Breed Selection of Poplars Imposes Greater Selection Pressure on the Rhizosphere Bacterial Community
Breed selection alters the coevolution of plant–microbiome associations that have developed over long periods of natural evolution. We investigated the effects of breed selection on the rhizosphere microbiomes and metabolites of hybrid parents (I101 and 84K) and their offspring (Q1–Q5) using metagen...
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2024-10-01
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author | Jinliang Liu Long Zhou Yan Lan Junfeng Fan |
author_facet | Jinliang Liu Long Zhou Yan Lan Junfeng Fan |
author_sort | Jinliang Liu |
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description | Breed selection alters the coevolution of plant–microbiome associations that have developed over long periods of natural evolution. We investigated the effects of breed selection on the rhizosphere microbiomes and metabolites of hybrid parents (I101 and 84K) and their offspring (Q1–Q5) using metagenomics and untargeted metabolomics. Rhizosphere archaeal, bacterial and fungal community β-diversity significantly differed among hybrid parents and offspring, but only the dominant bacterial phyla and bacterial community α-diversity revealed significant differences. Approximately 5.49%, 14.90% and 7.86% of the archaeal, bacterial and fungal species significantly differed among the poplar hybrid parents and offspring. Rhizosphere microbial functional genes and metabolites were both clustered into the following three groups: I101 and 84K; Q2 and Q4; and Q1, Q3 and Q5. Compared with the hybrid parents, 15 phytochemical compounds were enriched in the hybrid offspring and explained 7.15%, 18.24% and 6.68% of the total variation in the archaeal, bacterial and fungal community compositions, respectively. Rhizosphere metabolites significantly affected the bacterial community, rather than the archaeal and fungal communities. Our observations suggested that poplar breed selection imposed greater selection pressure on the rhizosphere bacterial community, which was mainly driven by metabolites. |
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id | doaj-art-c0dfda23ed0c4d4983d9f30dba454ac4 |
institution | Kabale University |
issn | 2076-2607 |
language | English |
publishDate | 2024-10-01 |
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spelling | doaj-art-c0dfda23ed0c4d4983d9f30dba454ac42024-11-26T18:14:24ZengMDPI AGMicroorganisms2076-26072024-10-011211217610.3390/microorganisms12112176Breed Selection of Poplars Imposes Greater Selection Pressure on the Rhizosphere Bacterial CommunityJinliang Liu0Long Zhou1Yan Lan2Junfeng Fan3Key Laboratory of Silviculture on the Loess Plateau State Forestry Administration, College of Forestry, Northwest A&F University, Xianyang 712100, ChinaKey Laboratory of Silviculture on the Loess Plateau State Forestry Administration, College of Forestry, Northwest A&F University, Xianyang 712100, ChinaKey Laboratory of Silviculture on the Loess Plateau State Forestry Administration, College of Forestry, Northwest A&F University, Xianyang 712100, ChinaKey Laboratory of Silviculture on the Loess Plateau State Forestry Administration, College of Forestry, Northwest A&F University, Xianyang 712100, ChinaBreed selection alters the coevolution of plant–microbiome associations that have developed over long periods of natural evolution. We investigated the effects of breed selection on the rhizosphere microbiomes and metabolites of hybrid parents (I101 and 84K) and their offspring (Q1–Q5) using metagenomics and untargeted metabolomics. Rhizosphere archaeal, bacterial and fungal community β-diversity significantly differed among hybrid parents and offspring, but only the dominant bacterial phyla and bacterial community α-diversity revealed significant differences. Approximately 5.49%, 14.90% and 7.86% of the archaeal, bacterial and fungal species significantly differed among the poplar hybrid parents and offspring. Rhizosphere microbial functional genes and metabolites were both clustered into the following three groups: I101 and 84K; Q2 and Q4; and Q1, Q3 and Q5. Compared with the hybrid parents, 15 phytochemical compounds were enriched in the hybrid offspring and explained 7.15%, 18.24% and 6.68% of the total variation in the archaeal, bacterial and fungal community compositions, respectively. Rhizosphere metabolites significantly affected the bacterial community, rather than the archaeal and fungal communities. Our observations suggested that poplar breed selection imposed greater selection pressure on the rhizosphere bacterial community, which was mainly driven by metabolites.https://www.mdpi.com/2076-2607/12/11/2176breed selectionrhizosphere microbiomesuntargeted metabolomicspoplar |
spellingShingle | Jinliang Liu Long Zhou Yan Lan Junfeng Fan Breed Selection of Poplars Imposes Greater Selection Pressure on the Rhizosphere Bacterial Community Microorganisms breed selection rhizosphere microbiomes untargeted metabolomics poplar |
title | Breed Selection of Poplars Imposes Greater Selection Pressure on the Rhizosphere Bacterial Community |
title_full | Breed Selection of Poplars Imposes Greater Selection Pressure on the Rhizosphere Bacterial Community |
title_fullStr | Breed Selection of Poplars Imposes Greater Selection Pressure on the Rhizosphere Bacterial Community |
title_full_unstemmed | Breed Selection of Poplars Imposes Greater Selection Pressure on the Rhizosphere Bacterial Community |
title_short | Breed Selection of Poplars Imposes Greater Selection Pressure on the Rhizosphere Bacterial Community |
title_sort | breed selection of poplars imposes greater selection pressure on the rhizosphere bacterial community |
topic | breed selection rhizosphere microbiomes untargeted metabolomics poplar |
url | https://www.mdpi.com/2076-2607/12/11/2176 |
work_keys_str_mv | AT jinliangliu breedselectionofpoplarsimposesgreaterselectionpressureontherhizospherebacterialcommunity AT longzhou breedselectionofpoplarsimposesgreaterselectionpressureontherhizospherebacterialcommunity AT yanlan breedselectionofpoplarsimposesgreaterselectionpressureontherhizospherebacterialcommunity AT junfengfan breedselectionofpoplarsimposesgreaterselectionpressureontherhizospherebacterialcommunity |