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Mousa" }, { "@type": "Person", "name": "Ruqaia AlShami" }, { "@type": "Person", "name": "Rose Ghemrawi" } ], "publisher": { "@type": "Organization", "name": "F1000Research", "logo": { "@type": "ImageObject", "url": "https://f1000research.com/img/AMP/F1000Research_image.png", "height": 480, "width": 60 } }, "image": { "@type": "ImageObject", "url": "https://f1000research.com/img/AMP/F1000Research_image.png", "height": 1200, "width": 150 }, "description": " Background Climate change is expanding arid regions globally, intensifying drought, salinity, and heat stress that threaten ecosystem stability and food security. Desert plants of the Arabian Peninsula have evolved physiological and microbial adaptations that enable survival under such extremes. This study investigates the endophytic microbial communities of four representative xerophytic species; Zygophyllum mandavillei, Tribulus zeyheri, Limeum arabicum, and Cyperus conglomeratus, to identify functional traits that promote their climatic resilience. These perennial species were selected because they inhabit similar arid environments and share xerophytic traits such as reduced leaf area, fibrous root systems, and high drought tolerance, making them ideal models for examining interactions between plants and their associated microbes in desert ecosystems. Methods High-throughput environmental DNA (eDNA) sequencing was performed on 27 plant samples, generating 3,660,664 high-quality reads. Taxonomic clustering resolved the sequences into 30 phyla, 15 classes, 20 orders, 27 families, and 21 genera. Diversity analyses were conducted to evaluate microbial richness and community structure, and functional inference was performed using PICRUSt2. Results Dominant microbial taxa included Alphaproteobacteria, Actinomycetia, Cyanophyceae, and Gammaproteobacteria, groups known for nitrogen fixation, carbon cycling, and resistance to desiccation and heat. Alpha-diversity analyses revealed significant variation in species richness among the host plants, while beta-diversity metrics showed distinct clustering patterns, indicating host-specific microbial assembly shaped by plant genotype and microhabitat. Functional prediction suggested enrichment of pathways related to amino acid, carbohydrate, and lipid metabolism, oxidative phosphorylation, DNA repair, and secondary-metabolite biosynthesis, supporting metabolic versatility and stress adaptation. Conclusions These findings provide a comprehensive genomic overview of endophytic bacterial communities associated with key desert plants of the Arabian Peninsula and establish a foundation for future functional validation and sustainable applications of desert microbiomes under climate change. " } { "@context": "http://schema.org", "@type": "BreadcrumbList", "itemListElement": [ { "@type": "ListItem", "position": "1", "item": { "@id": "https://f1000research.com/", "name": "Home" } }, { "@type": "ListItem", "position": "2", "item": { "@id": "https://f1000research.com/browse/articles", "name": "Browse" } }, { "@type": "ListItem", "position": "3", "item": { "@id": "https://f1000research.com/articles/15-9", "name": "Plant Microbiome of the Arabian Peninsula Desert Reveals Unique Structural..." } } ] } Home Browse Plant Microbiome of the Arabian Peninsula Desert Reveals Unique Structural... ALL Metrics - Views Downloads Get PDF Get XML Cite How to cite this article Mousa WK, AlShami R and Ghemrawi R. Plant Microbiome of the Arabian Peninsula Desert Reveals Unique Structural and Functional Adaptations Supporting Climate Resilience [version 1; peer review: 1 approved with reservations] . F1000Research 2026, 15 :9 ( https://doi.org/10.12688/f1000research.172949.1 ) NOTE: If applicable, it is important to ensure the information in square brackets after the title is included in all citations of this article. Close Copy Citation Details Export Export Citation Sciwheel EndNote Ref. Manager Bibtex ProCite Sente EXPORT Select a format first Track Share ▬ ✚ Research Article Plant Microbiome of the Arabian Peninsula Desert Reveals Unique Structural and Functional Adaptations Supporting Climate Resilience [version 1; peer review: 1 approved with reservations] Walaa K. Mousa https://orcid.org/0000-0003-3229-4499 1,2 , Ruqaia AlShami https://orcid.org/0009-0007-1097-0333 1 , Rose Ghemrawi https://orcid.org/0000-0002-2465-0812 1 Walaa K. Mousa https://orcid.org/0000-0003-3229-4499 1,2 , Ruqaia AlShami https://orcid.org/0009-0007-1097-0333 1 , Rose Ghemrawi https://orcid.org/0000-0002-2465-0812 1 PUBLISHED 06 Jan 2026 Author details Author details 1 Al Ain University College of Pharmacy, Al Ain, Abu Dhabi, United Arab Emirates 2 Department of Pharmacognosy, Faculty of Pharmacy, Mansoura University, Dakahlia Governorate, Egypt Walaa K. Mousa Roles: Conceptualization, Formal Analysis, Funding Acquisition, Methodology, Resources, Supervision, Writing – Review & Editing Ruqaia AlShami Roles: Formal Analysis, Methodology, Writing – Original Draft Preparation Rose Ghemrawi Roles: Formal Analysis, Writing – Review & Editing OPEN PEER REVIEW DETAILS REVIEWER STATUS This article is included in the Genomics and Genetics gateway. This article is included in the Climate gateway. Abstract Background Climate change is expanding arid regions globally, intensifying drought, salinity, and heat stress that threaten ecosystem stability and food security. Desert plants of the Arabian Peninsula have evolved physiological and microbial adaptations that enable survival under such extremes. This study investigates the endophytic microbial communities of four representative xerophytic species; Zygophyllum mandavillei, Tribulus zeyheri, Limeum arabicum, and Cyperus conglomeratus, to identify functional traits that promote their climatic resilience. These perennial species were selected because they inhabit similar arid environments and share xerophytic traits such as reduced leaf area, fibrous root systems, and high drought tolerance, making them ideal models for examining interactions between plants and their associated microbes in desert ecosystems. Methods High-throughput environmental DNA (eDNA) sequencing was performed on 27 plant samples, generating 3,660,664 high-quality reads. Taxonomic clustering resolved the sequences into 30 phyla, 15 classes, 20 orders, 27 families, and 21 genera. Diversity analyses were conducted to evaluate microbial richness and community structure, and functional inference was performed using PICRUSt2. Results Dominant microbial taxa included Alphaproteobacteria, Actinomycetia, Cyanophyceae, and Gammaproteobacteria, groups known for nitrogen fixation, carbon cycling, and resistance to desiccation and heat. Alpha-diversity analyses revealed significant variation in species richness among the host plants, while beta-diversity metrics showed distinct clustering patterns, indicating host-specific microbial assembly shaped by plant genotype and microhabitat. Functional prediction suggested enrichment of pathways related to amino acid, carbohydrate, and lipid metabolism, oxidative phosphorylation, DNA repair, and secondary-metabolite biosynthesis, supporting metabolic versatility and stress adaptation. Conclusions These findings provide a comprehensive genomic overview of endophytic bacterial communities associated with key desert plants of the Arabian Peninsula and establish a foundation for future functional validation and sustainable applications of desert microbiomes under climate change. READ ALL READ LESS Keywords Climate change, sustainability, functional genomics, beneficial microbes, Arabian Desert Corresponding Author(s) Walaa K. Mousa ( [email protected] ) Close Corresponding author: Walaa K. Mousa Competing interests: No competing interests were disclosed. Grant information: The research is supported by an external grant from Sandooq Al Watan organization, UAE to the PI, WKM. Project ID: PRJ-SWARD-711. Grant NO: SWARD-F23-020. