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      Defining the root endosphere and rhizosphere microbiomes from the World Olive Germplasm Collection

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          Abstract

          The bacterial and fungal communities from the olive ( Olea europaea L.) root systems have not yet been simultaneously studied. We show in this work that microbial communities from the olive root endosphere are less diverse than those from the rhizosphere. But more relevant was to unveil that olive belowground communities are mainly shaped by the genotype of the cultivar when growing under the same environmental, pedological and agronomic conditions. Furthermore, Actinophytocola, Streptomyces and Pseudonocardia are the most abundant bacterial genera in the olive root endosphere, Actinophytocola being the most prevalent genus by far. In contrast, Gp6, Gp4, Rhizobium and Sphingomonas are the main genera in the olive rhizosphere. Canalisporium, Aspergillus, Minimelanolocus and Macrophomina are the main fungal genera present in the olive root system. Interestingly enough, a large number of as yet unclassified fungal sequences (class level) were detected in the rhizosphere. From the belowground microbial profiles here reported, it can be concluded that the genus Actinophytocola may play an important role in olive adaptation to environmental stresses. Moreover, the huge unknown fungal diversity here uncovered suggests that fungi with important ecological function and biotechnological potential are yet to be identified.

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          Improved software detection and extraction of ITS1 and ITS2 from ribosomal ITS sequences of fungi and other eukaryotes for analysis of environmental sequencing data

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            Plant compartment and biogeography affect microbiome composition in cultivated and native Agave species

            Summary Desert plants are hypothesized to survive the environmental stress inherent to these regions in part thanks to symbioses with microorganisms, and yet these microbial species, the communities they form, and the forces that influence them are poorly understood. Here we report the first comprehensive investigation of the microbial communities associated with species of Agave, which are native to semiarid and arid regions of Central and North America and are emerging as biofuel feedstocks. We examined prokaryotic and fungal communities in the rhizosphere, phyllosphere, leaf and root endosphere, as well as proximal and distal soil samples from cultivated and native agaves, through Illumina amplicon sequencing. Phylogenetic profiling revealed that the composition of prokaryotic communities was primarily determined by the plant compartment, whereas the composition of fungal communities was mainly influenced by the biogeography of the host species. Cultivated A. tequilana exhibited lower levels of prokaryotic diversity compared with native agaves, although no differences in microbial diversity were found in the endosphere. Agaves shared core prokaryotic and fungal taxa known to promote plant growth and confer tolerance to abiotic stress, which suggests common principles underpinning Agave–microbe interactions.
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              Aerobic proteobacterial methylotrophs in Movile Cave: genomic and metagenomic analyses

              Background Movile Cave (Mangalia, Romania) is a unique ecosystem where the food web is sustained by microbial primary production, analogous to deep-sea hydrothermal vents. Specifically, chemoautotrophic microbes deriving energy from the oxidation of hydrogen sulphide and methane form the basis of the food web. Results Here, we report the isolation of the first methane-oxidizing bacterium from the Movile Cave ecosystem, Candidatus Methylomonas sp. LWB, a new species and representative of Movile Cave microbial mat samples. While previous research has suggested a prevalence of anoxic conditions in deeper lake water and sediment, using small-scale shotgun metagenome sequencing, we show that metabolic genes encoding enzymes for aerobic methylotrophy are prevalent in sediment metagenomes possibly indicating the presence of microoxic conditions. Moreover, this study also indicates that members within the family Gallionellaceae (Sideroxydans and Gallionella) were the dominant taxa within the sediment microbial community, thus suggesting a major role for microaerophilic iron-oxidising bacteria in nutrient cycling within the Movile Cave sediments. Conclusions In this study, based on phylogenetic and metabolic gene surveys of metagenome sequences, the possibility of aerobic microbial processes (i.e., methylotrophy and iron oxidation) within the sediment is indicated. We also highlight significant gaps in our knowledge on biogeochemical cycles within the Movile Cave ecosystem, and the need to further investigate potential feedback mechanisms between microbial communities in both lake sediment and lake water. Electronic supplementary material The online version of this article (10.1186/s40168-017-0383-2) contains supplementary material, which is available to authorized users.
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                Author and article information

                Contributors
                manuel.fernandez@eez.csic.es
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                31 December 2019
                31 December 2019
                2019
                : 9
                : 20423
                Affiliations
                [1 ]ISNI 0000 0001 2183 4846, GRID grid.4711.3, Departamento de Microbiología del Suelo y Sistemas Simbióticos, Estación Experimental del Zaidín, , Consejo Superior de Investigaciones Científicas (CSIC), ; Calle Profesor Albareda 1, 18008 Granada, Spain
                [2 ]GRID grid.473633.6, Departamento de Protección de Cultivos, , Instituto de Agricultura Sostenible, CSIC. Campus ‘Alameda del Obispo’ s/n, ; Avd. Menéndez Pidal s/n, 14004 Córdoba, Spain
                [3 ]ISNI 0000 0001 2195 4653, GRID grid.425162.6, Área Mejora y Biotecnología, , IFAPA-Centro Alameda del Obispo, ; Avda. Menéndez Pidal s/n, 14080 Córdoba, Spain
                Author information
                http://orcid.org/0000-0002-8781-8133
                http://orcid.org/0000-0003-1895-5895
                http://orcid.org/0000-0003-2366-6908
                Article
                56977
                10.1038/s41598-019-56977-9
                6938483
                31892747
                cf020861-acae-46ea-841d-e3fe376efb6a
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 20 March 2019
                : 19 December 2019
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                © The Author(s) 2019

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                microbiome,agroecology
                Uncategorized
                microbiome, agroecology

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