一种新型低成本的眼内炎实验模型玻璃体内注射方法。

IF 1.6 Q3 OPHTHALMOLOGY
Dhanwini Rudraprasad, Jaishree Gandhi, Poonam Naik, Milind N Naik, Chenchu Naidu, Dilip Kumar Mishra, Joveeta Joseph
{"title":"一种新型低成本的眼内炎实验模型玻璃体内注射方法。","authors":"Dhanwini Rudraprasad,&nbsp;Jaishree Gandhi,&nbsp;Poonam Naik,&nbsp;Milind N Naik,&nbsp;Chenchu Naidu,&nbsp;Dilip Kumar Mishra,&nbsp;Joveeta Joseph","doi":"10.18502/jovr.v18i3.13775","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Animal models are necessary in understanding the pathogenesis of endophthalmitis and are also necessary to assist the development of new therapeutics for this sight-threatening ocular inflammation. Hamilton syringes are usually preferred to inject pathogens when performing experiments on test subjects, however, this method has technical and financial disadvantages. In this study, we report the findings and assess the related benefits of applying a novel low-cost intravitreal injection technique to initiate endophthalmitis in a mouse model while using the Eppendorf tip and a 26G needle.</p><p><strong>Methods: </strong>The 18-hr culture of clinical isolates of bacteria (<i>Staphylococcus aureus</i> and <i>Pseudomonas aeruginosa</i>) and fungus (<i>Aspergillus flavus</i> and <i>Candida albicans</i>) were resuspended to a final concentration of 10,000 colony forming units (CFU)/1 µL which were separately injected intravitreally into C57BL/6 mice (6-8 weeks) using a 0.1-2.5µL pipette attached to the modified Eppendorf tip with a 26G needle. The contralateral eye served as vehicle/uninjected control. Disease progression was determined by assessing the corneal haze, opacity, bacterial burden, and retinal histology of the eyes used in the model. Following euthanization, bacteria-infected mice were enucleated after 24 hr of the initial injection, and fungus-infected mice after 72 hr.</p><p><strong>Results: </strong>Of the 50 mice injected, the modified technique was successful in 48 mice. Two mice were excluded due to cataract formed by accidental injury to the lens. The experimental endophthalmitis mice model successfully mimicked the natural clinical course. Clinical assessment and histopathology confirmed the influx of inflammatory cells into the posterior segment of the eye along with dissolution of retinal architecture.</p><p><strong>Conclusion: </strong>Our novel method of injection using a modified Eppendorf tip and 26G needle yielded a cost-effective mouse model of clinical endophthalmitis, resulting in reproducible infection for understanding various aspects of its pathobiology.</p>","PeriodicalId":16586,"journal":{"name":"Journal of Ophthalmic & Vision Research","volume":"18 3","pages":"272-282"},"PeriodicalIF":1.6000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432928/pdf/","citationCount":"1","resultStr":"{\"title\":\"A Novel and Low-cost Approach for Intravitreal Injection in an Experimental Model of Endophthalmitis.\",\"authors\":\"Dhanwini Rudraprasad,&nbsp;Jaishree Gandhi,&nbsp;Poonam Naik,&nbsp;Milind N Naik,&nbsp;Chenchu Naidu,&nbsp;Dilip Kumar Mishra,&nbsp;Joveeta Joseph\",\"doi\":\"10.18502/jovr.v18i3.13775\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Animal models are necessary in understanding the pathogenesis of endophthalmitis and are also necessary to assist the development of new therapeutics for this sight-threatening ocular inflammation. Hamilton syringes are usually preferred to inject pathogens when performing experiments on test subjects, however, this method has technical and financial disadvantages. In this study, we report the findings and assess the related benefits of applying a novel low-cost intravitreal injection technique to initiate endophthalmitis in a mouse model while using the Eppendorf tip and a 26G needle.</p><p><strong>Methods: </strong>The 18-hr culture of clinical isolates of bacteria (<i>Staphylococcus aureus</i> and <i>Pseudomonas aeruginosa</i>) and fungus (<i>Aspergillus flavus</i> and <i>Candida albicans</i>) were resuspended to a final concentration of 10,000 colony forming units (CFU)/1 µL which were separately injected intravitreally into C57BL/6 mice (6-8 weeks) using a 0.1-2.5µL pipette attached to the modified Eppendorf tip with a 26G needle. The contralateral eye served as vehicle/uninjected control. Disease progression was determined by assessing the corneal haze, opacity, bacterial burden, and retinal histology of the eyes used in the model. Following euthanization, bacteria-infected mice were enucleated after 24 hr of the initial injection, and fungus-infected mice after 72 hr.</p><p><strong>Results: </strong>Of the 50 mice injected, the modified technique was successful in 48 mice. Two mice were excluded due to cataract formed by accidental injury to the lens. The experimental endophthalmitis mice model successfully mimicked the natural clinical course. Clinical assessment and histopathology confirmed the influx of inflammatory cells into the posterior segment of the eye along with dissolution of retinal architecture.</p><p><strong>Conclusion: </strong>Our novel method of injection using a modified Eppendorf tip and 26G needle yielded a cost-effective mouse model of clinical endophthalmitis, resulting in reproducible infection for understanding various aspects of its pathobiology.</p>\",\"PeriodicalId\":16586,\"journal\":{\"name\":\"Journal of Ophthalmic & Vision Research\",\"volume\":\"18 3\",\"pages\":\"272-282\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2023-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432928/pdf/\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Ophthalmic & Vision Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.18502/jovr.v18i3.13775\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"OPHTHALMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Ophthalmic & Vision Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18502/jovr.v18i3.13775","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 1