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Copyright: © 2026 Mousa WK et al . This is an open access article distributed under the terms of the Creative Commons Attribution License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. How to cite: Mousa WK, AlShami R and Ghemrawi R. Plant Microbiome of the Arabian Peninsula Desert Reveals Unique Structural and Functional Adaptations Supporting Climate Resilience [version 1; peer review: 1 approved with reservations] . F1000Research 2026, 15 :9 ( https://doi.org/10.12688/f1000research.172949.1 ) First published: 06 Jan 2026, 15 :9 ( https://doi.org/10.12688/f1000research.172949.1 ) Latest published: 06 Jan 2026, 15 :9 ( https://doi.org/10.12688/f1000research.172949.1 ) Introduction Microorganisms inhabiting extreme environments, or extremophiles, have long served as models for studying the boundaries of life. They flourish in habitats once considered inhospitable, including icy polar regions, volcanic vents, acidic lakes, and arid deserts—through mechanisms such as specialized membrane lipids, molecular chaperones, metal resistance systems, and the production of protective pigments and exopolysaccharides ( Neilson et al., 2012 ; Feller, 2017 ; Vieille & Zeikus, 2001 ). For example, psychrophilic species synthesize antifreeze proteins and cold-active enzymes to maintain metabolic activity under freezing conditions. At the same time, thermophiles adapt to high temperatures through thermostable proteins and ether-linked membrane lipids ( Kates, 1992 ). Acidophiles such as Acidithiobacillus ferrooxidans resist toxic metal concentrations through efflux systems and biofilm formation ( Dopson & Holmes, 2014 ). Likewise, desert-adapted microorganisms synthesize carotenoids and melanins that protect against UV radiation and produce extracellular polysaccharides (EPS) to retain moisture and mitigate desiccation stress ( Cockell & Knowland, 1999 ; Sher et al., 2019 ). These mechanisms reflect evolutionary strategies that sustain microbial survival and support their host plant in the most arid habitats. In arid ecosystems, plants depend on their associated microbiota to tolerate abiotic stress and maintain productivity. The Arabian Peninsula is among the driest regions globally, hosting a limited number of highly adapted plant species that thrive under extreme temperature, salinity, and water scarcity. These plants exhibit physiological traits such as deep root systems, osmoprotectant accumulation, and efficient water-use strategies that allow persistence in nutrient-poor soils. However, their resilience is also shaped by intimate interactions with their endophytic microbiota, defined as microorganisms residing inside plant tissues without causing harm ( Alsharif et al., 2020 ). Endophytic bacteria enhance plant growth by producing phytohormones, solubilizing nutrients, and synthesizing bioactive metabolites that improve drought and salinity tolerance ( Fanai et al., 2024 ) They also contribute to nitrogen fixation and carbon cycling, processes vital for sustaining life in desert ecosystems where organic matter is limited ( Feiner et al., 2015 ). Despite their ecological and potential biotechnological importance, the desert plant microbiome, particularly endophytic communities, remains poorly characterized. Previous studies in other desert systems, such as the Atacama and Namib, revealed microbial lineages uniquely adapted to aridity and nutrient limitation ( Ronca et al., 2015 ) but similar research in the Arabian Peninsula is limited. Existing data on desert soils and rhizospheres provide limited insight into the microbiota living within plant tissues, which are likely to harbor distinct communities with specialized functional roles ( Turner et al., 2013 ). Understanding the structure and function of these plant-associated microbial communities is therefore critical to elucidating how desert plants persist under extreme abiotic stress and to identify microbial traits that can be leveraged to enhance agricultural resilience in drylands. Recent advances in culture-independent methods, particularly high-throughput 16S rRNA gene sequencing and metagenomic inference tools such as PICRUSt2, now enable comprehensive profiling of microbiomes across ecosystems ( Haryono et al., 2021 ). These tools allow simultaneous assessment of microbial diversity and prediction of metabolic pathways involved in nutrient metabolism, stress tolerance, and environmental detoxification. Applying such approaches to native desert plants can uncover microbial taxa and genes that facilitate survival in environments projected to expand under global warming. Moreover, desert-derived microbes have emerged as promising sources of enzymes, pigments, and osmoprotectants that could be harnessed for biotechnology and sustainable agriculture ( Ortiz et al., 2021 ). In this study, we investigated the endophytic bacterial communities associated with four desert plants native to the Arabian Peninsula namely Zygophyllum mandavillei, Tribulus zeyheri, Limeum arabicum, and Cyperus conglomeratus. Z. mandavillei is native to hyper-arid zones of the Arabian Peninsula and represents a model for studying drought tolerance and symbiotic adaptation ( Abdullah, 2017 ) T. zeyheri (Zygophyllaceae) is known to promote sand fixation and water conservation ( Khan et al., 2020 ). L. arabicum, native to the Arabian deserts, is known for its medicinal properties and tolerance to extreme aridity ( Khan et al., 2020 ). C. conglomeratus (Cyperaceae), abundant across the Middle East and North Africa, is valued for its anti-inflammatory properties and capacity to thrive in sandy and nutrient-poor soils ( Brown & Feulner, 2023 ). These plant systems collectively provide an ideal lens to study microbial resilience under increasing global aridification. Using 16S rRNA gene amplicon sequencing and functional inference analysis, we aimed to (1) characterize their microbial diversity and taxonomic composition, (2) identify dominant and unique taxa associated with each host plant, and (3) predict the metabolic pathways that enable microbial survival under extreme desert conditions. By linking microbial diversity with functional potential, this study reveals ecological strategies that support desert ecosystem resilience and demonstrates how native plant microbiomes can guide the development of microbial solutions for sustainability and climate adaptation. Material and methods Plant collection and sample preparation Four desert plant species native to the Arabian Peninsula namely Zygophyllum mandavillei, Tribulus zeyheri Sond., Limeum arabicum, and Cyperus conglomeratus Rottb. were selected for microbiome analysis, as these species are highly adapted to arid environments and play key roles in desert ecosystem stability. The plant material used in this study was identified by Dr Walaa Mousa. A