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      In vivo function and comparative genomic analyses of the Drosophila gut microbiota identify candidate symbiosis factors

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          Abstract

          Symbiosis is often characterized by co-evolutionary changes in the genomes of the partners involved. An understanding of these changes can provide insight into the nature of the relationship, including the mechanisms that initiate and maintain an association between organisms. In this study we examined the genome sequences of bacteria isolated from the Drosophila melanogaster gut with the objective of identifying genes that are important for function in the host. We compared microbiota isolates with con-specific or closely related bacterial species isolated from non-fly environments. First the phenotype of germ-free Drosophila (axenic flies) was compared to that of flies colonized with specific bacteria (gnotobiotic flies) as a measure of symbiotic function. Non-fly isolates were functionally distinct from bacteria isolated from flies, conferring slower development and an altered nutrient profile in the host, traits known to be microbiota-dependent. Comparative genomic methods were next employed to identify putative symbiosis factors: genes found in bacteria that restore microbiota-dependent traits to gnotobiotic flies, but absent from those that do not. Factors identified include riboflavin synthesis and stress resistance. We also used a phylogenomic approach to identify protein coding genes for which fly-isolate sequences were more similar to each other than to other sequences, reasoning that these genes may have a shared function unique to the fly environment. This method identified genes in Acetobacter species that cluster in two distinct genomic loci: one predicted to be involved in oxidative stress detoxification and another encoding an efflux pump. In summary, we leveraged genomic and in vivo functional comparisons to identify candidate traits that distinguish symbiotic bacteria. These candidates can serve as the basis for further work investigating the genetic requirements of bacteria for function and persistence in the Drosophila gut.

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          Most cited references43

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          The Toll-like receptor 2 pathway establishes colonization by a commensal of the human microbiota.

          Mucosal surfaces constantly encounter microbes. Toll-like receptors (TLRs) mediate recognition of microbial patterns to eliminate pathogens. By contrast, we demonstrate that the prominent gut commensal Bacteroides fragilis activates the TLR pathway to establish host-microbial symbiosis. TLR2 on CD4(+) T cells is required for B. fragilis colonization of a unique mucosal niche in mice during homeostasis. A symbiosis factor (PSA, polysaccharide A) of B. fragilis signals through TLR2 directly on Foxp3(+) regulatory T cells to promote immunologic tolerance. B. fragilis lacking PSA is unable to restrain T helper 17 cell responses and is defective in niche-specific mucosal colonization. Therefore, commensal bacteria exploit the TLR pathway to actively suppress immunity. We propose that the immune system can discriminate between pathogens and the microbiota through recognition of symbiotic bacterial molecules in a process that engenders commensal colonization.
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            Extreme genome reduction in symbiotic bacteria.

            Since 2006, numerous cases of bacterial symbionts with extraordinarily small genomes have been reported. These organisms represent independent lineages from diverse bacterial groups. They have diminutive gene sets that rival some mitochondria and chloroplasts in terms of gene numbers and lack genes that are considered to be essential in other bacteria. These symbionts have numerous features in common, such as extraordinarily fast protein evolution and a high abundance of chaperones. Together, these features point to highly degenerate genomes that retain only the most essential functions, often including a considerable fraction of genes that serve the hosts. These discoveries have implications for the concept of minimal genomes, the origins of cellular organelles, and studies of symbiosis and host-associated microbiota.
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              Multiorganismal insects: diversity and function of resident microorganisms.

              All insects are colonized by microorganisms on the insect exoskeleton, in the gut and hemocoel, and within insect cells. The insect microbiota is generally different from microorganisms in the external environment, including ingested food. Specifically, certain microbial taxa are favored by the conditions and resources in the insect habitat, by their tolerance of insect immunity, and by specific mechanisms for their transmission. The resident microorganisms can promote insect fitness by contributing to nutrition, especially by providing essential amino acids, B vitamins, and, for fungal partners, sterols. Some microorganisms protect their insect hosts against pathogens, parasitoids, and other parasites by synthesizing specific toxins or modifying the insect immune system. Priorities for future research include elucidation of microbial contributions to detoxification, especially of plant allelochemicals in phytophagous insects, and resistance to pathogens; as well as their role in among-insect communication; and the potential value of manipulation of the microbiota to control insect pests.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                04 November 2014
                2014
                : 5
                : 576
                Affiliations
                [1] 1Department of Entomology, Cornell University Ithaca, NY, USA
                [2] 2Department of Nutritional Science, Cornell University Ithaca, NY, USA
                [3] 3Department of Microbiology, Cornell University Ithaca, NY, USA
                [4] 4Department of Biology, Mansfield University Mansfield, PA, USA
                [5] 5Department of Molecular Biology and Genetics, Cornell University Ithaca, NY, USA
                Author notes

                Edited by: Ute Hentschel, University of Wuerzburg, Germany

                Reviewed by: Ute Hentschel, University of Wuerzburg, Germany; James Angus Chandler, California Academy of Sciences, USA; Philipp Engel, University of Lausanne, Switzerland

                *Correspondence: Peter D. Newell, Department of Biological Sciences, 335 Shineman Center, Oswego State University of New York, Oswego, NY 13126, USA e-mail: peter.newell@ 123456oswego.edu

                This article was submitted to Microbial Symbioses, a section of the journal Frontiers in Microbiology.

                †Present address: Peter D. Newell, 335 Shineman Center, Oswego State University of New York, Oswego, USA

                John M. Chaston, Department of Plant and Wildlife Sciences, Genetics and Biotechnology, Brigham Young University, Provo, USA

                Adam C. N. Wong, Charles Perkins Centre, School of Biological Sciences, University of Sydney, Sydney, Australia

                Adam J. Dobson, Department of Genetics, Evolution and Environment, Institute of Healthy Ageing, University College London, London, UK

                Article
                10.3389/fmicb.2014.00576
                4219406
                25408687
                786aebd1-ccc7-42cc-8f22-bbc30dc6a7df
                Copyright © 2014 Newell, Chaston, Wang, Winans, Sannino, Wong, Dobson, Kagle and Douglas.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 23 June 2014
                : 13 October 2014
                Page count
                Figures: 3, Tables: 7, Equations: 0, References: 66, Pages: 15, Words: 11443
                Categories
                Microbiology
                Original Research Article

                Microbiology & Virology
                microbiome,symbiosis,genome,acetobacter,lactobacillus
                Microbiology & Virology
                microbiome, symbiosis, genome, acetobacter, lactobacillus

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