Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pone.0201768
DC Field | Value | |
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dc.title | Human pharyngeal microbiota in age-related macular degeneration | |
dc.contributor.author | Ho E.X.P. | |
dc.contributor.author | Cheung C.M.G. | |
dc.contributor.author | Sim S. | |
dc.contributor.author | Chu C.W. | |
dc.contributor.author | Wilm A. | |
dc.contributor.author | Lin C.B. | |
dc.contributor.author | Mathur R. | |
dc.contributor.author | Wong D. | |
dc.contributor.author | Chan C.M. | |
dc.contributor.author | Bhagarva M. | |
dc.contributor.author | Laude A. | |
dc.contributor.author | Lim T.H. | |
dc.contributor.author | Wong T.Y. | |
dc.contributor.author | Cheng C.Y. | |
dc.contributor.author | Davila S. | |
dc.contributor.author | Hibberd M. | |
dc.date.accessioned | 2020-03-23T06:19:32Z | |
dc.date.available | 2020-03-23T06:19:32Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | Ho E.X.P., Cheung C.M.G., Sim S., Chu C.W., Wilm A., Lin C.B., Mathur R., Wong D., Chan C.M., Bhagarva M., Laude A., Lim T.H., Wong T.Y., Cheng C.Y., Davila S., Hibberd M. (2018). Human pharyngeal microbiota in age-related macular degeneration. PLoS ONE 13 (8) : e0201768. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0201768 | |
dc.identifier.issn | 19326203 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/165897 | |
dc.description.abstract | Background While the aetiology of age-related macular degeneration (AMD)—a major blinding disease —remains unknown, the disease is strongly associated with variants in the complement factor H (CFH) gene. CFH variants also confer susceptibility to invasive infection with several bacterial colonizers of the nasopharyngeal mucosa. This shared susceptibility locus implicates complement deregulation as a common disease mechanism, and suggests the possibility that microbial interactions with host complement may trigger AMD. In this study, we address this possibility by testing the hypothesis that AMD is associated with specific microbial colonization of the human nasopharynx. Results High-throughput Illumina sequencing of the V3-V6 region of the microbial 16S ribosomal RNA gene was used to comprehensively and accurately describe the human pharyngeal microbiome, at genus level, in 245 AMD patients and 386 controls. Based on mean and differential microbial abundance analyses, we determined an overview of the pharyngeal microbiota, as well as candidate genera (Prevotella and Gemella) suggesting an association towards AMD health and disease conditions. Conclusions Utilizing an extensive study population from Singapore, our results provided an accurate description of the pharyngeal microbiota profiles in AMD health and disease conditions. Through identification of candidate genera that are different between conditions, we provide preliminary evidence for the existence of microbial triggers for AMD. Ethical approval for this study was obtained through the Singapore Health Clinical Institutional Review Board, reference numbers R799/63/2010 and 2010/585/A. © 2018 Ho et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | |
dc.publisher | Public Library of Science | |
dc.source | Unpaywall 20200320 | |
dc.subject | RNA 16S | |
dc.subject | bacterial RNA | |
dc.subject | 16S ribosomal RNA gene | |
dc.subject | adult | |
dc.subject | age related macular degeneration | |
dc.subject | Article | |
dc.subject | controlled study | |
dc.subject | disease association | |
dc.subject | female | |
dc.subject | Gemella | |
dc.subject | high throughput sequencing | |
dc.subject | human | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | microbial colonization | |
dc.subject | microflora | |
dc.subject | middle aged | |
dc.subject | nasopharynx | |
dc.subject | nonhuman | |
dc.subject | pathogenesis | |
dc.subject | Prevotella | |
dc.subject | RNA gene | |
dc.subject | RNA sequence | |
dc.subject | Singapore | |
dc.subject | aged | |
dc.subject | case control study | |
dc.subject | cohort analysis | |
dc.subject | genetics | |
dc.subject | macular degeneration | |
dc.subject | microbiology | |
dc.subject | nose cavity | |
dc.subject | pharynx | |
dc.subject | very elderly | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Aged, 80 and over | |
dc.subject | Case-Control Studies | |
dc.subject | Cohort Studies | |
dc.subject | Female | |
dc.subject | Humans | |
dc.subject | Macular Degeneration | |
dc.subject | Male | |
dc.subject | Microbiota | |
dc.subject | Middle Aged | |
dc.subject | Nasal Cavity | |
dc.subject | Pharynx | |
dc.subject | RNA, Bacterial | |
dc.subject | RNA, Ribosomal, 16S | |
dc.subject | Singapore | |
dc.type | Article | |
dc.contributor.department | DUKE-NUS MEDICAL SCHOOL | |
dc.contributor.department | MICROBIOLOGY AND IMMUNOLOGY | |
dc.description.doi | 10.1371/journal.pone.0201768 | |
dc.description.sourcetitle | PLoS ONE | |
dc.description.volume | 13 | |
dc.description.issue | 8 | |
dc.description.page | e0201768 | |
Appears in Collections: | Elements Staff Publications |
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