voucher specimen was not deposited for this study because no new collection was made; the species is already maintained and documented at the UAE Plant Genetic Resource Centre, and live specimens of the same species are also demonstrated in the educational botanical garden in Al Ain City. During November 2024, plant material was collected from Al-Ain desert, United Arab Emirates (approximate coordinates: 24.20° N, 55.70° E). At each of five independent adjacent sites per plant species, 6-7 individual plants were sampled and then pooled to form one composite sample. Thus, for the four species across five sites, a total of 130 plant samples (4 species × 5 sites × 6-7 independent plant samples, each sample is a composite of 5 pooled subsamples) were obtained. Samples were placed in sterile polyethylene bags, transported on ice, and transitely stored at −20°C until further processing. Surface sterilization & DNA extraction Endophytic (endosphere) microbiota were analyzed following modifications of protocols by Coombs & Franco ( Coombs & Franco, 2003 ) and Edwards et al. ( Edwards et al., 1991 ). Plant tissue were surface-sterilized by immersion in 95% ethanol for 3 min, rinsed with sterile distilled water, immersed in 3% sodium hypochlorite for 5 min, followed by three sterile water rinses. Sterilization was repeated twice to ensure efficacy. To validate surface sterilization, 100 μL of the final rinse water was plated on tryptic soy agar (TSA) and incubated at 25°C and 37°C for 72 h; absence of colony growth confirmed sterilization. Sterile tissues were ground under liquid nitrogen, and total genomic DNA was extracted using the chloroform–isoamyl alcohol method ( Edwards et al., 1991 ). DNA quality was verified by 1% agarose gel electrophoresis and quantified using a NanoDrop™ spectrophotometer (Thermo Fisher Scientific, USA). PCR amplification of the 16S rRNA gene The V3–V4 hypervariable region of the bacterial 16S rRNA gene was amplified using primers 341F (5′-CCTACGGGNGGCWGCAG-3′) and 785R (5′-GACTACHVGGGTATCTAATCC-3′) ( Klindworth et al., 2013 ). These primers provide broad bacterial coverage (~96%) with minimal bias ( Thijs et al., 2017 ) ( Fadeev et al., 2021 ). Each 50 μL PCR reaction comprised ~30 ng template DNA, 1× Taq buffer, 4 mM MgCl 2 , 0.2 mM dNTPs, 0.5 μM each primer, and 1 U Taq DNA polymerase. Cycling conditions: initial denaturation at 94°C for 3 min; 30 cycles of 94°C for 30 s, 56°C for 45 s, 72°C for 45 s; final extension at 72°C for 10 min. Amplicons were visualized on 1.5% agarose gel, purified using QIAquick PCR & Gel Cleanup Kit (QIAGEN, Germany), quantified with the PicoGreen dsDNA assay (Thermo Fisher Scientific), and then pooled equimolarly. Clean-up of pooled amplicons was conducted using AMPure XP beads (Beckman Coulter, USA). Library preparation & sequencing Library preparation followed standard Illumina MiSeq protocols ( Caporaso et al., 2012 ). Library size distributions were checked on an Agilent 2100 Bioanalyzer (Agilent Technologies, USA). Paired-end sequencing (2 × 250 bp) was performed at BGI (Shenzhen, China). Raw FASTQ data have been deposited in the NCBI Sequence Read Archive upon manuscript acceptance (accession to be added). Bioinformatic processing Demultiplexed paired-end FASTQ reads were processed using DADA2 (v1.30.0) in R (v4.3.2) ( Callahan et al., 2016 ). Forward and reverse reads were trimmed to remove adapters and low-quality bases; error rates were learned using learnErrors(), ASVs inferred with dada(), merged via mergePairs(), and chimeras removed with removeBimeraDenovo(). Taxonomic assignment was carried out against the Genome Taxonomy Database (GTDB release R207) ( Parks et al., 2022 ). The resulting ASV tables were used for downstream ecological and statistical analysis. Functional prediction Functional potential of ASVs was inferred using PICRUSt2 (v2.3.0-b) ( Douglas et al., 2020 ). Predicted gene families were mapped to KEGG Orthology (KO), Clusters of Orthologous Groups (COG), and MetaCyc pathways. Differential enrichment among plant hosts was assessed using Wilcoxon rank-sum and Kruskal–Wallis tests. Statistical & diversity analyses To account for sequencing depth variation, ASV tables were rarefied using the vegan package (v2.7-2) ( Oksanen et al., 2025 ) in R v4.3.2. Alpha-diversity metrics (Observed, Chao1, ACE, Shannon, Simpson, Good’s coverage) were calculated using phyloseq (v1.46.0) ( McMurdie & Holmes, 2013 ) and visualized with ggstatsplot (v0.12.1) ( Patil, 2021 ). Beta-diversity analyses used Bray–Curtis, unweighted and weighted UniFrac distances; ordinations (nMDS and PCoA) were generated via QIIME v1.8.0 ( Caporaso et al., 2012 ). For PCoA, 100 iterations of random subsampling (75% of the smallest library size) were used to ensure stability of ordination plots. Group differences were tested using PERMANOVA (p < 0.05). Dominant taxa at phylum and class levels were visualized using plot_bar in phyloseq. All statistical analyses were conducted in R v4.3.2 and figures were produced using ggplot2 ( Wickham, 2016 ). Results This study examined the endophytic bacterial communities of four desert plant species native to the Arabian Peninsula, namely Z. mandavillei (A), T. zeyheri (B), L. arabicum (C), and C. conglomeratus (D) ( Figure 1 ). These species are dominant components of the desert flora in the United Arab Emirates and exhibit exceptional tolerance to heat, salinity, and drought. Figure 1. Representative desert plant species were analyzed in this study. (A) Zygophyllum mandavillei , (B) Tribulus zeyheri Sond., (C) Limeum arabicum , and (D) Cyperus conglomeratus Rottb. These four native plants of the Arabian Peninsula were selected for microbiome profiling to explore their endophytic bacterial diversity and functional potential under arid conditions. Rarefaction curve A total of 110 root samples were analyzed, representing four plant species collected from five independent desert sites, with each site sample derived from a composite of 5 subsamples. Using 16S rRNA gene amplicon sequencing, we characterized the taxonomic composition, diversity, and predicted functional potential of their endospheric microbiomes. After quality control and removal of host-derived reads, a total of 3,660,664 high-quality sequences were obtained. Clustering at 97% similarity revealed 30 bacterial phyla, 15 classes, 20 orders, 27 families, and 21 genera. Rarefaction analysis indicated that sequencing depth was sufficient to capture the microbial diversity within each plant species ( Figure 2 ). The curves reached a plateau, confirming that read coverage adequately represented the bacterial communities associated with these samples. Figure 2. Rarefaction curves comparing species richness among desert plant microbiomes. Curves represent the relationship between sequencing depth and the number of observed amplicon sequence variants (ASVs) for each plant species. Alpha diversity of the studied endophytic bacterial communities To assess richness among the four desert plant species, alpha diversity was evaluated using six indices: Observed species, Chao1, ACE, Shannon, Simpson, and Good’s coverage ( Figure 3 ). All richness-related indices (Observed, Chao1, and ACE) showed significant differences among species (p < 0.05), with Z. mandavillei (A) exhibiting the highest richness, followed by L. arabicum (C) and C. conglomeratus (D), while T. zeyheri (B) displayed