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      Skin and gut microbiomes of a wild mammal respond to different environmental cues

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          Abstract

          Background

          Animal skin and gut microbiomes are important components of host fitness. However, the processes that shape the microbiomes of wildlife are poorly understood, particularly with regard to exposure to environmental contaminants. We used 16S rRNA amplicon sequencing to quantify how exposure to radionuclides impacts the skin and gut microbiota of a small mammal, the bank vole Myodes glareolus, inhabiting areas within and outside the Chernobyl Exclusion Zone (CEZ), Ukraine.

          Results

          Skin microbiomes of male bank voles were more diverse than females. However, the most pronounced differences in skin microbiomes occurred at a larger spatial scale, with higher alpha diversity in the skin microbiomes of bank voles from areas within the CEZ, whether contaminated by radionuclides or not, than in the skin microbiomes of animals from uncontaminated locations outside the CEZ, near Kyiv. Similarly, irrespective of the level of radionuclide contamination, skin microbiome communities (beta diversity) showed greater similarities within the CEZ, than to the areas near Kyiv. Hence, bank vole skin microbiome communities are structured more by geography than the level of soil radionuclides. This pattern presents a contrast with bank vole gut microbiota, where microbiomes could be strikingly similar among distant (~ 80 km of separation), uncontaminated locations, and where differences in microbiome community structure were associated with the level of radioactivity. We also found that the level of (dis)similarity between the skin and gut microbiome communities from the same individuals was contingent on the potential for exposure to radionuclides.

          Conclusions

          Bank vole skin and gut microbiomes have distinct responses to similar environmental cues and thus are structured at different spatial scales. Our study shows how exposure to environmental pollution can affect the relationship between a mammalian host’s skin and gut microbial communities, potentially homogenising the microbiomes in habitats affected by pollution.

          Electronic supplementary material

          The online version of this article (10.1186/s40168-018-0595-0) contains supplementary material, which is available to authorized users.

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          Most cited references53

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          Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample.

          The ongoing revolution in high-throughput sequencing continues to democratize the ability of small groups of investigators to map the microbial component of the biosphere. In particular, the coevolution of new sequencing platforms and new software tools allows data acquisition and analysis on an unprecedented scale. Here we report the next stage in this coevolutionary arms race, using the Illumina GAIIx platform to sequence a diverse array of 25 environmental samples and three known "mock communities" at a depth averaging 3.1 million reads per sample. We demonstrate excellent consistency in taxonomic recovery and recapture diversity patterns that were previously reported on the basis of metaanalysis of many studies from the literature (notably, the saline/nonsaline split in environmental samples and the split between host-associated and free-living communities). We also demonstrate that 2,000 Illumina single-end reads are sufficient to recapture the same relationships among samples that we observe with the full dataset. The results thus open up the possibility of conducting large-scale studies analyzing thousands of samples simultaneously to survey microbial communities at an unprecedented spatial and temporal resolution.
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            The microbiome and innate immunity.

            The intestinal microbiome is a signalling hub that integrates environmental inputs, such as diet, with genetic and immune signals to affect the host's metabolism, immunity and response to infection. The haematopoietic and non-haematopoietic cells of the innate immune system are located strategically at the host-microbiome interface. These cells have the ability to sense microorganisms or their metabolic products and to translate the signals into host physiological responses and the regulation of microbial ecology. Aberrations in the communication between the innate immune system and the gut microbiota might contribute to complex diseases.
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              How glycan metabolism shapes the human gut microbiota.

              Symbiotic microorganisms that reside in the human intestine are adept at foraging glycans and polysaccharides, including those in dietary plants (starch, hemicellulose and pectin), animal-derived cartilage and tissue (glycosaminoglycans and N-linked glycans), and host mucus (O-linked glycans). Fluctuations in the abundance of dietary and endogenous glycans, combined with the immense chemical variation among these molecules, create a dynamic and heterogeneous environment in which gut microorganisms proliferate. In this Review, we describe how glycans shape the composition of the gut microbiota over various periods of time, the mechanisms by which individual microorganisms degrade these glycans, and potential opportunities to intentionally influence this ecosystem for better health and nutrition.
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                Author and article information

                Contributors
                +358 44 9251411 , anton.lavrinienko@oulu.fi
                yevhen.tukalenko@oulu.fi
                tapio.mappes@jyu.fi
                phillip.watts@oulu.fi
                Journal
                Microbiome
                Microbiome
                Microbiome
                BioMed Central (London )
                2049-2618
                26 November 2018
                26 November 2018
                2018
                : 6
                : 209
                Affiliations
                [1 ]ISNI 0000 0001 0941 4873, GRID grid.10858.34, Department of Ecology and Genetics, , University of Oulu, ; 90570 Oulu, Finland
                [2 ]ISNI 0000 0004 0385 8248, GRID grid.34555.32, Institute of Biology and Medicine, , Taras Shevchenko National University of Kyiv, ; Kyiv, 03022 Ukraine
                [3 ]ISNI 0000 0001 1013 7965, GRID grid.9681.6, Department of Biological and Environmental Science, , University of Jyväskylä, ; 40014 Jyväskylä, Finland
                Author information
                http://orcid.org/0000-0002-9524-8054
                Article
                595
                10.1186/s40168-018-0595-0
                6258405
                30477569
                cd001975-3185-47fc-ad60-a95458627726
                © The Author(s). 2018

                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. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 22 June 2018
                : 14 November 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100005876, Biotieteiden ja Ympäristön Tutkimuksen Toimikunta;
                Award ID: 287153
                Award ID: 268670
                Award Recipient :
                Funded by: Tutkijakoulu, Oulun Yliopiston (FI)
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                anthropogenic impact,biodiversity,ionising radiation,pollution,skin microbiome,wild mammal

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