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miRNAs that associate with conjunctival inflammation and ocular Chlamydia trachomatis infection do not predict progressive disease
We previously showed that conjunctival miR-147b and miR-1285 were upregulated in Gambian adults with inflammatory scarring trachoma, and miR-155 and miR-184 expression was strongly associated with conjunctival inflammation and ocular Chlamydia trachomatis infection in children from Guinea-Bissau. We...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399916/ https://www.ncbi.nlm.nih.gov/pubmed/28175294 http://dx.doi.org/10.1093/femspd/ftx016 |
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author | Derrick, Tamsyn Ramadhani, Athumani M. Mtengai, Karim Massae, Patrick Burton, Matthew J. Holland, Martin J. |
author_facet | Derrick, Tamsyn Ramadhani, Athumani M. Mtengai, Karim Massae, Patrick Burton, Matthew J. Holland, Martin J. |
author_sort | Derrick, Tamsyn |
collection | PubMed |
description | We previously showed that conjunctival miR-147b and miR-1285 were upregulated in Gambian adults with inflammatory scarring trachoma, and miR-155 and miR-184 expression was strongly associated with conjunctival inflammation and ocular Chlamydia trachomatis infection in children from Guinea-Bissau. We investigated whether the single or combined expression of miR-147b, miR-1285, miR-155 and miR-184 was able to identify individuals with increased risk of incident or progressive scarring trachoma. Conjunctival swab samples were collected from 506 children between the ages of 4 and 12 living in northern Tanzania. These 506 samples formed the baseline sample set of a 4-year longitudinal study. Chlamydia trachomatis infection was diagnosed by droplet digital PCR and expression of miR-155, miR-184, miR-1285 and miR-147b was tested by qPCR. Individuals were assessed for incidence and progression of conjunctival scarring by comparison of conjunctival photographs taken at baseline and 4 years later. miR-184 and miR-155 were strongly associated with inflammation and infection at baseline; however, no miR was associated with 4-year scarring incidence or progression. miR-184 expression was more strongly downregulated during inflammation in non-progressors relative to progressors, suggesting that a disequilibrium in the efficiency of wound healing is a significant determinant of progressive conjunctival fibrosis. |
format | Online Article Text |
id | pubmed-5399916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53999162017-04-28 miRNAs that associate with conjunctival inflammation and ocular Chlamydia trachomatis infection do not predict progressive disease Derrick, Tamsyn Ramadhani, Athumani M. Mtengai, Karim Massae, Patrick Burton, Matthew J. Holland, Martin J. Pathog Dis Research Article We previously showed that conjunctival miR-147b and miR-1285 were upregulated in Gambian adults with inflammatory scarring trachoma, and miR-155 and miR-184 expression was strongly associated with conjunctival inflammation and ocular Chlamydia trachomatis infection in children from Guinea-Bissau. We investigated whether the single or combined expression of miR-147b, miR-1285, miR-155 and miR-184 was able to identify individuals with increased risk of incident or progressive scarring trachoma. Conjunctival swab samples were collected from 506 children between the ages of 4 and 12 living in northern Tanzania. These 506 samples formed the baseline sample set of a 4-year longitudinal study. Chlamydia trachomatis infection was diagnosed by droplet digital PCR and expression of miR-155, miR-184, miR-1285 and miR-147b was tested by qPCR. Individuals were assessed for incidence and progression of conjunctival scarring by comparison of conjunctival photographs taken at baseline and 4 years later. miR-184 and miR-155 were strongly associated with inflammation and infection at baseline; however, no miR was associated with 4-year scarring incidence or progression. miR-184 expression was more strongly downregulated during inflammation in non-progressors relative to progressors, suggesting that a disequilibrium in the efficiency of wound healing is a significant determinant of progressive conjunctival fibrosis. Oxford University Press 2017-02-08 2017-03 /pmc/articles/PMC5399916/ /pubmed/28175294 http://dx.doi.org/10.1093/femspd/ftx016 Text en © FEMS 2017. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Derrick, Tamsyn Ramadhani, Athumani M. Mtengai, Karim Massae, Patrick Burton, Matthew J. Holland, Martin J. miRNAs that associate with conjunctival inflammation and ocular Chlamydia trachomatis infection do not predict progressive disease |
title | miRNAs that associate with conjunctival inflammation and ocular Chlamydia trachomatis infection do not predict progressive disease |
title_full | miRNAs that associate with conjunctival inflammation and ocular Chlamydia trachomatis infection do not predict progressive disease |
title_fullStr | miRNAs that associate with conjunctival inflammation and ocular Chlamydia trachomatis infection do not predict progressive disease |
title_full_unstemmed | miRNAs that associate with conjunctival inflammation and ocular Chlamydia trachomatis infection do not predict progressive disease |
title_short | miRNAs that associate with conjunctival inflammation and ocular Chlamydia trachomatis infection do not predict progressive disease |
title_sort | mirnas that associate with conjunctival inflammation and ocular chlamydia trachomatis infection do not predict progressive disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399916/ https://www.ncbi.nlm.nih.gov/pubmed/28175294 http://dx.doi.org/10.1093/femspd/ftx016 |
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