the lowest values. This indicates that Z. mandavillei supports a more diverse and taxonomically rich bacterial community than T. zeyheri. Figure 3. Alpha diversity analysis of endophytic bacterial communities across four desert plant species. Six diversity indices were applied to assess species richness and evenness: (3-A) Observed index (number of detected species), (3-B) Chao1 (estimated species richness), (3-C) ACE (community composition variability), (3-D) Shannon index (species richness and evenness), (3-E) Simpson index (dominance and evenness), and (3-F) Good’s coverage (sampling completeness). Diversity and evenness metrics (Shannon and Simpson) revealed distinct community structures across hosts. Shannon diversity was higher in Z. mandavillei (A), reflecting balanced taxa distribution, whereas T. zeyheri (B) showed low Shannon but high Simpson values, suggesting dominance by a few abundant taxa. Overall, each plant maintained a distinct endophytic bacterial diversity profile, with Z. mandavillei (A) harboring the richest and most even community, and T. zeyheri (B) showing reduced diversity, possibly due to host-specific selection or differing root microenvironments. Beta diversity of microbial communities Beta diversity analysis was performed to compare the overall microbial community composition among the four desert plant species. Three distance metrics were applied, including Bray–Curtis dissimilarity, weighted UniFrac, and unweighted UniFrac in order to capture both taxonomic and phylogenetic differences ( Figure 4 ). The Bray–Curtis dissimilarity index revealed a highly significant difference among the four groups (p = 0.001), indicating that each plant species harbors a distinct endophytic bacterial composition. This separation reflects strong host-specific effects on community assembly rather than random variation. Unweighted UniFrac analysis, which accounts for the presence or absence of taxa, supported these findings and emphasized that community composition differs substantially between hosts. The weighted UniFrac metric, which incorporates relative abundances, further indicated that compositional variation arises from both dominant and rare taxa, suggesting host-driven selection shaping the bacterial communities and demonstrating a pronounced dissimilarity in microbiome structure among the four desert plant species. Figure 4. Beta diversity analysis of microbial community composition among four desert plant species. The Bray–Curtis dissimilarity metric was used to assess compositional differences between samples, revealing distinct clustering patterns and high dissimilarity among the microbial communities associated with each plant species. Principal Coordinates Analysis (PCoA) of microbial community structure Principal Coordinates Analysis (PCoA) based on unweighted UniFrac distances was used to visualize compositional differences in endophytic bacterial communities among the four desert plant species ( Figure 5 ). The first two principal coordinates explained 36.51% and 11.28% of the total variance, respectively. The ordination plot revealed clear clustering by plant host (adonis R² = 0.30, p = 4 × 10 −4 ), confirming that community composition differs significantly among species. Z. mandavillei (A) and T. zeyheri (B) formed distinct, non-overlapping clusters, indicating highly specialized bacterial assemblages. In contrast, the microbiomes of L. arabicum (C) and C. conglomeratus (D) clustered closely together, suggesting they share a larger proportion of bacterial taxa and potentially similar ecological or physiological drivers of colonization. Taken together, these results point to a strong host effect in structuring the desert plant microbiome. While each species supports a characteristic bacterial consortium, the partial overlap between L. arabicum and C. conglomeratus implies that some microbial lineages may thrive across hosts with comparable root habitats or resource profiles. Figure 5. Principal Coordinates Analysis (PCoA) based on unweighted UniFrac distances. The analysis depicts phylogenetic beta diversity among microbial communities associated with the four desert plant species. Distinct clustering patterns indicate clear differences in community composition, reflecting variations in microbial structure and phylogenetic relationships across samples. Principal Coordinates Analysis (PCoA) based on weighted UniFrac distances To evaluate phylogenetic differences in the bacterial communities among the four desert plant species, a weighted UniFrac-based Principal Coordinates Analysis (PCoA) was conducted ( Figure 6 ). The first two axes explained 82.6% and 5.65% of the total variance, respectively, accounting for 88.25% of the variation in the dataset. Figure 6. Principal Coordinates Analysis (PCoA) based on weighted UniFrac distances. This analysis visualizes beta diversity among the microbial communities of the four desert plant species, incorporating both phylogenetic relationships and relative abundance of taxa. Distinct clustering patterns reflect compositional and abundance-based differences in microbial communities across samples. The ordination revealed a statistically significant separation among the plant-associated bacterial communities (adonis R² = 0.37; p = 0.0074), indicating that host identity strongly influences microbiome composition. Group A formed a well-defined cluster along PCoA axis 1, distinct from all other groups. Group B was positioned separately on the same axis, showing partial proximity to A but maintaining a unique composition. Groups C and D overlapped substantially, suggesting similarity in their endophytic bacterial communities; however, the slight displacement of D indicates minor but significant differences in community structure. These results demonstrate that host plant species play a major role in shaping bacterial community composition and phylogenetic structure, with Z. mandavillei (A) and T. zeyheri (B) harboring particularly distinct microbiomes, while L. arabicum and C. conglomeratus (C and D) share a more comparable microbial profile. Taxonomic composition of endophytic bacterial communities The microbial communities associated with the studied plant species displayed distinct taxonomic profiles across multiple taxonomic levels ( Figure 7 ). At the phylum level, all groups were dominated by Pseudomonadota, followed by Cyanobacteriota, Actinomycetota, and Gemmatimonadota. Pseudomonadota was consistently abundant in all plants, while Cyanobacteriota was particularly enriched in Z. mandavillei (A) and T. zeyheri (B). In contrast, Actinomycetota and Gemmatimonadota were more prevalent in L. arabicum (C) and C. conglomeratus (D), suggesting adaptation of these taxa to more nutrient-limited microhabitats. At the class level, Alphaproteobacteria dominated all four plants, confirming its central role as an endophytic lineage in desert ecosystems. Cyanophyceae was highly abundant in Z. mandavillei (A) and T. zeyheri (B) but nearly absent in L. arabicum (C) and C. conglomeratus (D). Gammaproteobacteria was enriched in Z. mandavillei (A), whereas Actinobacteria and Betaproteobacteria were markedly more abundant in L. arabicum (C) and C. conglomeratus (D), reflecting host-specific colonization preferences. Figure 7. Taxonomic composition of microbial communities across four desert plant species. The relative abundance of bacterial taxa is shown