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      Endophytic bacterial diversity in the phyllosphere of Amazon Paullinia cupana associated with asymptomatic and symptomatic anthracnose

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          Abstract

          Endophytes colonize an ecological niche similar to that of phytopathogens, which make them candidate for disease suppression. Anthracnose is a disease caused by Colletotrichum spp., a phytopathogen that can infect guarana ( Paullinia cupana), an important commercial crop in the Brazilian Amazon. We investigated the diversity of endophytic bacteria inhabiting the phyllosphere of asymptomatic and symptomatic anthracnose guarana plants. The PCR-denaturation gradient gel electrophoresis (PCR-DGGE) fingerprints revealed differences in the structure of the evaluated communities. Detailed analysis of endophytic bacteria composition using culture-dependent and 16S rRNA clone libraries revealed the presence of Firmicutes, Proteobacteria, Actinobacteria, Bacteroidetes, and Acidobacteria phyla . Firmicutes comprised the majority of isolates in asymptomatic plants (2.40E −4). However, cloning and sequencing of 16S rRNA revealed differences at the genus level for Neisseria (1.4E −4), Haemophilus (2.1E −3) and Arsenophonus (3.6E −5) in asymptomatic plants, Aquicella (3.5E −3) in symptomatic anthracnose plants, and Pseudomonas (1.1E −3), which was mainly identified in asymptomatic plants. In cross-comparisons of the endophytic bacterial communities as a whole, symptomatic anthracnose plants contained higher diversity, as reflected in the Shannon–Weaver and Simpson indices estimation ( P < 0.05). Similarly, comparisons using LIBSHUFF and heatmap analysis for the relative abundance of operational taxonomic units (OTUs) showed differences between endophytic bacterial communities. These data are in agreement with the NMSD and ANOSIM analysis of DGGE profiles. Our results suggest that anthracnose can restructure endophytic bacterial communities by selecting certain strains in the phyllosphere of P. cupana. The understanding of these interactions is important for the development of strategies of biocontrol for Colletotrichum.

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          The online version of this article (doi:10.1186/s40064-015-1037-0) contains supplementary material, which is available to authorized users.

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          Statistical design and analysis for a 'biological effects' study

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            Bacterial Communities Associated with the Leaves and the Roots of Arabidopsis thaliana

            Diverse communities of bacteria inhabit plant leaves and roots and those bacteria play a crucial role for plant health and growth. Arabidopsis thaliana is an important model to study plant pathogen interactions, but little is known about its associated bacterial community under natural conditions. We used 454 pyrosequencing to characterize the bacterial communities associated with the roots and the leaves of wild A. thaliana collected at 4 sites; we further compared communities on the outside of the plants with communities in the endophytic compartments. We found that the most heavily sequenced bacteria in A. thaliana associated community are related to culturable species. Proteobacteria, Actinobacteria, and Bacteroidetes are the most abundant phyla in both leaf and root samples. At the genus level, sequences of Massilia and Flavobacterium are prevalent in both samples. Organ (leaf vs root) and habitat (epiphytes vs endophytes) structure the community. In the roots, richness is higher in the epiphytic communities compared to the endophytic compartment (P = 0.024), while the reverse is true for the leaves (P = 0.032). Interestingly, leaf and root endophytic compartments do not differ in richness, diversity and evenness, while they differ in community composition (P = 0.001). The results show that although the communities associated with leaves and roots share many bacterial species, the associated communities differ in structure.
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              The Diversity of Archaea and Bacteria in Association with the Roots of Zea mays L.

              The diversity of bacteria and archaea associating on the surface and interior of maize roots (Zea mays L.) was investigated. A bacterial 16S rDNA primer was designed to amplify bacterial sequences directly from maize roots by PCR to the exclusion of eukaryotic and chloroplast DNA. The mitochondrial sequence from maize was easily separated from the PCR-amplified bacterial sequences by size fractionation. The culturable component of the bacterial community was also assessed, reflecting a community composition different from that of the clone library. The phylogenetic overlap between organisms obtained by cultivation and those identified by direct PCR amplification of 16S rDNA was 48%. Only 4 bacterial divisions were found in the culture collection, which represented 27 phylotypes, whereas 6 divisions were identified in the clonal analysis, comprising 74 phylotypes, including a member of the OP10 candidate division originally described as a novel division level lineage in a Yellowstone hot spring. The predominant group in the culture collection was the actinobacteria and within the clone library, the a-proteobacteria predominated. The population of maize-associated proteobacteria resembled the proteobacterial population of a typical soil community within which resided a subset of specific plant-associated bacteria, such as Rhizobium- and Herbaspirillum-related phylotypes. The representation of phylotypes within other divisions (OP10 and Acidobacterium) suggests that maize roots support a distinct bacterial community. The diversity within the archaeal domain was low. Of the 50 clones screened, 6 unique sequence types were identified, and 5 of these were highly related to each other (sharing 98% sequence identity). The archaeal sequences clustered with good bootstrap support near Marine group I (crenarchaea) and with Marine group II (euryarchaea) uncultured archaea. The results suggest that maize supports a diverse root-associated microbial community composed of species that for the first time have been described as inhabitants of a plant-root environment.
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                Author and article information

                Contributors
                andreabogas@hotmail.com
                almirjferreira@usp.br
                wlaraujo@usp.br
                spartaco.biotec@gmail.com
                ewkitaji@usp.br
                ptlacava@ufscar.br
                jlazevedo@usp.br
                Journal
                Springerplus
                Springerplus
                SpringerPlus
                Springer International Publishing (Cham )
                2193-1801
                13 June 2015
                13 June 2015
                2015
                : 4
                : 258
                Affiliations
                [ ]Department of Genetics, “Luiz de Queiroz” College of Agriculture, University of São Paulo, Av. Pádua Dias 11, PO BOX 83, Piracicaba, SP 13400-970 Brazil
                [ ]Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, 1374-Ed. Biomédicas II, Cidade Universitária, São Paulo, SP 05508-900 Brazil
                [ ]Molecular Diagnostic Laboratory, Biotechnology Division, Federal University of Amazon, Av. Gal. Rodrigo Octávio Jordão, 3000, Manaus, AM 69.077-000 Brazil
                [ ]Department of Plant Pathology and Nematology, ‘‘Luiz de Queiroz’’ College of Agriculture, University of São Paulo, Av. Pádua Dias 11, Piracicaba, SP 13418-900 Brazil
                [ ]Center of Biological Sciences and Health, Federal University of São Carlos, Via Washington Luís km 235, PO BOX 676, São Carlos, SP 13565-905 Brazil
                Article
                1037
                10.1186/s40064-015-1037-0
                4467821
                26090305
                0438c150-e6ac-410f-8b7f-9cc660b80222
                © Bogas et al. 2015

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.

                History
                : 8 April 2015
                : 13 May 2015
                Categories
                Research
                Custom metadata
                © The Author(s) 2015

                Uncategorized
                colletotrichum,culture dependent,endophytes,pcr-dgge,clone library,microbial diversity
                Uncategorized
                colletotrichum, culture dependent, endophytes, pcr-dgge, clone library, microbial diversity

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