摘要

目的:建立动物模型是了解眼内炎发病机制的必要条件,也是开发这种威胁视力的眼部炎症的新疗法的必要条件。在对测试对象进行实验时,通常首选汉密尔顿注射器注射病原体,然而,这种方法具有技术和经济上的缺点。在这项研究中,我们报告了研究结果,并评估了使用Eppendorf针尖和26G针在小鼠模型中应用一种新型低成本玻璃体内注射技术引发眼内炎的相关益处。方法:将临床分离的细菌(金黄色葡萄球菌和铜绿假单胞菌)和真菌(黄曲霉和白色念珠菌)重悬至终浓度为10000菌落形成单位(CFU)/1µL,分别用0.1 ~ 2.5µL移液管连接改良的埃本多夫针尖,用26G针通过玻璃体注射到C57BL/6小鼠体内(6 ~ 8周)。对侧眼作为载体/未注射对照。通过评估模型中使用的眼睛的角膜薄雾、混浊、细菌负担和视网膜组织学来确定疾病进展。安乐死后,细菌感染的小鼠在初始注射24小时后去核,真菌感染的小鼠在72小时后去核。结果:50只小鼠注射后,改良技术成功48只。2只小鼠因晶状体意外损伤形成白内障而被排除。实验小鼠眼内炎模型成功地模拟了眼内炎的自然临床过程。临床评估和组织病理学证实炎症细胞涌入眼球后段,同时视网膜结构溶解。结论:我们使用改良的Eppendorf针尖和26G针的新型注射方法产生了一种具有成本效益的临床眼内炎小鼠模型,导致可重复感染,从而了解其病理生物学的各个方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Novel and Low-cost Approach for Intravitreal Injection in an Experimental Model of Endophthalmitis.

A Novel and Low-cost Approach for Intravitreal Injection in an Experimental Model of Endophthalmitis.

A Novel and Low-cost Approach for Intravitreal Injection in an Experimental Model of Endophthalmitis.

A Novel and Low-cost Approach for Intravitreal Injection in an Experimental Model of Endophthalmitis.

Purpose: Animal models are necessary in understanding the pathogenesis of endophthalmitis and are also necessary to assist the development of new therapeutics for this sight-threatening ocular inflammation. Hamilton syringes are usually preferred to inject pathogens when performing experiments on test subjects, however, this method has technical and financial disadvantages. In this study, we report the findings and assess the related benefits of applying a novel low-cost intravitreal injection technique to initiate endophthalmitis in a mouse model while using the Eppendorf tip and a 26G needle.

Methods: The 18-hr culture of clinical isolates of bacteria (Staphylococcus aureus and Pseudomonas aeruginosa) and fungus (Aspergillus flavus and Candida albicans) were resuspended to a final concentration of 10,000 colony forming units (CFU)/1 µL which were separately injected intravitreally into C57BL/6 mice (6-8 weeks) using a 0.1-2.5µL pipette attached to the modified Eppendorf tip with a 26G needle. The contralateral eye served as vehicle/uninjected control. Disease progression was determined by assessing the corneal haze, opacity, bacterial burden, and retinal histology of the eyes used in the model. Following euthanization, bacteria-infected mice were enucleated after 24 hr of the initial injection, and fungus-infected mice after 72 hr.

Results: Of the 50 mice injected, the modified technique was successful in 48 mice. Two mice were excluded due to cataract formed by accidental injury to the lens. The experimental endophthalmitis mice model successfully mimicked the natural clinical course. Clinical assessment and histopathology confirmed the influx of inflammatory cells into the posterior segment of the eye along with dissolution of retinal architecture.

Conclusion: Our novel method of injection using a modified Eppendorf tip and 26G needle yielded a cost-effective mouse model of clinical endophthalmitis, resulting in reproducible infection for understanding various aspects of its pathobiology.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
3.60
自引率
0.00%
发文量
63
审稿时长
30 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信