at multiple taxonomic levels: (A) class, (B) genus, (C) family, (D) phylum, and (E) species. The data illustrate distinct microbial community structures among the analyzed plants, highlighting dominant taxa contributing to functional and ecological diversity within the desert endosphere. At the family level, Methylobacteriaceae was among the most abundant families across all plant hosts, consistent with its known association with plant tissues. Z. mandavillei (A) exhibited additional enrichment of Oxalobacteraceae, Bacillaceae, Sphingomonadaceae, Erwiniaceae, and Caulobacteraceae. T. zeyheri (B) was dominated by Methylobacteriaceae, Roseobacteraceae, and Sphingomonadaceae. L. arabicum (C) and C. conglomeratus (D) showed high relative abundance of Methylobacteriaceae, Oxalobacteraceae, Bacillaceae, and Micrococcaceae, families commonly associated with stress tolerance and nutrient cycling. At the genus level, Microvirga, Massilia, and Domibacillus were enriched in Z. mandavillei (A), while Pseudarthrobacter dominated the communities of L. arabicum (C) and C. conglomeratus (D). T. zeyheri (B) exhibited lower overall diversity, with Methylobacterium and Sphingomonas as the main representatives. At the species level, Pseudarthrobacter phenanthrenivorans, Massilia consociata, Microvirga arabica, and Domibacillus epiphyticus were predominant in L. arabicum (C) and C. conglomeratus (D), indicating high similarity between their microbial communities. In contrast, Z. mandavillei (A) showed unique enrichment of Pantoea stewartii and Agrobacterium rubi, suggesting distinct host–microbe interactions and possibly specialized metabolic associations. Functional prediction and metabolic pathway analysis To assess the potential metabolic activity of the analyzed microbiota, predicted functional profiling of the endophytic bacterial communities was performed using PICRUSt2, and annotated using the MetaCyc, Clusters of Orthologous Groups (COG), and KEGG Orthology (KO) databases ( Figure 8 ). Figure 8. Predicted functional and metabolic pathway profiles of desert plant microbiomes. Functional annotations were performed using three databases to predict active metabolic pathways within the analyzed microbial communities: (8-A) MetaCyc pathways, (8-B) COG (Clusters of Orthologous Groups) functional categories, and (8-C) KO (KEGG Orthology) metabolic profiles. The results highlight key pathways associated with amino acid, carbohydrate, and lipid metabolism, as well as secondary metabolite biosynthesis and stress adaptation. At the MetaCyc level, pathways involved in the biosynthesis of amino acids, carbohydrates, fatty acids, and lipids were the most highly represented across all plant species. Pathways related to secondary metabolite and aromatic compound biosynthesis were also abundant, indicating strong metabolic potential for producing bioactive compounds. In contrast, pathways associated with carboxylate degradation, amino acid degradation, and inorganic nutrient metabolism occurred at moderate abundance, while antibiotic resistance and alcohol degradation were minimally represented. The COG annotation supported these results, showing enrichment in categories related to amino acid, carbohydrate, and lipid transport and metabolism, as well as secondary metabolite biosynthesis, transport, and catabolism. Other dominant functions included energy production and conversion, signal transduction, and defense mechanisms, reflecting the metabolic versatility and environmental responsiveness of the bacterial communities. The KEGG Orthology (KO) functional profiles further confirmed high representation of pathways involved in amino acid and carbohydrate metabolism, followed by xenobiotic biodegradation, terpenoid and polyketide metabolism, and DNA replication and repair. Functions linked to infectious or parasitic diseases, endocrine system, and neurodegenerative pathways appeared at low abundance, indicating that these endophytic communities are primarily oriented toward metabolic adaptation and biosynthesis rather than pathogenicity. These functional predictions suggest that the desert plant endophytes are metabolically active in nutrient cycling, secondary metabolite production, and environmental adaptation, supporting the resilience of their host plants under arid and nutrient-limited desert conditions. Discussion Current projections indicate that desertified land may expand to cover nearly 50% of terrestrial ecosystems by 2050, threatening biodiversity, food security, and soil fertility ( Bissenbayeva et al., 2024 ). A sustainable solution to confront this threat lies in the unique microbial community of the desert environment. These microbes demonstrate remarkable adaptability and stability under extreme abiotic stressors. Understanding their composition, functions, and metabolic patterns is essential to grasp their ecological role and potential contributions to climate adaptation and sustainable agriculture ( Alsharif et al., 2020 ). Recent studies have emphasized that desert microbiomes act as resilience models, providing insights into survival under aridity, salinity, and high temperature ( Milli et al., 2024 ; T. Zhang et al., 2022 ). Using an eDNA-based approach, this study characterized the endophytic microbial composition of four desert plants native to the Arabian Peninsula: Z. mandavillei, T. zeyheri, L. arabicum, and C. conglomeratus. Among them, L. arabicum and C. conglomeratus exhibited the highest microbial abundance and richness, while T. zeyheri showed the least diversity. To our knowledge, this is the first comparative microbial profiling of these four species, expanding the limited literature on desert endophytes of the Arabian Peninsula. Composition and functional diversity of the microbial community Our findings revealed that the most abundant bacterial classes across samples were Cyanophyceae, Alphaproteobacteria, Actinomycetia, and Gammaproteobacteria. These groups are commonly reported in arid soils and play critical roles in nutrient cycling, nitrogen fixation, and plant growth promotion ( Hood et al., 2017 ). Many of these taxa exhibit strong tolerance to UV radiation, salinity, and desiccation, traits essential for desert survival ( Nimbeshaho et al., 2024 ; Garcia-Pichel, 2023 ). Alphaproteobacteria and Actinomycetia include genera such as Streptomyces, Rhizobium, and Agrobacterium, previously documented for their ability to produce secondary metabolites and antibiotics under extreme stress ( Patel et al., 2024 ). The presence of Gemmatimonadota reflects its known role in phosphorus solubilization, improving nutrient-poor desert soils ( Craswell et al., 2021 ). The Actinomycetota class contributes to nitrogen and phosphorus mobilization by secreting extracellular enzymes that break down complex organic compounds, while also generating bioactive metabolites that inhibit pathogens, thus protecting desert seedlings ( Tidimalo et al., 2024 ). The dominance of Cyanophyceae highlights their dual role in carbon and nitrogen fixation and soil stabilization by producing extracellular polysaccharides that reduce erosion and enhance water retention ( Garcia-Pichel, 2023 ). Alphaproteobacteria further supports plant resilience by synthesizing phytohormones such as auxins and ACC deaminase that improve drought tolerance ( Fanai et al., 2024 ; Yu et al., 2025 ). Our data showed that Zygophyllum roots were enriched in