raquele Velazquez, Fernando Lindert, Sean Elmore, Matthew Vines, Philip L. Crane, Sharron Irizarry, Ivelisse Kowalski, Kurt P. Johnston-Monje, David White, James F. Biology (Basel) Article SIMPLE SUMMARY: We used light and confocal microscopy to visualize bacteria in leaf and bract cells of more than 30 species in 18 families of seed plants. We detected chemical exchanges between intracellular bacteria and plant cells. We found that endophytic bacteria that show evidence of the transfer of nitrogen to plants are present in non-photosynthetic cells of leaves and bracts of diverse plant species. Nitrogen transfer from bacteria was observed in epidermal cells, various filamentous and glandular trichomes, and other non-photosynthetic cells. The most efficient of the nitrogen-transfer endosymbioses were seen to involve glandular trichomes, as seen in hops (Humulus lupulus) and hemp (Cannabis sativa). Trichome chemistry is hypothesized to function to scavenge oxygen around bacteria to facilitate nitrogen fixation. ABSTRACT: We used light and confocal microscopy to visualize bacteria in leaf and bract cells of more than 30 species in 18 families of seed plants. Through histochemical analysis, we detected hormones (including ethylene and nitric oxide), superoxide, and nitrogenous chemicals (including nitric oxide and nitrate) around bacteria within plant cells. Bacteria were observed in epidermal cells, various filamentous and glandular trichomes, and other non-photosynthetic cells. Most notably, bacteria showing nitrate formation based on histochemical staining were present in glandular trichomes of some dicots (e.g., Humulus lupulus and Cannabis sativa). Glandular trichome chemistry is hypothesized to function to scavenge oxygen around bacteria and reduce oxidative damage to intracellular bacterial cells. Experiments to assess the differential absorption of isotopic nitrogen into plants suggest the assimilation of nitrogen into actively growing tissues of plants, where bacteria are most active and carbohydrates are more available. The leaf and bract cell endosymbiosis types outlined in this paper have not been previously reported and may be important in facilitating plant growth, development, oxidative stress resistance, and nutrient absorption into plants. It is unknown whether leaf and bract cell endosymbioses are significant in increasing the nitrogen content of plants. From the experiments that we conducted, it is impossible to know whether plant trichomes evolved specifically as organs for nitrogen fixation or if, instead, trichomes are structures in which bacteria easily colonize and where some casual nitrogen transfer may occur between bacteria and plant cells. It is likely that the endosymbioses seen in leaves and bracts are less efficient than those of root nodules of legumes in similar plants. However, the presence of endosymbioses that yield nitrate in plants could confer a reduced need for soil nitrogen and constitute increased nitrogen-use efficiency, even if the actual amount of nitrogen transferred to plant cells is small. More research is needed to evaluate the importance of nitrogen transfer within leaf and bract cells of plants. MDPI 2022-06-07 /pmc/articles/PMC9220352/ /pubmed/35741397 http://dx.doi.org/10.3390/biology11060876 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Micci, April
Zhang, Qiuwei
Chang, Xiaoqian
Kingsley, Kathryn
Park, Linsey
Chiaranunt, Peerapol
Strickland, Raquele
Velazquez, Fernando
Lindert, Sean
Elmore, Matthew
Vines, Philip L.
Crane, Sharron
Irizarry, Ivelisse
Kowalski, Kurt P.
Johnston-Monje, David
White, James F.
Histochemical Evidence for Nitrogen-Transfer Endosymbiosis in Non-Photosynthetic Cells of Leaves and Inflorescence Bracts of Angiosperms
title Histochemical Evidence for Nitrogen-Transfer Endosymbiosis in Non-Photosynthetic Cells of Leaves and Inflorescence Bracts of Angiosperms
title_full Histochemical Evidence for Nitrogen-Transfer Endosymbiosis in Non-Photosynthetic Cells of Leaves and Inflorescence Bracts of Angiosperms
title_fullStr Histochemical Evidence for Nitrogen-Transfer Endosymbiosis in Non-Photosynthetic Cells of Leaves and Inflorescence Bracts of Angiosperms
title_full_unstemmed Histochemical Evidence for Nitrogen-Transfer Endosymbiosis in Non-Photosynthetic Cells of Leaves and Inflorescence Bracts of Angiosperms
title_short Histochemical Evidence for Nitrogen-Transfer Endosymbiosis in Non-Photosynthetic Cells of Leaves and Inflorescence Bracts of Angiosperms
title_sort histochemical evidence for nitrogen-transfer endosymbiosis in non-photosynthetic cells of leaves and inflorescence bracts of angiosperms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9220352/
https://www.ncbi.nlm.nih.gov/pubmed/35741397
http://dx.doi.org/10.3390/biology11060876
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