Journal article
A coding polymorphism in matrix metalloproteinase 9 reduces risk of scarring sequelae of ocular Chlamydia trachomatisinfection
- Abstract:
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Background: Trachoma, an infectious disease of the conjunctiva caused by Chlamydia trachomatis, is an important global cause of blindness. A dysregulated extracellular matrix (ECM) proteolysis during the processes of tissue repair following infection and inflammation are thought to play a key role in the development of fibrotic sequelae of infection, which ultimately leads to blindness. Expression and activity of matrix metalloproteinase 9 (MMP-9), a major effector of ECM turnover, is up-regulated in the inflamed conjunctiva of trachoma subjects. Genetic variation within the MMP9 gene affects in vitro MMP9 expression levels, enzymatic activity and susceptibility to various inflammatory and fibrotic conditions.
Methods: We genotyped 651 case-control pairs from trachoma endemic villages in The Gambia for coding single nucleotide polymorphisms (SNPs) in the MMP9 gene using the high-throughput Sequenom® system. Single marker and haplotype conditional logistic regression (CLR) analysis for disease association was performed.
Results: The Q279R mutation located in exon 6 of MMP9 was found to be associated with lower risk for severe disease sequelae of ocular Chlamydia trachomatis infection. This mutation, which leads to a nonsynonymous amino-acid change within the active site of the enzyme may reduce MMP-9-induced degradation of the structural components of the ECM during inflammatory episodes in trachoma and its associated fibrosis.
Conclusion: This work supports the hypothesis that MMP-9 has a role in the pathogenesis of blinding trachoma.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 331.1KB, Terms of use)
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- Publisher copy:
- 10.1186/1471-2350-7-40
Authors
- Publisher:
- BioMed Central
- Journal:
- BMC Medical Genetics More from this journal
- Volume:
- 7
- Article number:
- 40
- Publication date:
- 2006-04-27
- Acceptance date:
- 2006-04-27
- DOI:
- EISSN:
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1471-2350
- Language:
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English
- Keywords:
- UUID:
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uuid:3489790a-2ae2-4815-9c9b-7008c841df65
- Local pid:
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pubs:40014
- Source identifiers:
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40014
- Deposit date:
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2012-12-19
Terms of use
- Copyright holder:
- Natividad et al
- Copyright date:
- 2006
- Notes:
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© 2006 Natividad et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
- Licence:
- CC Attribution (CC BY)
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