Rhizosphere microorganisms play a vital role in enhancing plant health, productivity, and the accumulation of secondary metabolites. Currently, there is a limited understanding of the ecological processes that control the assembly of community. To address the role of microbial interactions in assembly and for functioning of the rhizosphere soil microbiota, we collected rhizosphere soil samples from Anisodus tanguticus on the Tibetan Plateau spanning 1500 kilometers, and sequenced the bacteria, fungi, archaea, and protist communities. We observed a significant but weak distance-decay relationship in the microbial communities of rhizosphere soil. Our comprehensive analysis of spatial, abiotic, and biotic factors showed that trophic relationships between protists and bacteria and fungi predominantly influenced the alpha and beta diversity of bacterial, fungal, and protistan communities, while abiotic factors had a greater impact on archaeal communities, including soil pH, available phosphorus, total phosphorus and mean annual temperature. Importantly, microbial interactions had a more significant influence on Anisodus tanguticus physiological and ecological functions compared to individual microorganisms. Network analyses revealed that bacteria occupy a central position of the co-occurrence network and play a crucial role of connector within this community. The addition of protists increased the stability of bacterial, fungal, and archaeal networks. Overall, our findings indicate that trophic relationships play an important role in assembly and for functioning of the rhizosphere soil microbiota. Bacterial communities serve as a crucial link between different kingdoms of microorganisms in the rhizosphere community. These findings help us to fully harness the beneficial functions of rhizosphere microorganisms for plants and achieve sustainable use of biological resources.

As an important Tibetan medicine and a secondary protected plant in China, Pomatosace filicula is endemic to the country and is mainly distributed in the Qinghai–Tibet Plateau (QTP). However, global climate change caused by greenhouse gas emissions might lead to the extinction of P. filicula. To understand the potential spatial distribution of P. filicula in future global warming scenarios, we used the MaxEnt model to simulate changes in its suitable habitat that would occur by 2050 and 2070 using four representative concentration pathway (RCP) scenarios and five global climate models. The results showed that the QTP currently contains a suitable habitat for P. filicula and will continue to do so in the future. Under the RCP2.6 scenario, the suitable habitat area would increase by 2050 but shrink slightly by 2070, with an average reduction of 2.7%. However, under the RCP8.5 scenario, the area of unsuitable habitat would expand by an average of 54.65% and 68.20% by 2050 and 2070, respectively. The changes in the area of suitable habitat under the RCP4.5 and RCP6.0 scenarios were similar, with the unsuitable area increasing by approximately 20% by 2050 and 2070. Under these two moderate RCPs, the total suitable area in 2070 would be greater than that in 2050. The top three environmental factors impacting the habitat distribution were altitude, annual precipitation (BIO12) and annual temperature range (BIO7). The cumulative contribution rate of these three factors was as high as 82.8%, indicating that they were the key factors affecting the distribution and adaptability of P. filicula, P. filicula grows well in damp and cold environments. Due to global warming, the QTP will become warmer and drier; thus, the growing area of P. filicula will move toward higher elevations and areas that are humid and cold. These areas are mainly found near the Three-River Region. Future climate change will aggravate the deterioration of the P. filicula habitat and increase the species’ survival risk. This study describes the distribution of P. filicula and provides a basis for the protection of endangered plants in the QTP.

20-Hydroxyecdysone (20E) is known to have numerous pharmacological activities and can be used to treat diabetes and cardiovascular diseases. However, the protective effects of 20E against endothelial dysfunction and its targets remain unclear. In the present study, we revealed that 20E treatment could modulate the release of the endothelium-derived vasomotor factors NO, PGI₂ and ET-1 and suppress the expression of ACE in TNF-α-induced 3D-cultured HUVECs. In addition, 20E suppressed the expression of CD40 and promoted the expression of SIRT6 in TNF-α-induced 3D-cultured HUVECs. The cellular thermal shift assay (CETSA), drug affinity responsive target stability (DARTS) and molecular docking results demonstrated that 20E binding increased SIRT6 stability, indicating that 20E directly bound to SIRT6 in HUVECs. Further investigation of the underlying mechanism showed that 20E could upregulate SIRT6 levels and that SIRT6 knockdown abolished the regulatory effect of 20E on CD40 in TNF-α-induced HUVECs, while SIRT6 overexpression further improved the effect of 20E. Moreover, we found that 20E could reduce the acetylation of NF-κB p65 (K310) through SIRT6, but the catalytic inactive mutant SIRT6 (H133Y) did not promote the deacetylation of NF-κB p65, suggesting that the inhibitory effect of 20E on NF-κB p65 was dependent on SIRT6 deacetylase activity. Additionally, our results indicated that 20E inhibited NF-κB via SIRT6, and the expression of CD40 was increased in HUVECs treated with SIRT6 siRNA and NF-κB inhibitor. In conclusion, the present study demonstrates that 20E exerts its effect through SIRT6-mediated deacetylation of NF-κB p65 (K310) to inhibit CD40 expression in ECs, and 20E may have therapeutic potential for the treatment of cardiovascular diseases.