Cyanophyceae and Proteobacteria, consistent with reports highlighting these taxa as dominant endosphere members in arid ecosystems ( Khan et al., 2022 ). Similarly, Tribulus was enriched in Cyanophyceae and Alphaproteobacteria, aligning with findings in T. terrestris that demonstrated phosphate solubilization and siderophore production as key adaptive mechanisms ( Eida et al., 2018 ). Metabolic pathways and functional resilience Functional predictions revealed highly active metabolic profiles characterized by strong biosynthetic and energy-generating pathways, consistent with prior studies ( Ronca et al., 2015 ). Enrichment of pathways involved in amino acid, lipid, and carbohydrate biosynthesis indicates that these microbes maintain strong primary metabolism even under nutrient scarcity. The dominance of post-translational modification, DNA replication, and transcription pathways reflects high metabolic plasticity and environmental resilience ( Guisbert et al., 2004 ). Lipid metabolism, particularly fatty acid biosynthesis, ensures membrane integrity and fluidity under heat stress and provides energy under nutrient limitation, enhancing microbial drought tolerance ( Coclet et al., 2022 ). Similarly, oxidative phosphorylation supports energy generation under fluctuating oxygen and moisture conditions. High carbohydrate metabolism underscores microbial ability to utilize complex carbon sources during scarcity, facilitating plant survival in nutrient-poor soils ( Y. Zhang et al., 2025 ). The elevated expression of amino acid and secondary metabolite pathways reflects the production of stress-protective compounds that contribute to plant–microbe mutualism ( Ortiz et al., 2021 ). Additionally, aromatic compound degradation supports carbon recycling by breaking down complex molecules such as lignin and phenols, thus promoting soil fertility ( Wang et al., 2025 ). Xenobiotic metabolism via cytochrome P450 further enables detoxification of harmful metabolites, safeguarding both plant and microbial communities ( Schütz et al., 2021 ). These findings underscore the metabolic adaptability of desert microbiomes, aligning with recent reports highlighting endophytic microbial resilience to extreme abiotic stress and their potential role in soil stabilization and greenhouse gas modulation ( Knight et al., 2024 ). Microbiomes, climate resilience, sustainability, and biotechnology Our study highlights the desert microbiome as a model for climate-resilient ecosystems, providing unique microbial solutions to address desertification challenges. These microbial consortia support sustainability through nutrient cycling, plant growth promotion, and carbon fixation ( Pointing & Belnap, 2012 ; Makhalanyane et al., 2015 ). Their adaptive traits, such as stress-protective pigments, osmolyte production, and efficient water retention, mirror the resilience mechanisms needed for future sustainable agriculture ( Bolan et al., 2024 ). Desert-adapted endophytes could be harnessed as bioinoculants or synthetic microbial communities to improve crop performance in degraded and arid lands. Recent reviews emphasize that inoculation with extremophilic microbes enhances soil fertility, reduces greenhouse gas emissions, and promotes drought tolerance in crops ( Soheili Esfahani, 2025 ; Ali et al., 2025 ). These microbial ecosystems could therefore contribute directly to climate change mitigation, supporting the United Nations Sustainable Development Goals for food security and environmental conservation. The unique endophytes identified here are candidates for isolating novel genes and metabolites with potential use in biostimulants, biofertilizers, and stress-tolerant crop engineering. Exploring their genomes and metabolites could also lead to drug discovery and environmental biotechnology innovations ( Pantigoso et al., 2025 ). Data citation Mousa et al. (2025) . Sequencing data for “Plant Microbiome of the Arabian Peninsula Desert Reveals Unique Structural and Functional Adaptations Supporting Climate Resilience.” NCBI Sequence Read Archive (SRA): BioSample SAMN52919711–SAMN52919714. Available at: https://www.ncbi.nlm.nih.gov/biosample/52919711 All sequencing data generated in this study have been deposited in the NCBI Sequence Read Archive (SRA) under accession numbers SAMN52919711, SAMN52919712, SAMN52919713, SAMN52919714. https://www.ncbi.nlm.nih.gov/biosample/52919711 https://www.ncbi.nlm.nih.gov/biosample/52919712 https://www.ncbi.nlm.nih.gov/biosample/52919713 https://www.ncbi.nlm.nih.gov/biosample/52919714 Data availability statement All sequencing data generated in this study have been deposited in the NCBI Sequence Read Archive (SRA) under BioSample accession numbers SAMN52919711, SAMN52919712, SAMN52919713, and SAMN52919714. The data can be accessed at: https://www.ncbi.nlm.nih.gov/biosample/52919711 https://www.ncbi.nlm.nih.gov/biosample/52919712 https://www.ncbi.nlm.nih.gov/biosample/52919713 https://www.ncbi.nlm.nih.gov/biosample/52919714 References Abdullah MT: Conserving the biodiversity of Kuwait through DNA barcoding the flora.2017. 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Publisher Full Text Comments on this article Comments (0) Version 1 VERSION 1 PUBLISHED 06 Jan 2026 ADD YOUR COMMENT Comment Author details Author details 1 Al Ain University College of Pharmacy, Al Ain, Abu Dhabi, United Arab Emirates 2 Department of Pharmacognosy, Faculty of Pharmacy, Mansoura University, Dakahlia Governorate, Egypt Walaa K. Mousa Roles: Conceptualization, Formal Analysis, Funding Acquisition, Methodology, Resources, Supervision, Writing – Review & Editing Ruqaia AlShami Roles: Formal Analysis, Methodology, Writing – Original Draft Preparation Rose Ghemrawi Roles: Formal Analysis, Writing – Review & Editing Competing interests No competing interests were disclosed. Grant information The research is supported by an external grant from Sandooq Al Watan organization, UAE to the PI, WKM. Project ID: PRJ-SWARD-711. Grant NO: SWARD-F23-020. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Article Versions (1) version 1 Published: 06 Jan 2026, 15:9 https://doi.org/10.12688/f1000research.172949.1 Copyright © 2026 Mousa WK et al . This is an open access article distributed under the terms of the Creative Commons Attribution License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Download Export To Sciwheel Bibtex EndNote ProCite Ref. Manager (RIS) Sente metrics Views Downloads F1000Research - - PubMed Central info_outline Data from PMC are received and updated monthly. - - Citations open_in_new 0 open_in_new 0 open_in_new SEE MORE DETAILS CITE how to cite this article Mousa WK, AlShami R and Ghemrawi R. Plant Microbiome of the Arabian Peninsula Desert Reveals Unique Structural and Functional Adaptations Supporting Climate Resilience [version 1; peer review: 1 approved with reservations] . F1000Research 2026, 15 :9 ( https://doi.org/10.12688/f1000research.172949.1 ) NOTE: If applicable, it is important to ensure the information in square brackets after the title is included in all citations of this article. COPY CITATION DETAILS track receive updates on this article Track an article to receive email alerts on any updates to this article. TRACK THIS ARTICLE Share Open Peer Review Current Reviewer Status: ? Key to Reviewer Statuses VIEW HIDE Approved The paper is scientifically sound in its current form and only minor, if any, improvements