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Plant Growth Promotion Diversity in Switchgrass-Colonizing, Diazotrophic Endophytes

Endophytic nitrogen-fixing (diazotrophic) bacteria are essential members of the microbiome of switchgrass (Panicum virgatum), considered to be an important commodity crop in bioenergy production. While endophytic diazotrophs are known to provide fixed atmospheric nitrogen to their host plant, there...

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Autores principales: Gushgari-Doyle, Sara, Schicklberger, Marcus, Li, Yifan V., Walker, Robert, Chakraborty, Romy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633415/
https://www.ncbi.nlm.nih.gov/pubmed/34867848
http://dx.doi.org/10.3389/fmicb.2021.730440
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author Gushgari-Doyle, Sara
Schicklberger, Marcus
Li, Yifan V.
Walker, Robert
Chakraborty, Romy
author_facet Gushgari-Doyle, Sara
Schicklberger, Marcus
Li, Yifan V.
Walker, Robert
Chakraborty, Romy
author_sort Gushgari-Doyle, Sara
collection PubMed
description Endophytic nitrogen-fixing (diazotrophic) bacteria are essential members of the microbiome of switchgrass (Panicum virgatum), considered to be an important commodity crop in bioenergy production. While endophytic diazotrophs are known to provide fixed atmospheric nitrogen to their host plant, there are many other plant growth-promoting (PGP) capabilities of these organisms to be demonstrated. The diversity of PGP traits across different taxa of switchgrass-colonizing endophytes is understudied, yet critical for understanding endophytic function and improving cultivation methods of important commodity crops. Here, we present the isolation and characterization of three diazotrophic endophytes: Azospirillum agricola R1C, Klebsiella variicola F10Cl, and Raoultella terrigena R1Gly. Strains R1C and F10Cl were isolated from switchgrass and strain R1Gly, while isolated from tobacco, is demonstrated herein to colonize switchgrass. Each strain exhibited highly diverse genomic and phenotypic PGP capabilities. Strain F10Cl and R1Gly demonstrated the highest functional similarity, suggesting that, while endophyte community structure may vary widely based on host species, differences in functional diversity are not a clearly delineated. The results of this study advance our understanding of diazotrophic endophyte diversity, which will allow us to design robust strategies to improve cultivation methods of many economically important commodity crops.
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spelling pubmed-86334152021-12-02 Plant Growth Promotion Diversity in Switchgrass-Colonizing, Diazotrophic Endophytes Gushgari-Doyle, Sara Schicklberger, Marcus Li, Yifan V. Walker, Robert Chakraborty, Romy Front Microbiol Microbiology Endophytic nitrogen-fixing (diazotrophic) bacteria are essential members of the microbiome of switchgrass (Panicum virgatum), considered to be an important commodity crop in bioenergy production. While endophytic diazotrophs are known to provide fixed atmospheric nitrogen to their host plant, there are many other plant growth-promoting (PGP) capabilities of these organisms to be demonstrated. The diversity of PGP traits across different taxa of switchgrass-colonizing endophytes is understudied, yet critical for understanding endophytic function and improving cultivation methods of important commodity crops. Here, we present the isolation and characterization of three diazotrophic endophytes: Azospirillum agricola R1C, Klebsiella variicola F10Cl, and Raoultella terrigena R1Gly. Strains R1C and F10Cl were isolated from switchgrass and strain R1Gly, while isolated from tobacco, is demonstrated herein to colonize switchgrass. Each strain exhibited highly diverse genomic and phenotypic PGP capabilities. Strain F10Cl and R1Gly demonstrated the highest functional similarity, suggesting that, while endophyte community structure may vary widely based on host species, differences in functional diversity are not a clearly delineated. The results of this study advance our understanding of diazotrophic endophyte diversity, which will allow us to design robust strategies to improve cultivation methods of many economically important commodity crops. Frontiers Media S.A. 2021-11-12 /pmc/articles/PMC8633415/ /pubmed/34867848 http://dx.doi.org/10.3389/fmicb.2021.730440 Text en Copyright © 2021 Gushgari-Doyle, Schicklberger, Li, Walker and Chakraborty. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Gushgari-Doyle, Sara
Schicklberger, Marcus
Li, Yifan V.
Walker, Robert
Chakraborty, Romy
Plant Growth Promotion Diversity in Switchgrass-Colonizing, Diazotrophic Endophytes
title Plant Growth Promotion Diversity in Switchgrass-Colonizing, Diazotrophic Endophytes
title_full Plant Growth Promotion Diversity in Switchgrass-Colonizing, Diazotrophic Endophytes
title_fullStr Plant Growth Promotion Diversity in Switchgrass-Colonizing, Diazotrophic Endophytes
title_full_unstemmed Plant Growth Promotion Diversity in Switchgrass-Colonizing, Diazotrophic Endophytes
title_short Plant Growth Promotion Diversity in Switchgrass-Colonizing, Diazotrophic Endophytes
title_sort plant growth promotion diversity in switchgrass-colonizing, diazotrophic endophytes
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633415/
https://www.ncbi.nlm.nih.gov/pubmed/34867848
http://dx.doi.org/10.3389/fmicb.2021.730440
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