The protective effect of URP20 on ocular Staphylococcus aureus and Escherichia coli infection in rats

Abstract Background Infectious keratitis, a medical emergency with acute and rapid disease progression may lead to severe visual impairment and even blindness. Herein, an antimicrobial polypeptide from Crassostrea hongkongensis, named URP20, was evaluated for its therapeutic efficacy against keratit...

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Main Authors: Meng Li, Danli Xin, Jian Gao, Quanyong Yi, Jianshu Yuan, Yongbo Bao, Yan Gong
Format: Article
Language:English
Published: BMC 2022-12-01
Series:BMC Ophthalmology
Subjects:
Online Access:https://doi.org/10.1186/s12886-022-02752-w
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author Meng Li
Danli Xin
Jian Gao
Quanyong Yi
Jianshu Yuan
Yongbo Bao
Yan Gong
author_facet Meng Li
Danli Xin
Jian Gao
Quanyong Yi
Jianshu Yuan
Yongbo Bao
Yan Gong
author_sort Meng Li
collection DOAJ
description Abstract Background Infectious keratitis, a medical emergency with acute and rapid disease progression may lead to severe visual impairment and even blindness. Herein, an antimicrobial polypeptide from Crassostrea hongkongensis, named URP20, was evaluated for its therapeutic efficacy against keratitis caused by Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) infection in rats, respectively. Methods A needle was used to scratch the surface of the eyeballs of rats and infect them with S. aureus and E.coli to construct a keratitis model. The two models were treated by giving 100 μL 100 μM URP20 drops. Positive drugs for S. aureus and E. coli infection were cefazolin eye drops and tobramycin eye drops, respectively. For the curative effect, the formation of blood vessels in the fundus was observed by a slit lamp (the third day). At the end of the experiment, the condition of the injured eye was photographed by cobalt blue light using 5 μL of 1% sodium fluorescein. The pathological damage to corneal tissues was assessed using hematoxylin–eosin staining, and the expression level of vascular endothelial growth factor (VEGF) was detected by immunohistochemistry. Results URP20 alleviated the symptoms of corneal neovascularization as observed by slit lamp and cobalt blue lamp. The activity of S. aureus and E.coli is inhibited by URP20 to protect corneal epithelial cells and reduce corneal stromal bacterial invasion. It also prevented corneal thickening and inhibited neovascularization by reducing VEGF expression at the cornea. Conclusion URP20 can effectively inhibit keratitis caused by E.coli as well as S. aureus in rats, as reflected by the inhibition of corneal neovascularization and the reduction in bacterial damage to the cornea.
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spelling doaj.art-bd664a51e4bc4e7080dbced4604187fc2023-01-01T12:15:32ZengBMCBMC Ophthalmology1471-24152022-12-0122111010.1186/s12886-022-02752-wThe protective effect of URP20 on ocular Staphylococcus aureus and Escherichia coli infection in ratsMeng Li0Danli Xin1Jian Gao2Quanyong Yi3Jianshu Yuan4Yongbo Bao5Yan Gong6School of Medicine, Ningbo UniversityDepartment of Ophtalmology, Ningbo Eye HospitalDepartment of Ophtalmology, Ningbo Eye HospitalDepartment of Ophtalmology, Ningbo Eye HospitalDepartment of Ophtalmology, Ningbo Eye HospitalCollege of Biological & Environmental Sciences, Zhejiang Wanli UniversityDepartment of Ophtalmology, Ningbo Eye HospitalAbstract Background Infectious keratitis, a medical emergency with acute and rapid disease progression may lead to severe visual impairment and even blindness. Herein, an antimicrobial polypeptide from Crassostrea hongkongensis, named URP20, was evaluated for its therapeutic efficacy against keratitis caused by Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) infection in rats, respectively. Methods A needle was used to scratch the surface of the eyeballs of rats and infect them with S. aureus and E.coli to construct a keratitis model. The two models were treated by giving 100 μL 100 μM URP20 drops. Positive drugs for S. aureus and E. coli infection were cefazolin eye drops and tobramycin eye drops, respectively. For the curative effect, the formation of blood vessels in the fundus was observed by a slit lamp (the third day). At the end of the experiment, the condition of the injured eye was photographed by cobalt blue light using 5 μL of 1% sodium fluorescein. The pathological damage to corneal tissues was assessed using hematoxylin–eosin staining, and the expression level of vascular endothelial growth factor (VEGF) was detected by immunohistochemistry. Results URP20 alleviated the symptoms of corneal neovascularization as observed by slit lamp and cobalt blue lamp. The activity of S. aureus and E.coli is inhibited by URP20 to protect corneal epithelial cells and reduce corneal stromal bacterial invasion. It also prevented corneal thickening and inhibited neovascularization by reducing VEGF expression at the cornea. Conclusion URP20 can effectively inhibit keratitis caused by E.coli as well as S. aureus in rats, as reflected by the inhibition of corneal neovascularization and the reduction in bacterial damage to the cornea.https://doi.org/10.1186/s12886-022-02752-wURP20Infectious keratitisAntimicrobial polypeptideOcular infectionCrassostrea hongkongensis
spellingShingle Meng Li
Danli Xin
Jian Gao
Quanyong Yi
Jianshu Yuan
Yongbo Bao
Yan Gong
The protective effect of URP20 on ocular Staphylococcus aureus and Escherichia coli infection in rats
BMC Ophthalmology
URP20
Infectious keratitis
Antimicrobial polypeptide
Ocular infection
Crassostrea hongkongensis
title The protective effect of URP20 on ocular Staphylococcus aureus and Escherichia coli infection in rats
title_full The protective effect of URP20 on ocular Staphylococcus aureus and Escherichia coli infection in rats
title_fullStr The protective effect of URP20 on ocular Staphylococcus aureus and Escherichia coli infection in rats
title_full_unstemmed The protective effect of URP20 on ocular Staphylococcus aureus and Escherichia coli infection in rats
title_short The protective effect of URP20 on ocular Staphylococcus aureus and Escherichia coli infection in rats
title_sort protective effect of urp20 on ocular staphylococcus aureus and escherichia coli infection in rats
topic URP20
Infectious keratitis
Antimicrobial polypeptide
Ocular infection
Crassostrea hongkongensis
url https://doi.org/10.1186/s12886-022-02752-w
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