Topical Glaucoma Therapy Is Associated With Alterations of the Ocular Surface Microbiome
To investigate the ocular surface microbiome of patients with unilateral or asymmetric glaucoma being treated with topical ophthalmic medications in one eye and to determine whether microbial community changes were related to measures of ocular surface disease.PurposeTo investigate the ocular surfac...
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Published in | Investigative ophthalmology & visual science Vol. 63; no. 9; p. 32 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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The Association for Research in Vision and Ophthalmology
29.08.2022
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ISSN | 1552-5783 0146-0404 1552-5783 |
DOI | 10.1167/iovs.63.9.32 |
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Abstract | To investigate the ocular surface microbiome of patients with unilateral or asymmetric glaucoma being treated with topical ophthalmic medications in one eye and to determine whether microbial community changes were related to measures of ocular surface disease.PurposeTo investigate the ocular surface microbiome of patients with unilateral or asymmetric glaucoma being treated with topical ophthalmic medications in one eye and to determine whether microbial community changes were related to measures of ocular surface disease.V3-V4 16S rRNA sequencing was conducted on ocular surface swabs collected from both eyes of 17 subjects: 10 patients with asymmetric/unilateral glaucoma using topical glaucoma therapy on only one eye and seven age-matched, healthy controls with no history of ocular disease or eyedrop use. Samples were categorized into three groups: patients' glaucomatous eye treated with eyedrops, patients' contralateral eye without eyedrops, and healthy control eyes. Comparisons were made for microbial diversity and composition, with differences in composition tested for association with ocular surface disease measures including tear meniscus height, tear break-up time, and Dry Eye Questionnaire.MethodsV3-V4 16S rRNA sequencing was conducted on ocular surface swabs collected from both eyes of 17 subjects: 10 patients with asymmetric/unilateral glaucoma using topical glaucoma therapy on only one eye and seven age-matched, healthy controls with no history of ocular disease or eyedrop use. Samples were categorized into three groups: patients' glaucomatous eye treated with eyedrops, patients' contralateral eye without eyedrops, and healthy control eyes. Comparisons were made for microbial diversity and composition, with differences in composition tested for association with ocular surface disease measures including tear meniscus height, tear break-up time, and Dry Eye Questionnaire.Samples obtained from the patients' treated and untreated eyes both had significantly greater alpha-diversity and relative abundance of gram-negative organisms compared to healthy controls. The microbial composition of patient eyes was associated with decreased tear meniscus height and tear break-up time, whereas metagenomic predictions, based on 16S rRNA data, suggested increased synthesis of lipopolysaccharide.ResultsSamples obtained from the patients' treated and untreated eyes both had significantly greater alpha-diversity and relative abundance of gram-negative organisms compared to healthy controls. The microbial composition of patient eyes was associated with decreased tear meniscus height and tear break-up time, whereas metagenomic predictions, based on 16S rRNA data, suggested increased synthesis of lipopolysaccharide.The ocular surface microbiome of patients taking unilateral preserved glaucoma drops is characterized by a highly diverse array of gram-negative bacteria that is significantly different from the predominantly gram-positive microbes detected on healthy control eyes. These compositional differences were associated with decreased tear film measures and distinct inferred protein synthesis pathways, suggesting a potential link between microbial alterations and ocular surface inflammation.ConclusionsThe ocular surface microbiome of patients taking unilateral preserved glaucoma drops is characterized by a highly diverse array of gram-negative bacteria that is significantly different from the predominantly gram-positive microbes detected on healthy control eyes. These compositional differences were associated with decreased tear film measures and distinct inferred protein synthesis pathways, suggesting a potential link between microbial alterations and ocular surface inflammation. |
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AbstractList | To investigate the ocular surface microbiome of patients with unilateral or asymmetric glaucoma being treated with topical ophthalmic medications in one eye and to determine whether microbial community changes were related to measures of ocular surface disease.PurposeTo investigate the ocular surface microbiome of patients with unilateral or asymmetric glaucoma being treated with topical ophthalmic medications in one eye and to determine whether microbial community changes were related to measures of ocular surface disease.V3-V4 16S rRNA sequencing was conducted on ocular surface swabs collected from both eyes of 17 subjects: 10 patients with asymmetric/unilateral glaucoma using topical glaucoma therapy on only one eye and seven age-matched, healthy controls with no history of ocular disease or eyedrop use. Samples were categorized into three groups: patients' glaucomatous eye treated with