97
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Human Skin Fungal Diversity

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Traditional culture-based methods have incompletely defined the etiology of common recalcitrant human fungal skin diseases including athlete’s foot and toenail infections. Skin protects humans from invasion by pathogenic microorganisms, while providing a home for diverse commensal microbiota 1 . Bacterial genomic sequence data have generated novel hypotheses about species and community structures underlying human disorders 2, 3, 4 . However, microbial diversity is not limited to bacteria; microorganisms such as fungi also play major roles in microbial community stability, human health and disease 5 . Genomic methodologies to identify fungal species and communities have been limited compared with tools available for bacteria 6 . Fungal evolution can be reconstructed with phylogenetic markers, including ribosomal RNA gene regions and other highly conserved genes 7 . Here, we sequenced and analyzed fungal communities of 14 skin sites in 10 healthy adults. Eleven core body and arm sites were dominated by Malassezia fungi, with species-level classifications revealing greater topographical resolution between sites. By contrast, three foot sites, plantar heel, toenail, and toeweb, exhibited tremendous fungal diversity. Concurrent analysis of bacterial and fungal communities demonstrated that skin physiologic attributes and topography differentially shape these two microbial communities. These results provide a framework for future investigation of interactions between pathogenic and commensal fungal and bacterial communities in maintaining human health and contributing to disease pathogenesis.

          Related collections

          Most cited references21

          • Record: found
          • Abstract: found
          • Article: not found

          Interactions between commensal fungi and the C-type lectin receptor Dectin-1 influence colitis.

          The intestinal microflora, typically equated with bacteria, influences diseases such as obesity and inflammatory bowel disease. Here, we show that the mammalian gut contains a rich fungal community that interacts with the immune system through the innate immune receptor Dectin-1. Mice lacking Dectin-1 exhibited increased susceptibility to chemically induced colitis, which was the result of altered responses to indigenous fungi. In humans, we identified a polymorphism in the gene for Dectin-1 (CLEC7A) that is strongly linked to a severe form of ulcerative colitis. Together, our findings reveal a eukaryotic fungal community in the gut (the "mycobiome") that coexists with bacteria and substantially expands the repertoire of organisms interacting with the intestinal immune system to influence health and disease.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            The human microbiome: our second genome.

            The human genome has been referred to as the blueprint of human biology. In this review we consider an essential but largely ignored overlay to that blueprint, the human microbiome, which is composed of those microbes that live in and on our bodies. The human microbiome is a source of genetic diversity, a modifier of disease, an essential component of immunity, and a functional entity that influences metabolism and modulates drug interactions. Characterization and analysis of the human microbiome have been greatly catalyzed by advances in genomic technologies. We discuss how these technologies have shaped this emerging field of study and advanced our understanding of the human microbiome. We also identify future challenges, many of which are common to human genetic studies, and predict that in the future, analyzing genetic variation and risk of human disease will sometimes necessitate the integration of human and microbial genomic data sets.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Medically important bacterial-fungal interactions.

              Whether it is in the setting of disease or in a healthy state, the human body contains a diverse range of microorganisms, including bacteria and fungi. The interactions between these taxonomically diverse microorganisms are highly dynamic and dependent on a multitude of microorganism and host factors. Human disease can develop from an imbalance between commensal bacteria and fungi or from invasion of particular host niches by opportunistic bacterial and fungal pathogens. This Review describes the clinical and molecular characteristics of bacterial-fungal interactions that are relevant to human disease.
                Bookmark

                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                9 May 2013
                22 May 2013
                20 June 2013
                20 December 2013
                : 498
                : 7454
                : 367-370
                Affiliations
                [1 ]Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892
                [2 ]Dermatology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892
                [3 ]NIH Intramural Sequencing Center, National Human Genome Research Institute, Rockville, MD 20852
                Author notes
                *
                Corresponding authors: Julia A. Segre, National Human Genome Research Institute, Genetics and Molecular Biology Branch, Building 49, Room 4A26, 49 Convent Dr, MSC 4442, Bethesda, MD 20892-4442, jsegre@ 123456nhgri.nih.gov , Phone: (301) 402-2314, Fax: (301) 402-4929. Heidi H. Kong, Dermatology Branch, Center for Cancer Research, National Cancer Institute, Building 10, Room 12N238, 10 Center Dr, MSC 1908, Bethesda, MD 20892-1908, konghe@ 123456mail.nih.gov , Phone: (301) 402-7452, Fax: (301) 496-5370
                [†]

                These authors contributed equally.

                Article
                NIHMS466260
                10.1038/nature12171
                3711185
                23698366
                133fd49b-f38a-4b6f-a6f9-8204dc93eb81

                Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms

                History
                Funding
                Funded by: National Human Genome Research Institute : NHGRI
                Award ID: ZIA HG000180-12 || HG
                Categories
                Article

                Uncategorized
                fungi,genome,skin,dermatology,microbiome,malassezia,its,18s rrna
                Uncategorized
                fungi, genome, skin, dermatology, microbiome, malassezia, its, 18s rrna

                Comments

                Comment on this article