are suggested Approved with reservations A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit. Not approved Fundamental flaws in the paper seriously undermine the findings and conclusions Version 1 VERSION 1 PUBLISHED 06 Jan 2026 Views 0 Cite How to cite this report: liu b and Wu Y. Reviewer Report For: Plant Microbiome of the Arabian Peninsula Desert Reveals Unique Structural and Functional Adaptations Supporting Climate Resilience [version 1; peer review: 1 approved with reservations] . F1000Research 2026, 15 :9 ( https://doi.org/10.5256/f1000research.190719.r448372 ) The direct URL for this report is: https://f1000research.com/articles/15-9/v1#referee-response-448372 NOTE: it is important to ensure the information in square brackets after the title is included in this citation. Close Copy Citation Details Reviewer Report 03 Feb 2026 bao liu , Genetics, Northeast Normal University, Changchun, China Ying Wu , Key Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, China Approved with Reservations VIEWS 0 https://doi.org/10.5256/f1000research.190719.r448372 This manuscript presents an amplicon-based characterization of root endophytic bacterial communities associated with four desert-adapted plant species sampled from the Al-Ain desert region (UAE). Based on 16S rRNA V3-V4 sequencing, the authors compared community composition and diversity across hosts and ... Continue reading READ ALL This manuscript presents an amplicon-based characterization of root endophytic bacterial communities associated with four desert-adapted plant species sampled from the Al-Ain desert region (UAE). Based on 16S rRNA V3-V4 sequencing, the authors compared community composition and diversity across hosts and used PICRUSt2 to infer potential functions, thereby offering useful baseline insights into endophyte assemblages in a relatively under-studied arid plant system. The overall approach is appropriate and employs commonly accepted methods. The deposition of sequencing data supports open and independent interrogations to ensure reproducible research. However, several clarifications are needed and hopefully to further strengthen interpretability and readability. Specific comments are listed below. Major comments 1. The manuscript should reconcile and clearly enumerate sample numbers and the compositing scheme, as different parts of the text used different sample counts and terminology, which currently makes it difficult to understand how many independent biological units were ultimately sequenced and statistically analyzed. 2. Please clarify whether the four host species were sampled in close spatial proximity and under comparable soil/microhabitat conditions, because the observed between-host community differences could reflect both host specificity and spatial/soil heterogeneity; if these effects cannot be separated, this should be acknowledged explicitly as a limitation and the language around host-driven differences should be tempered accordingly. 3. Several results are described at species level, but 16S V3-V4 amplicons often cannot reliably resolve bacterial taxa down to species across many groups (Janda & Abbott, 2007; Johnson et al., 2019). Please ensure that species-level labels are only used when classification confidence supports them, otherwise interpret and discuss findings primarily at genus (or higher) taxon levels might be more appropriate. 4. PICRUSt2 results should be consistently framed as predicted/inferred functional potential rather than demonstrated function; statements linking specific pathways to stress tolerance would benefit from more cautious wording and a brief discussion of how key functional hypotheses could be validated in future work (e.g., metagenomics, isolate-based assays, or host phenotype associations). 5. Because all four hosts are drought-tolerant xerophytes, the paper would be more informative if it also include a brief “shared/core” perspective in addition to contrasts among hosts, for example highlighting taxa (and predicted functional features) consistently present across all hosts that might plausibly relate to drought resilience. Minor comments 1. Please standardize and define terminology for “plant samples”, “root samples”, “composite samples”, and “pooled subsamples” to improve readability and avoid ambiguity. 2. Please ensure that key analysis parameters needed for replication are fully reported (e.g., rarefaction depth if applied, exact distance metrics used for ordinations, and the PERMANOVA specification). 3. Consider rephrasing terms like “genomic overview” to avoid implying whole-genome or metagenomic sequencing, since the study is based on 16S amplicon profiling with functional inference. Is the work clearly and accurately presented and does it cite the current literature? Yes Is the study design appropriate and is the work technically sound? Yes Are sufficient details of methods and analysis provided to allow replication by others? Partly If applicable, is the statistical analysis and its interpretation appropriate? Yes Are all the source data underlying the results available to ensure full reproducibility? Yes Are the conclusions drawn adequately supported by the results? Partly References 1. Janda J, Abbott S: 16S rRNA Gene Sequencing for Bacterial Identification in the Diagnostic Laboratory: Pluses, Perils, and Pitfalls. Journal of Clinical Microbiology . 2007; 45 (9): 2761-2764 Publisher Full Text 2. Johnson J, Spakowicz D, Hong B, Petersen L, et al.: Evaluation of 16S rRNA gene sequencing for species and strain-level microbiome analysis. Nature Communications . 2019; 10 (1). Publisher Full Text Competing Interests: No competing interests were disclosed. Reviewer Expertise: Review author(s): Ying Wu, Bao Liu Affiliation (for both authors): Key Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun 130024, China Area(s) of research/expertise: Plant polyploid genome evolution; Plant epigenetics; Plant-microbe interactions. We confirm that we have read this submission and believe that we have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however we have significant reservations, as outlined above. Close READ LESS CITE CITE HOW TO CITE THIS REPORT liu b and Wu Y. Reviewer Report For: Plant Microbiome of the Arabian Peninsula Desert Reveals Unique Structural and Functional Adaptations Supporting Climate Resilience [version 1; peer review: 1 approved with reservations] . F1000Research 2026, 15 :9 ( https://doi.org/10.5256/f1000research.190719.r448372 ) The direct URL for this report is: https://f1000research.com/articles/15-9/v1#referee-response-448372 NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article. COPY CITATION DETAILS Report a concern Respond or Comment COMMENT ON THIS REPORT Comments on this article Comments (0) Version 1 VERSION 1 PUBLISHED 06 Jan 2026 ADD YOUR COMMENT Comment keyboard_arrow_left keyboard_arrow_right Open Peer Review Reviewer Status info_outline Alongside their report, reviewers assign a status to the article: Approved The paper is scientifically sound in its current form and only minor, if any, improvements are suggested Approved with reservations A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit. Not approved Fundamental flaws in the paper seriously undermine the findings and conclusions Reviewer Reports Invited Reviewers 1 Version 1 06 Jan 26 read bao liu , Northeast Normal University, Changchun, China Ying Wu , Northeast Normal University, Changchun, China Comments on this article All Comments (0) Add a comment Sign up for content alerts Sign Up You are now signed up to receive this alert Browse by related subjects keyboard_arrow_left Back to all reports Reviewer Report 0 Views copyright © 2026 liu b et al. This is an open access peer review report distributed under the terms of the Creative Commons Attribution License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 03 Feb 2026 | for Version 1 bao liu , Genetics, Northeast Normal University, Changchun, China Ying Wu , Key Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun, China 0 Views copyright © 2026 liu b et al. This is an open access peer review report distributed under the terms of the Creative Commons Attribution License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. format_quote Cite this report speaker_notes Responses (0) Approved With Reservations info_outline Alongside their report, reviewers assign a status to the article: Approved The paper is scientifically sound in its current form and only minor, if any, improvements are suggested Approved with reservations A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit. Not approved Fundamental flaws in the paper seriously undermine the findings and conclusions This manuscript presents an amplicon-based characterization of root endophytic bacterial communities associated with four desert-adapted plant species sampled from the Al-Ain desert region (UAE). Based on 16S rRNA V3-V4 sequencing, the authors compared community composition and diversity across hosts and used PICRUSt2 to infer potential functions, thereby offering useful baseline insights into endophyte assemblages in a relatively under-studied arid plant system. The overall approach is appropriate and employs commonly accepted methods. The deposition of sequencing data supports open and independent interrogations to ensure reproducible research. However, several clarifications are needed and hopefully to further strengthen interpretability and readability. Specific comments are listed below. Major comments 1. The manuscript should reconcile and clearly enumerate sample numbers and the compositing scheme, as different parts of the text used different sample counts and terminology, which currently makes it difficult to understand how many independent biological units were ultimately sequenced and statistically analyzed. 2. Please clarify whether the four host species were sampled in close spatial proximity and under comparable soil/microhabitat conditions, because the observed between-host community differences could reflect both host specificity and spatial/soil heterogeneity; if these effects cannot be separated, this should be acknowledged explicitly as a limitation and the language around host-driven differences should be tempered accordingly. 3. Several results are described at species level, but 16S V3-V4 amplicons often cannot reliably resolve bacterial taxa down to species across many groups (Janda & Abbott, 2007; Johnson et al., 2019). Please ensure that species-level labels are only used when classification confidence supports them, otherwise interpret and discuss findings primarily at genus (or higher) taxon levels might be more appropriate. 4. PICRUSt2 results should be consistently framed as predicted/inferred functional potential rather than demonstrated function; statements linking specific pathways to stress tolerance would benefit from more cautious wording and a brief discussion of how key functional hypotheses could be validated in future work (e.g., metagenomics, isolate-based assays, or host phenotype associations). 5. Because all four hosts are drought-tolerant xerophytes, the paper would be more informative if it also include a brief “shared/core” perspective in addition to contrasts among hosts, for example highlighting taxa (and predicted functional features) consistently present across all hosts that might plausibly relate to drought resilience. Minor comments 1. Please standardize and define terminology for “plant samples”, “root samples”, “composite samples”, and “pooled subsamples” to improve readability and avoid ambiguity. 2. Please ensure that key analysis parameters needed for replication are fully reported (e.g., rarefaction depth if applied, exact distance metrics used for ordinations, and the PERMANOVA specification). 3. Consider rephrasing terms like “genomic overview” to avoid implying whole-genome or metagenomic sequencing, since the study is based on 16S amplicon profiling with functional inference. Is the work clearly and accurately presented and does it cite the current literature? Yes Is the study design appropriate and is the work technically sound? Yes Are sufficient details of methods and analysis provided to allow replication by others? Partly If applicable, is the statistical analysis and its interpretation appropriate? Yes Are all the source data underlying the results available to ensure full reproducibility? Yes Are the conclusions drawn adequately supported by the results? Partly References 1. Janda J, Abbott S: 16S rRNA Gene Sequencing for Bacterial Identification in the Diagnostic Laboratory: Pluses, Perils, and Pitfalls. Journal of Clinical Microbiology . 2007; 45 (9): 2761-2764 Publisher Full Text 2. Johnson J, Spakowicz D, Hong B, Petersen L, et al.: Evaluation of 16S rRNA gene sequencing for species and strain-level microbiome analysis. Nature Communications . 2019; 10 (1). Publisher Full Text Competing Interests No competing interests were disclosed. Reviewer Expertise Review author(s): Ying Wu, Bao Liu Affiliation (for both authors): Key Laboratory of Molecular Epigenetics of the Ministry of Education (MOE), Northeast Normal University, Changchun 130024, China Area(s) of research/expertise: Plant polyploid genome evolution; Plant epigenetics; Plant-microbe interactions. We confirm that we have read this submission and believe that we have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however we have significant reservations, as outlined above. reply Respond to this report Responses (0) liu b and Wu Y. Peer Review Report For: Plant Microbiome of the Arabian Peninsula Desert Reveals Unique Structural and Functional Adaptations Supporting Climate Resilience [version 1; peer review: 1 approved with reservations] . F1000Research 2026, 15 :9 ( https://doi.org/10.5256/f1000research.190719.r448372) NOTE: it is important to ensure the information in square brackets after the title is included in this citation. The direct URL for this report is: https://f1000research.com/articles/15-9/v1#referee-response-448372 Alongside their report, reviewers assign a status to the article: Approved - the paper is scientifically sound in its current form and only minor, if any, improvements are suggested Approved with reservations - A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit. Not approved - fundamental flaws in the paper seriously undermine the findings and conclusions Adjust parameters to alter display View on desktop for interactive features Includes Interactive Elements View on desktop for interactive features Competing Interests Policy Provide sufficient details of any financial or non-financial competing interests to enable users to assess whether your comments might lead a reasonable person to question your impartiality. 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