The circadian clock regulates plant metabolic functions and is an important component in plant health and productivity. Rhizosphere bacteria play critical roles in plant growth, health, and development and are shaped primarily by soil communities. Using Illumina next-generation sequencing, we characterized bacterial communities of wild-type (Col-0) Arabidopsis thaliana and an acyclic line (OX34) ectopically expressing the CCA1 transcription factor, relative to a soil control. Significantly different bacterial community structures (P = 0.031) were observed in the rhizosphere of wild-type plants between light and dark cycle samples. Furthermore, 13% of the community showed cycling, with abundances of several families, including Burkholderiaceae, Rhodospirillaceae, Planctomycetaceae, and Gaiellaceae, exhibiting fluctuation in abundances relative to the light cycle. However, limited-to-no cycling was observed in the acyclic CCAox34 line or soil controls. Functional gene inference revealed that genes involved in carbohydrate metabolism were likely more abundant in near-dawn, dark samples. Additionally, the composition of organic matter in the rhizosphere showed a significant variation between dark and light cycles. The results of this study suggest that the rhizosphere bacterial community is regulated to some extent by the circadian clock and is likely influenced by and exerts influences on plant metabolism and productivity. The timing of bacterial cycling in relation to that of Arabidopsis further suggests that diurnal dynamics influence plant-microbe carbon metabolism and exchange. Equally important, our study suggests that previous studies done without relevance to time of day need to be re-evaluated with regard to the impact of diurnal cycles on the rhizosphere microbial community.
Revised: January 29, 2021 |
Published: June 24, 2017
Citation
Staley C., A.P. Ferrieri, M.M. Tfaily, Y. Cui, R.K. Chu, P. Wang, and J.B. Shaw, et al. 2017.Diurnal Cycling of Rhizosphere Bacterial Communities is Associated with Shifts in Carbon Metabolism.Microbiome 5.PNNL-SA-121718.doi:10.1186/s40168-017-0287-1