Local oral and nasal microbiome diversity in age-related macular degeneration.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
02 03 2020
Historique:
received: 12 07 2019
accepted: 11 02 2020
entrez: 4 3 2020
pubmed: 4 3 2020
medline: 13 11 2020
Statut: epublish

Résumé

Age-related macular degeneration (AMD) is a chronic degenerative disease of the retina. Recent reports have highlighted the potential role of mucosal surface microbes in the pathogenesis of AMD. In this case-control study, the composition of the nasal and oral microbiota in newly diagnosed neovascular age-related macular degeneration cases (6 male, 7 female) was compared to controls without retinal diseases (2 male, 3 female). PCR amplification of 16S rRNA genes was performed with universal primers amplifying the V4 variable region (515F-806R). Distinct microbial community characterization was achieved using Principal Coordinates Analysis (PCoA) of the Bray-Curtis index with comparative analysis between cases and controls performed within QIIME 2. Sequencing of all cases and controls revealed clear separation with strong beta diversity between oral and nasal microbial communities (p < 0.001). Microbial composition differed between cases and controls in both oral and nasal samples. The top three oral microbes identified as different compared to controls included Burkholderiales (7.41 log2fold change, p = 3.29E-05), Actinomyceataceae (6.22 log2fold change, p = 3.73E-06) and Gemella (5.28 log2fold change, p = 0.0002). The top three nasal microbes identified as different compared to controls included Rothia (13.6 log2fold change, p =  3.63E-18), Actinobacteria (10.29 log2fold change, p = 9.81E-10) and Propionibacteriales (8.73 log2fold change, p = 6.74E-09). These relative shifts in communities of bacteria detected in newly diagnosed neovascular AMD patients may suggest additional mechanistic links in disease pathogenesis.

Identifiants

pubmed: 32123200
doi: 10.1038/s41598-020-60674-3
pii: 10.1038/s41598-020-60674-3
pmc: PMC7052252
doi:

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3862

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Auteurs

Jacob Rullo (J)

Queen's University, Kingston Health Sciences Center, Department of Ophthalmology, 166 Brock Street, Kingston, Ontario, K7L 5G2, Canada. jrullo@qmed.ca.

Parsa Mehraban Far (PM)

Queen's University, Kingston Health Sciences Center, Department of Ophthalmology, 166 Brock Street, Kingston, Ontario, K7L 5G2, Canada.

Matthew Quinn (M)

Queen's University, Kingston Health Sciences Center, Department of Ophthalmology, 166 Brock Street, Kingston, Ontario, K7L 5G2, Canada.

Neel Sharma (N)

Queen's University, Kingston Health Sciences Center, Department of Ophthalmology, 166 Brock Street, Kingston, Ontario, K7L 5G2, Canada.

Steven Bae (S)

Queen's University, Kingston Health Sciences Center, Department of Ophthalmology, 166 Brock Street, Kingston, Ontario, K7L 5G2, Canada.

Isabella Irrcher (I)

Queen's University, Kingston Health Sciences Center, Department of Ophthalmology, 166 Brock Street, Kingston, Ontario, K7L 5G2, Canada.

Sanjay Sharma (S)

Queen's University, Kingston Health Sciences Center, Department of Ophthalmology, 166 Brock Street, Kingston, Ontario, K7L 5G2, Canada.

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