<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wu S</submitter><funding>the Science and Technology Program of Guizhou Province</funding><funding>the Talent Fund of Guizhou University</funding><funding>the National Natural Science Foundation of China</funding><pagination>33</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12911403</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Karst rocky desertification poses a serious threat to the ecosystems of southwest China, where Hypnum leptothallum plays a crucial role in forming microbial crusts essential for restoration. However, the use of native microbial applications in this area remains largely unexplored.&lt;h4>Results&lt;/h4>In this study, the host-associated microbial communities of H. leptothallum from four severely desertified regions in Guizhou Province were characterized using high-throughput sequencing. The results revealed conserved α- and β-diversity, with dominant bacterial phyla being Pseudomonadota (34-47%) and Actinomycetota (23-35%), and fungal phyla being Ascomycota (57-83%) and Basidiomycota (14-32%). Subsequent carbon-source preference analysis guided the formulation of specialized media (e.g., α-D-lactose, N-acetyl-D-glucosamine) to isolate culturable strains, with cross-referencing identifying 14 bacterial and 36 fungal species consistently shared between sequencing and cultivation. Functional evaluation demonstrated bacterial dominance in inorganic phosphorus solubilization (68% of strains), protease synthesis (76%), ammonia production (56%), and indole-3-acetic acid biosynthesis (62%), while fungi excelled in organophosphorus solubilization. Further drought tolerance and gametophyte co-culture assays identified 10 drought-resistant bacterial strains and 16 strains significantly enhancing H. leptothallum growth within 7 days.&lt;h4>Conclusions&lt;/h4>These functionally validated strains, particularly drought-adapted and growth-stimulating species closely related to Rhodococcus erythropolis, provide targeted microbial resources for developing synthetic inoculants to optimize artificial crust propagation in karst restoration.</pubmed_abstract><journal>Environmental microbiome</journal><pubmed_title>Exploring the diversity and potential of host-associated microorganisms in Hypnum leptothallum to enhance plant resilience to drought stress for karst desertification restoration.</pubmed_title><pmcid>PMC12911403</pmcid><funding_grant_id>32060038</funding_grant_id><funding_grant_id>[2020]9</funding_grant_id><funding_grant_id>32160026</funding_grant_id><funding_grant_id>QianKeHe-ZK[2022]034</funding_grant_id><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>He Z</pubmed_authors><pubmed_authors>Cao W</pubmed_authors><pubmed_authors>Lu Y</pubmed_authors><pubmed_authors>Wu S</pubmed_authors><pubmed_authors>Qu J</pubmed_authors><pubmed_authors>Xiang Y</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Zuo Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exploring the diversity and potential of host-associated microorganisms in Hypnum leptothallum to enhance plant resilience to drought stress for karst desertification restoration.</name><description>&lt;h4>Background&lt;/h4>Karst rocky desertification poses a serious threat to the ecosystems of southwest China, where Hypnum leptothallum plays a crucial role in forming microbial crusts essential for restoration. However, the use of native microbial applications in this area remains largely unexplored.&lt;h4>Results&lt;/h4>In this study, the host-associated microbial communities of H. leptothallum from four severely desertified regions in Guizhou Province were characterized using high-throughput sequencing. The results revealed conserved α- and β-diversity, with dominant bacterial phyla being Pseudomonadota (34-47%) and Actinomycetota (23-35%), and fungal phyla being Ascomycota (57-83%) and Basidiomycota (14-32%). Subsequent carbon-source preference analysis guided the formulation of specialized media (e.g., α-D-lactose, N-acetyl-D-glucosamine) to isolate culturable strains, with cross-referencing identifying 14 bacterial and 36 fungal species consistently shared between sequencing and cultivation. Functional evaluation demonstrated bacterial dominance in inorganic phosphorus solubilization (68% of strains), protease synthesis (76%), ammonia production (56%), and indole-3-acetic acid biosynthesis (62%), while fungi excelled in organophosphorus solubilization. Further drought tolerance and gametophyte co-culture assays identified 10 drought-resistant bacterial strains and 16 strains significantly enhancing H. leptothallum growth within 7 days.&lt;h4>Conclusions&lt;/h4>These functionally validated strains, particularly drought-adapted and growth-stimulating species closely related to Rhodococcus erythropolis, provide targeted microbial resources for developing synthetic inoculants to optimize artificial crust propagation in karst restoration.</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-09T13:12:50.759Z</modification><creation>2026-07-09T13:09:56.015Z</creation></dates><accession>S-EPMC12911403</accession><cross_references><pubmed>41580881</pubmed><doi>10.1186/s40793-026-00849-z</doi></cross_references></HashMap>