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Analysis of the Epithelial Damage Produced by Entamoeba histolytica Infection
Published on: June 12, 2014
Mannose induces the release of cytopathic factors from Acanthamoeba castellanii
H Leher1, R Silvany, H Alizadeh
1Department of Ophthalmology, University of Texas Southwestern Medical Center, Dallas 75235-9057, USA.
Abstract:
Acanthamoeba keratitis is a chronic inflammatory disease of the cornea which is highly resistant to many antimicrobial agents. The pathogenic mechanisms of this disease are poorly understood. However, it is believed that the initial phases in the pathogenesis of Acanthamoeba keratitis involve parasite binding and lysis of the corneal epithelium. These processes were examined in vitro, using Acanthamoeba castellanii trophozoites. Parasites readily adhered to Chinese hamster corneal epithelial cells in vitro; however, parasite binding was strongly inhibited by mannose but not by lactose. Although mannose prevented trophozoite binding, it did not affect cytolysis of corneal epithelial cells. Moreover, mannose treatment induced trophozoites to release cytolytic factors that lysed corneal epithelial cells in vitro. These factors were uniquely induced by mannose because supernatants collected from either untreated trophozoites or trophozoites treated with other sugars failed to lyse corneal cells. The soluble factors were size fractionated in centrifugal concentrators and found to be > or = 100 kDa. Treatment of the supernatants with the serine protease inhibitor phenylmethylsulfonyl fluoride inhibited most, but not all, of the cytopathic activity. These data suggest that the binding of Acanthamoeba to mannosylated proteins on the corneal epithelium may exacerbate the pathogenic cascade by initiating the release of cytolytic factors.
Insights
Mannose binding to Acanthamoeba castellanii trophozoites surprisingly triggers the release of cytolytic factors, exacerbating corneal epithelial cell damage in Acanthamoeba keratitis.
Area of Science:
- Ophthalmology
- Microbiology
- Cell Biology
Background:
- Acanthamoeba keratitis is a severe corneal disease with poorly understood pathogenesis.
- It is characterized by resistance to antimicrobial treatments.
- Initial disease stages likely involve parasite adhesion and corneal epithelial cell lysis.
Purpose of the Study:
- To investigate the mechanisms of Acanthamoeba binding to corneal epithelial cells.
- To determine the role of specific sugars in parasite-host cell interactions.
- To identify factors involved in Acanthamoeba-induced corneal cell damage.
Main Methods:
- In vitro study using Acanthamoeba castellanii trophozoites and Chinese hamster corneal epithelial cells.
- Assessment of parasite adhesion inhibition by mannose and lactose.
- Analysis of cytolytic factor release and characterization using size fractionation and protease inhibition.
Main Results:
- Mannose significantly inhibited Acanthamoeba binding to corneal epithelial cells.
- Mannose treatment induced trophozoites to release soluble cytolytic factors (> or = 100 kDa).
- Serine protease inhibitors partially blocked the cytopathic activity of these released factors.
Conclusions:
- Mannose-mediated binding may trigger Acanthamoeba to release damaging cytolytic factors.
- This interaction could exacerbate the pathogenesis of Acanthamoeba keratitis.
- Understanding these mechanisms offers potential therapeutic targets.
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