Pinnock Abigail, Shivshetty Nagaveni, Roy Sanhita, Rimmer Stephen, Douglas Ian, MacNeil Sheila, Garg Prashant
University of Sheffield, Sheffield, S10 2TA, UK.
LV Prasad Eye Institute, Banjara Hills, Hyderabad, 500034, India.
Graefes Arch Clin Exp Ophthalmol. 2017 Feb;255(2):333-342. doi: 10.1007/s00417-016-3546-0. Epub 2016 Nov 14.
In the study of microbial keratitis, in vivo animal models often require a large number of animals, and in vitro monolayer cell culture does not maintain the three-dimensional structure of the tissues or cell-to-cell communication of in vivo models. Here, we propose reproducible ex vivo models of single- and dual-infection keratitis as an alternative to in vivo and in vitro models.
Excised rabbit and human corneoscleral rims maintained in organ culture were infected using 10 cells of Staphylococcus aureus, Pseudomonas aeruginosa, Candida albicans or Fusarium solani. The infection was introduced by wounding with a scalpel and exposing corneas to the microbial suspension or by intrastromal injection. Post-inoculation, corneas were maintained for 24 and 48 h at 37 °C. After incubation, corneas were either homogenised to determine colony-forming units (CFU)/cornea or processed for histological examination using routine staining methods. Single- and mixed-species infections were compared.
We observed a significant increase in CFU after 48 h compared to 24 h with S. aureus and P. aeruginosa. However, no such increase was observed in corneas infected with C. albicans or F. solani. The injection method yielded an approximately two- to 100-fold increase (p < 0.05) in the majority of organisms from infected corneas. Histology of the scalpel-wounded and injection models indicated extensive infiltration of P. aeruginosa throughout the entire cornea, with less infiltration observed for S. aureus, C. albicans and F. solani. The models also supported dual infections.
Both scalpel wounding and injection methods are suitable for inducing infection of ex vivo rabbit and human cornea models. These simple and reproducible models will be useful as an alternative to in vitro and in vivo models for investigating the detection and treatment of microbial keratitis, particularly when this might be due to two infective organisms.
在微生物性角膜炎的研究中,体内动物模型通常需要大量动物,而体外单层细胞培养无法维持组织的三维结构或体内模型的细胞间通讯。在此,我们提出可重复的单感染和双感染角膜炎离体模型,作为体内和体外模型的替代方案。
将切除并维持在器官培养中的兔和人角膜缘用10个金黄色葡萄球菌、铜绿假单胞菌、白色念珠菌或茄病镰刀菌细胞进行感染。通过用手术刀划伤并将角膜暴露于微生物悬液或通过基质内注射来引入感染。接种后,将角膜在37℃下维持24和48小时。孵育后,将角膜匀浆以确定每角膜的菌落形成单位(CFU),或使用常规染色方法进行组织学检查。比较单菌种和混合菌种感染。
与24小时相比,我们观察到金黄色葡萄球菌和铜绿假单胞菌在48小时后CFU显著增加。然而,在感染白色念珠菌或茄病镰刀菌的角膜中未观察到这种增加。注射方法使大多数受感染角膜中的生物体数量增加了约2至100倍(p<0.05)。手术刀划伤和注射模型的组织学表明,铜绿假单胞菌在整个角膜中广泛浸润,而金黄色葡萄球菌、白色念珠菌和茄病镰刀菌的浸润较少。这些模型也支持双感染。
手术刀划伤和注射方法均适用于诱导离体兔和人角膜模型感染。这些简单且可重复的模型将作为体外和体内模型的替代方案,用于研究微生物性角膜炎的检测和治疗,特别是当可能由两种感染性生物体引起时。