eyedrops, patients' contralateral eye without eyedrops, and healthy control eyes. Comparisons were made for microbial diversity and composition, with differences in composition tested for association with ocular surface disease measures including tear meniscus height, tear break-up time, and Dry Eye Questionnaire.MethodsV3-V4 16S rRNA sequencing was conducted on ocular surface swabs collected from both eyes of 17 subjects: 10 patients with asymmetric/unilateral glaucoma using topical glaucoma therapy on only one eye and seven age-matched, healthy controls with no history of ocular disease or eyedrop use. Samples were categorized into three groups: patients' glaucomatous eye treated with eyedrops, patients' contralateral eye without eyedrops, and healthy control eyes. Comparisons were made for microbial diversity and composition, with differences in composition tested for association with ocular surface disease measures including tear meniscus height, tear break-up time, and Dry Eye Questionnaire.Samples obtained from the patients' treated and untreated eyes both had significantly greater alpha-diversity and relative abundance of gram-negative organisms compared to healthy controls. The microbial composition of patient eyes was associated with decreased tear meniscus height and tear break-up time, whereas metagenomic predictions, based on 16S rRNA data, suggested increased synthesis of lipopolysaccharide.ResultsSamples obtained from the patients' treated and untreated eyes both had significantly greater alpha-diversity and relative abundance of gram-negative organisms compared to healthy controls. The microbial composition of patient eyes was associated with decreased tear meniscus height and tear break-up time, whereas metagenomic predictions, based on 16S rRNA data, suggested increased synthesis of lipopolysaccharide.The ocular surface microbiome of patients taking unilateral preserved glaucoma drops is characterized by a highly diverse array of gram-negative bacteria that is significantly different from the predominantly gram-positive microbes detected on healthy control eyes. These compositional differences were associated with decreased tear film measures and distinct inferred protein synthesis pathways, suggesting a potential link between microbial alterations and ocular surface inflammation.ConclusionsThe ocular surface microbiome of patients taking unilateral preserved glaucoma drops is characterized by a highly diverse array of gram-negative bacteria that is significantly different from the predominantly gram-positive microbes detected on healthy control eyes. These compositional differences were associated with decreased tear film measures and distinct inferred protein synthesis pathways, suggesting a potential link between microbial alterations and ocular surface inflammation. |
Author | Somohano, Karina Uhlemann, Anne-Catrin Al-Aswad, Lama A. Winn, Bryan J. Chang, Chih-Chiun J. Liebmann, Jeffrey Cioffi, George A. Lynch, Susan V. Zemsky, Christine |
Author_xml | – sequence: 1 givenname: Chih-Chiun J. surname: Chang fullname: Chang, Chih-Chiun J. organization: Department of Ophthalmology, University of California San Francisco, San Francisco, California, United States – sequence: 2 givenname: Karina surname: Somohano fullname: Somohano, Karina organization: Department of Ophthalmology, Columbia University Medical Center, New York-Presbyterian Hospital, New York, New York, United States – sequence: 3 givenname: Christine surname: Zemsky fullname: Zemsky, Christine organization: Department of Ophthalmology, Columbia University Medical Center, New York-Presbyterian Hospital, New York, New York, United States – sequence: 4 givenname: Anne-Catrin surname: Uhlemann fullname: Uhlemann, Anne-Catrin organization: Department of Internal Medicine, Division of Infectious Disease, Columbia University Medical Center, New York-Presbyterian Hospital, New York, New York, United States – sequence: 5 givenname: Jeffrey surname: Liebmann fullname: Liebmann, Jeffrey organization: Department of Ophthalmology, Columbia University Medical Center, New York-Presbyterian Hospital, New York, New York, United States – sequence: 6 givenname: George A. surname: Cioffi fullname: Cioffi, George A. organization: Department of Ophthalmology, Columbia University Medical Center, New York-Presbyterian Hospital, New York, New York, United States – sequence: 7 givenname: Lama A. surname: Al-Aswad fullname: Al-Aswad, Lama A. organization: Department of Ophthalmology, Columbia University Medical Center, New York-Presbyterian Hospital, New York, New York, United States, Department of Ophthalmology, New York University Langone Health, New York, New York, United States – sequence: 8 givenname: Susan V. surname: Lynch fullname: Lynch, Susan V. organization: Division of Gastroenterology, Department of Medicine, University of California, San Francisco, San Francisco, California, United States – sequence: 9 givenname: Bryan J. surname: Winn fullname: Winn, Bryan J. organization: Department of Ophthalmology, University of California San Francisco, San Francisco, California, United States, Department of Ophthalmology, Columbia University Medical Center, New York-Presbyterian Hospital, New York, New York, United States, Ophthalmology Section, Surgical Service, San Francisco Veterans Affairs Medical Center, San Francisco, California, United States |
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Title | Topical Glaucoma Therapy Is Associated With Alterations of the Ocular Surface Microbiome |
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