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      Microbiome of the paranasal sinuses: Update and literature review

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          Abstract

          Background:

          Our understanding of the resident microbiome of the paranasal sinuses has changed considerably in recent years. Once presumed to be sterile, healthy sinus cavities are now known to harbor a diverse assemblage of microorganisms, and, it is hypothesized that alterations in the kinds and quantities of these microbes may play a role in the pathogenesis of chronic rhinosinusitis (CRS).

          Objectives:

          To review the current literature regarding the sinus microbiome and collate research findings from relevant studies published to date.

          Methods:

          A systematic literature review was performed on all molecular studies that investigated the microbial communities of the paranasal sinuses. Methods of detection, microbiome composition, and comparative profiling between patients with and without CRS were explored.

          Results:

          A complex consortium of microorganisms has been demonstrated in the sinuses of both patients with and without CRS. However, the latter generally have been characterized by reduced biodiversity compared with controls, with selective enrichment of particular microbes (e.g., Staphylococcus aureus). Such disruptions in the resident microbiome may contribute to disease pathogenesis by enhancing the virulence of potential pathogens and adversely modulating immune responses.

          Conclusion:

          The advent of culture-independent molecular approaches has led to a greater appreciation of the intricate microbial ecology of the paranasal sinuses. Microbiota composition, distribution, and abundance impact mucosal health and influence pathogen growth and function. A deeper understanding of the host-microbiome relationship and its constituents may encourage development of new treatment paradigms for CRS, which target restoration of microbiome homeostasis and cultivation of optimal microbial communities.

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          Most cited references68

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          Inflammatory bowel disease.

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            Error-correcting barcoded primers for pyrosequencing hundreds of samples in multiplex.

            We constructed error-correcting DNA barcodes that allow one run of a massively parallel pyrosequencer to process up to 1,544 samples simultaneously. Using these barcodes we processed bacterial 16S rRNA gene sequences representing microbial communities in 286 environmental samples, corrected 92% of sample assignment errors, and thus characterized nearly as many 16S rRNA genes as have been sequenced to date by Sanger sequencing.
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              A molecular view of microbial diversity and the biosphere.

              N Pace (1997)
              Over three decades of molecular-phylogenetic studies, researchers have compiled an increasingly robust map of evolutionary diversification showing that the main diversity of life is microbial, distributed among three primary relatedness groups or domains: Archaea, Bacteria, and Eucarya. The general properties of representatives of the three domains indicate that the earliest life was based on inorganic nutrition and that photosynthesis and use of organic compounds for carbon and energy metabolism came comparatively later. The application of molecular-phylogenetic methods to study natural microbial ecosystems without the traditional requirement for cultivation has resulted in the discovery of many unexpected evolutionary lineages; members of some of these lineages are only distantly related to known organisms but are sufficiently abundant that they are likely to have impact on the chemistry of the biosphere.
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                Author and article information

                Journal
                Am J Rhinol Allergy
                Am J Rhinol Allergy
                rhinol
                American Journal of Rhinology & Allergy
                OceanSide Publications, Inc. (Providence, RIUSA )
                1945-8924
                1945-8932
                Jan-Feb 2016
                : 30
                : 1
                : 3-16
                Affiliations
                [1]From the 1Department of Otolaryngology-Head and Neck Surgery, Orange County Sinus Institute, Southern California Permanente Medical Group, Irvine, California,
                [2] 2Department of Head and Neck Surgery, David Geffen School of Medicine at the University of California Los Angeles, Los Angeles, California,
                [3] 3Division of Infectious Diseases, Department of Medicine, University of Colorado Denver, Aurora, Colorado, and
                [4] 4Department of Otolaryngology—Head and Neck Surgery, University of Colorado Denver, Aurora, Colorado
                Author notes
                Address correspondence to Jivianne T. Lee, M.D., Department of Otolaryngology-Head and Neck Surgery, 6670 Alton Parkway, Irvine, CA 92618 E-mail address: jivianne@ 123456gmail.com
                Article
                AJRA091-15
                10.2500/ajra.2016.30.4255
                5517778
                26867525
                38eaadbe-dcd0-462e-90ca-0b964db15c88
                Copyright © 2016, OceanSide Publications, Inc., U.S.A.

                This publication is provided under the terms of the Creative Commons Public License ("CCPL" or "License"), in attribution 3.0 unported, further described at http://creativecommons.org/license/by/3.0/legalcode. The work is protected by copyright and/or other applicable law. Any use of the work other then as authorized under this license or copyright law is prohibited

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                Categories
                Articles

                Immunology
                microbiome,paranasal,sinuses,chronic rhinosinusitis,bacteria,diversity,community,culture-independent microbiology

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