Rhizospheric and Endophytic Microbial Communities Associated with Leptadenia pyrotechnica in Arid Zones

Desert plants host specialized microbiomes that contribute to their survival under extreme conditions; yet, niche and specific microbial dynamics remain poorly understood. In this study, we used 16S rRNA amplicon sequencing to characterize the bacterial communities associated with Leptadenia pyrotechnica, which is a desert-adapted shrub. Five representative sample types were analyzed: rhizospheric soil from a non-arid adjacent location (control; S1); rhizospheric soil from the arid site (S4); and stem endosphere from the arid site (S5, S6, and S7). For each sample type, three biological replicates were collected from different healthy plants to ensure independence. Sequencing yielded high-quality datasets (89,000-134,000 reads/sample) with ASV retention ratios of 68-80%, confirming their sufficient depth for diversity profiling. Alpha diversity indices revealed a markedly greater richness in rhizospheric samples (e.g., S1 Shannon: 3.04; 530 ASVs) than in endosphere samples (Shannon < 1.0; ASVs ≤ 33), consistent with known gradients in desert plant microbiomes. Rarefaction curves confirmed the completeness of sampling. Beta diversity analyses, including PCoA and hierarchical clustering, showed clear segregation between rhizospheric and endophytic communities, indicating strong compartment-specific structuring. The rhizosphere was dominated by Actinobacteria (48%), Proteobacteria (32%), and Firmicutes (10%), whereas the stem endosphere was enriched in Proteobacteria (45%) and Actinobacteria (40%). Taxonomic profiling revealed that Bacillota and Actinomycetota dominated rhizospheric soils, including Bacillus licheniformis, while stem tissues were enriched in Cyanobacteriota and Alphaproteobacteria, suggesting host-driven filtering. Genera such as Cupriavidus, Massilia, and Noviherbaspirillum were exclusive to the rhizosphere, while Paracholeplasma appeared uniquely in stem sample S6. Archaea and rare phyla were nearly absent. The current findings indicate that L. pyrotechnica harbors distinct microbial assemblages in rhizospheric and endophytic niches, reflecting microhabitat-driven selection. These microbial communities may contribute to host resilience by harboring taxa with potential stress-tolerance traits, offering insights for microbiome-informed strategies in arid land restoration.