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Corneal Infection Models: Tools to Investigate the Role of Biofilms in Bacterial Keratitis
Bacterial keratitis is a corneal infection which may cause visual impairment or even loss of the infected eye. It remains a major cause of blindness in the developing world. Staphylococcus aureus and Pseudomonas aeruginosa are common causative agents and these bacterial species are known to colonise...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696224/ https://www.ncbi.nlm.nih.gov/pubmed/33182687 http://dx.doi.org/10.3390/cells9112450 |
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author | Urwin, Lucy Okurowska, Katarzyna Crowther, Grace Roy, Sanhita Garg, Prashant Karunakaran, Esther MacNeil, Sheila Partridge, Lynda J. Green, Luke R. Monk, Peter N. |
author_facet | Urwin, Lucy Okurowska, Katarzyna Crowther, Grace Roy, Sanhita Garg, Prashant Karunakaran, Esther MacNeil, Sheila Partridge, Lynda J. Green, Luke R. Monk, Peter N. |
author_sort | Urwin, Lucy |
collection | PubMed |
description | Bacterial keratitis is a corneal infection which may cause visual impairment or even loss of the infected eye. It remains a major cause of blindness in the developing world. Staphylococcus aureus and Pseudomonas aeruginosa are common causative agents and these bacterial species are known to colonise the corneal surface as biofilm populations. Biofilms are complex bacterial communities encased in an extracellular polymeric matrix and are notoriously difficult to eradicate once established. Biofilm bacteria exhibit different phenotypic characteristics from their planktonic counterparts, including an increased resistance to antibiotics and the host immune response. Therefore, understanding the role of biofilms will be essential in the development of new ophthalmic antimicrobials. A brief overview of biofilm-specific resistance mechanisms is provided, but this is a highly multifactorial and rapidly expanding field that warrants further research. Progression in this field is dependent on the development of suitable biofilm models that acknowledge the complexity of the ocular environment. Abiotic models of biofilm formation (where biofilms are studied on non-living surfaces) currently dominate the literature, but co-culture infection models are beginning to emerge. In vitro, ex vivo and in vivo corneal infection models have now been reported which use a variety of different experimental techniques and animal models. In this review, we will discuss existing corneal infection models and their application in the study of biofilms and host-pathogen interactions at the corneal surface. |
format | Online Article Text |
id | pubmed-7696224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76962242020-11-29 Corneal Infection Models: Tools to Investigate the Role of Biofilms in Bacterial Keratitis Urwin, Lucy Okurowska, Katarzyna Crowther, Grace Roy, Sanhita Garg, Prashant Karunakaran, Esther MacNeil, Sheila Partridge, Lynda J. Green, Luke R. Monk, Peter N. Cells Review Bacterial keratitis is a corneal infection which may cause visual impairment or even loss of the infected eye. It remains a major cause of blindness in the developing world. Staphylococcus aureus and Pseudomonas aeruginosa are common causative agents and these bacterial species are known to colonise the corneal surface as biofilm populations. Biofilms are complex bacterial communities encased in an extracellular polymeric matrix and are notoriously difficult to eradicate once established. Biofilm bacteria exhibit different phenotypic characteristics from their planktonic counterparts, including an increased resistance to antibiotics and the host immune response. Therefore, understanding the role of biofilms will be essential in the development of new ophthalmic antimicrobials. A brief overview of biofilm-specific resistance mechanisms is provided, but this is a highly multifactorial and rapidly expanding field that warrants further research. Progression in this field is dependent on the development of suitable biofilm models that acknowledge the complexity of the ocular environment. Abiotic models of biofilm formation (where biofilms are studied on non-living surfaces) currently dominate the literature, but co-culture infection models are beginning to emerge. In vitro, ex vivo and in vivo corneal infection models have now been reported which use a variety of different experimental techniques and animal models. In this review, we will discuss existing corneal infection models and their application in the study of biofilms and host-pathogen interactions at the corneal surface. MDPI 2020-11-10 /pmc/articles/PMC7696224/ /pubmed/33182687 http://dx.doi.org/10.3390/cells9112450 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Urwin, Lucy Okurowska, Katarzyna Crowther, Grace Roy, Sanhita Garg, Prashant Karunakaran, Esther MacNeil, Sheila Partridge, Lynda J. Green, Luke R. Monk, Peter N. Corneal Infection Models: Tools to Investigate the Role of Biofilms in Bacterial Keratitis |
title | Corneal Infection Models: Tools to Investigate the Role of Biofilms in Bacterial Keratitis |
title_full | Corneal Infection Models: Tools to Investigate the Role of Biofilms in Bacterial Keratitis |
title_fullStr | Corneal Infection Models: Tools to Investigate the Role of Biofilms in Bacterial Keratitis |
title_full_unstemmed | Corneal Infection Models: Tools to Investigate the Role of Biofilms in Bacterial Keratitis |
title_short | Corneal Infection Models: Tools to Investigate the Role of Biofilms in Bacterial Keratitis |
title_sort | corneal infection models: tools to investigate the role of biofilms in bacterial keratitis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696224/ https://www.ncbi.nlm.nih.gov/pubmed/33182687 http://dx.doi.org/10.3390/cells9112450 |
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