TY - JOUR
T1 - Uncovering the dominant role of root metabolism in shaping rhizosphere metabolome under drought in tropical rainforest plants
AU - Hildebrand, Gina A.
AU - Honeker, Linnea K.
AU - Freire-Zapata, Viviana
AU - Ayala-Ortiz, Christian
AU - Rajakaruna, Sumudu
AU - Fudyma, Jane
AU - Daber, L. Erik
AU - AminiTabrizi, Roya
AU - Chu, Rosalie L.
AU - Toyoda, Jason
AU - Flowers, Sarah E.
AU - Hoyt, David W.
AU - Hamdan, Rasha
AU - Gil-Loaiza, Juliana
AU - Shi, Lingling
AU - Dippold, Michaela A.
AU - Ladd, S. Nemiah
AU - Werner, Christiane
AU - Meredith, Laura K.
AU - Tfaily, Malak M.
N1 - Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/11/15
Y1 - 2023/11/15
N2 - Plant-soil-microbe interactions are crucial for driving rhizosphere processes that contribute to metabolite turnover and nutrient cycling. With the increasing frequency and severity of water scarcity due to climate warming, understanding how plant-mediated processes, such as root exudation, influence soil organic matter turnover in the rhizosphere is essential. In this study, we used 16S rRNA gene amplicon sequencing, rhizosphere metabolomics, and position-specific 13C-pyruvate labeling to examine the effects of three different plant species (Piper auritum, Hibiscus rosa sinensis, and Clitoria fairchildiana) and their associated microbial communities on soil organic carbon turnover in the rhizosphere. Our findings indicate that in these tropical plants, the rhizosphere metabolome is primarily shaped by the response of roots to drought rather than direct shifts in the rhizosphere bacterial community composition. Specifically, the reduced exudation of plant roots had a notable effect on the metabolome of the rhizosphere of P. auritum, with less reliance on neighboring microbes. Contrary to P. auritum, H. rosa sinensis and C. fairchildiana experienced changes in their exudate composition during drought, causing alterations to the bacterial communities in the rhizosphere. This, in turn, had a collective impact on the rhizosphere's metabolome. Furthermore, the exclusion of phylogenetically distant microbes from the rhizosphere led to shifts in its metabolome. Additionally, C. fairchildiana appeared to be associated with only a subset of symbiotic bacteria under drought conditions. These results indicate that plant species-specific microbial interactions systematically change with the root metabolome. As roots respond to drought, their associated microbial communities adapt, potentially reinforcing the drought tolerance strategies of plant roots. These findings have significant implications for maintaining plant health and preference during drought stress and improving plant performance under climate change.
AB - Plant-soil-microbe interactions are crucial for driving rhizosphere processes that contribute to metabolite turnover and nutrient cycling. With the increasing frequency and severity of water scarcity due to climate warming, understanding how plant-mediated processes, such as root exudation, influence soil organic matter turnover in the rhizosphere is essential. In this study, we used 16S rRNA gene amplicon sequencing, rhizosphere metabolomics, and position-specific 13C-pyruvate labeling to examine the effects of three different plant species (Piper auritum, Hibiscus rosa sinensis, and Clitoria fairchildiana) and their associated microbial communities on soil organic carbon turnover in the rhizosphere. Our findings indicate that in these tropical plants, the rhizosphere metabolome is primarily shaped by the response of roots to drought rather than direct shifts in the rhizosphere bacterial community composition. Specifically, the reduced exudation of plant roots had a notable effect on the metabolome of the rhizosphere of P. auritum, with less reliance on neighboring microbes. Contrary to P. auritum, H. rosa sinensis and C. fairchildiana experienced changes in their exudate composition during drought, causing alterations to the bacterial communities in the rhizosphere. This, in turn, had a collective impact on the rhizosphere's metabolome. Furthermore, the exclusion of phylogenetically distant microbes from the rhizosphere led to shifts in its metabolome. Additionally, C. fairchildiana appeared to be associated with only a subset of symbiotic bacteria under drought conditions. These results indicate that plant species-specific microbial interactions systematically change with the root metabolome. As roots respond to drought, their associated microbial communities adapt, potentially reinforcing the drought tolerance strategies of plant roots. These findings have significant implications for maintaining plant health and preference during drought stress and improving plant performance under climate change.
KW - Drought
KW - Primary and secondary metabolites
KW - Pyruvate
KW - Rhizosphere
KW - Roots
KW - Tropical rainforest
UR - http://www.scopus.com/inward/record.url?scp=85166001141&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85166001141&partnerID=8YFLogxK
U2 - 10.1016/j.scitotenv.2023.165689
DO - 10.1016/j.scitotenv.2023.165689
M3 - Article
C2 - 37481084
AN - SCOPUS:85166001141
SN - 0048-9697
VL - 899
JO - Science of the Total Environment
JF - Science of the Total Environment
M1 - 165689
ER -