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Association between Moraxella keratitis and advanced glycation end products
Hidenori Inoue1, Koji Toriyama2, Naoko Takahira2
1Department of Ophthalmology, Ehime University Graduate School of Medicine, Shitsukawa, Toon, Ehime, 791-0295, Japan. inoue.hidenori.yo@ehime-u.ac.jp.
Abstract:
Diabetes mellitus is recognized as a major predisposing factor for Moraxella keratitis. However, how diabetes mellitus contributes to Moraxella keratitis remains unclear. In this study, we examined Moraxella keratitis; based on the findings, we investigated the impact of advanced glycation end products (AGEs) deposition in the cornea of individuals with diabetic mellitus on the adhesion of Moraxella isolates to the cornea. A retrospective analysis of 27 culture-proven cases of Moraxella keratitis at Ehime University Hospital (March 2006 to February 2022) was performed. Moraxella isolates were identified using matrix-assisted laser desorption ionization time-of-flight mass spectrometry. Among the patients, 30.4% had diabetes mellitus and 22.2% had the predominant ocular condition of using steroid eye drops. The species identified were Moraxella nonliquefaciens in 59.3% and Moraxella lacunata in 40.7% of patients. To investigate the underlying mechanisms, we assessed the effects of M. nonliquefaciens adherence to simian virus 40-immortalized human corneal epithelial cells (HCECs) with or without AGEs. The results demonstrated the number of M. nonliquefaciens adhering to HCECs was significantly increased by adding AGEs compared with that in controls (p < 0.01). Furthermore, in the corneas of streptozotocin-induced diabetic C57BL/6 mice treated with or without pyridoxamine, an AGE inhibitor, the number of M. nonliquefaciens adhering to the corneas of diabetic mice was significantly reduced by pyridoxamine treatment (p < 0.05). In conclusion, the development of Moraxella keratitis may be significantly influenced by the deposition of AGEs on the corneal epithelium of patients with diabetes mellitus.
Insights
Diabetes mellitus increases Moraxella keratitis risk. Advanced glycation end products (AGEs) in the cornea enhance Moraxella bacterial adhesion, suggesting AGEs contribute to this serious eye infection in diabetic patients.
Area of Science:
- Ophthalmology
- Microbiology
- Endocrinology
Background:
- Diabetes mellitus is a known risk factor for Moraxella keratitis.
- The precise mechanisms linking diabetes to Moraxella keratitis are not fully understood.
- Advanced glycation end products (AGEs) accumulate in diabetic tissues.
Purpose of the Study:
- To investigate the impact of advanced glycation end products (AGEs) deposition in the cornea on Moraxella bacterial adhesion.
- To explore the role of AGEs in the pathogenesis of Moraxella keratitis in diabetic patients.
Main Methods:
- Retrospective analysis of 27 culture-proven Moraxella keratitis cases.
- Identification of Moraxella isolates using MALDI-TOF mass spectrometry.
- In vitro assessment of Moraxella nonliquefaciens adherence to human corneal epithelial cells (HCECs) with and without AGEs.
- In vivo study using streptozotocin-induced diabetic mice treated with an AGE inhibitor.
Main Results:
- 30.4% of patients with Moraxella keratitis had diabetes mellitus.
- Moraxella nonliquefaciens adherence to HCECs significantly increased with AGEs.
- Pyridoxamine treatment significantly reduced Moraxella nonliquefaciens adherence in diabetic mouse corneas.
Conclusions:
- AGEs deposition in the corneal epithelium may significantly influence the development of Moraxella keratitis.
- Targeting AGEs could be a potential therapeutic strategy for Moraxella keratitis in diabetic individuals.
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