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Bacterial soil community in a Brazilian sugarcane field
Authors:Francisco Dini-Andreote  Fernando Dini Andreote  Rodrigo Costa  Rodrigo Gouvêa Taketani  Jan Dirk van Elsas  Welington Luiz Araújo
Affiliation:1. Department of Genetics, Escola Superior de Agricultura “Luiz de Queiroz”, University of S?o Paulo, Piracicaba, SP, Brazil
5. Department of Microbial Ecology, Centre for Ecological and Evolutionary Studies (CEES), University of Groningen (RUG), Kerklaan 30, Groningen, 9751 NN, The Netherlands
2. Department of Soil Science, Escola Superior de Agricultura “Luiz de Queiroz”, University of S?o Paulo, Piracicaba, SP, Brazil
3. Microbial Ecology and Evolution Research Group, Centre of Marine Sciences (CCMAR-CIMAR), University of Algarve, Gambelas, 8005-139, Faro, Portugal
4. Centro de Energia Nuclear na Agricultura, Universidade de S?o Paulo, Piracicaba, SP, Brazil
6. Center of Biotechnological Researches, University of Mogi das Cruzes, Mogi das Cruzes, SP, Brazil
7. Laboratory of Molecular Biology and Microbial Ecology, NIB, University of Mogi das Cruzes, 08780-911, Mogi das Cruzes, SP, Brazil
Abstract:The assessment of bacterial communities in soil gives insight into microbial behavior under prevailing environmental conditions. In this context, we assessed the composition of soil bacterial communities in a Brazilian sugarcane experimental field. The experimental design encompassed plots containing common sugarcane (variety SP80-1842) and its transgenic form (IMI-1 — imazapyr herbicide resistant). Plants were grown in such field plots in a completely randomized design with three treatments, which addressed the factors transgene and imazapyr herbicide application. Soil samples were taken at three developmental stages during plant growth and analyzed using 16S ribosomal RNA (rRNA)-based PCR-denaturing gradient gel electrophoresis (PCR-DGGE) and clone libraries. PCR-DGGE fingerprints obtained for the total bacterial community and specific bacterial groups — Actinobacteria, Alphaproteobacteria and Betaproteobacteria — revealed that the structure of these assemblages did not differ over time and among treatments. Nevertheless, slight differences among 16S rRNA gene clone libraries constructed from each treatment could be observed at particular cut-off levels. Altogether, the libraries encompassed a total of eleven bacterial phyla and the candidate divisions TM7 and OP10. Clone sequences affiliated with the Proteobacteria, Actinobacteria, Firmicutes and Acidobacteria were, in this order, most abundant. Accurate phylogenetic analyses were performed for the phyla Acidobacteria and Verrucomicrobia, revealing the structures of these groups, which are still poorly understood as to their importance for soil functioning and sustainability under agricultural practices.
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