4 research outputs found
Ex vivo rabbit and human corneas as models for bacterial and fungal keratitis.
PURPOSE: 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. METHODS: Excised rabbit and human corneoscleral rims maintained in organ culture were infected using 10(8) 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. RESULTS: 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. CONCLUSIONS: 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
Generation and use of functionalised hydrogels that can rapidly sample infected surfaces
This paper outlined our method for developing polymer-linked contact lens type materials for rapid detection and differentiation of Gram-positive, Gram-negative bacteria and fungi in infected corneas. It can be applied to both model synthetic or ex-vivo corneal models and has been successfully trialed in an initial efficacy tested animal study. First a hydrogel substrate for the swab material is selected, we have demonstrated selective swabs using a glycerol monomethacrylate hydrogel. Alternatively any commercial material with carboxylic acid functional groups is suitable but risks nonspecific adhesion. This is then functionalised via use of N-hydroxysuccinimide reaction with amine groups on the specified highly branched polymer ligand (either individually gram negative, gram positive or fungal binding polymers or a combination of all three can be employed for desired sensing application). The hydrogel is then cut into swabs suitable for sampling, used, and then the presence of gram positive, game negative and fungi are disclosed by the sequential addition of dyes (fluorescent vancomycin, fluorescein isothiocyanate and calcofluor white).
In summary this method presents:
Method to produce glycerol monomethacrylate hydrogels to minimize nonspecific binding
Methods of attaching pathogen binding highly branched polymers to produce selective hydrogel swabs
Method for disclosing bound pathogens to this swab using sequential dye additio
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Branched amphotericin functional poly(N-isopropyl acrylamide): an antifungal polymer
Branched poly(N-isopropylacrylamide) was functionalized with Amphotericin B (AmB) at the chain ends to produce an antifungal material. The polymer showed antifungal properties against AmB-sensitive strains of Candida albicans, Fusarium keratoplasticum and Aspergillus flavus (minimal inhibitory concentration ranged from 5 to 500 µg ml−1) but was not effective against an AmB resistant strain of C. albicans nor against Candida tropicalis. The polymer end groups bound to the AmB target, ergosterol, and the fluorescence spectrum of a dye used as a solvatochromic probe, Nile red, was blue shifted indicating that segments of the polymer became desolvated on binding. The polymer was less toxic to corneal and renal epithelial cells and explanted corneal tissue than the free drug. Also, the polymer did not induce reactive oxygen species release from peripheral blood mononuclear cells, nor did it cause a substantial release of the proinflammatory cytokines, tumour necrosis factor-α and interleukin-1β (at 0.5 mg ml−1)
Evaluation of ligand modified poly (N-Isopropyl acrylamide) hydrogel for etiological diagnosis of corneal infection
YesCorneal ulcers, a leading cause of blindness in the developing world are treated inappropriately without prior
microbiology assessment because of issues related to availability or cost of accessing these services.
In this work we aimed to develop a device for identifying the presence of Gram-positive or Gram-negative
bacteria or fungi that can be used by someone without the need for a microbiology laboratory. Working with
branched poly (N-isopropyl acrylamide) (PNIPAM) tagged with Vancomycin, Polymyxin B, or Amphotericin B to
bind Gram-positive bacteria, Gram-negative bacteria and fungi respectively, grafted onto a single hydrogel we
demonstrated specific binding of the organisms. The limit of detection of the microbes by these polymers was
between 10 and 4 organisms per high power field (100X) for bacteria and fungi binding polymers respectively.
Using ex vivo and animal cornea infection models infected with bacteria, fungi or both we than demonstrated
that the triple functionalised hydrogel could pick up all 3 organisms after being in place for 30 min. To confirm
the presence of bacteria and fungi we used conventional microbiology techniques and fluorescently labelled
ligands or dyes.
While we need to develop an easy-to-use either a colorimetric or an imaging system to detect the fluorescent
signals, this study presents for the first time a simple to use hydrogel system, which can be applied to infected
eyes and specifically binds different classes of infecting agents within a short space of time. Ultimately this
diagnostic system will not require trained microbiologists for its use and will be used at the point-of-care.We gratefully acknowledge support for this research by the Well- come Trust which provided funding for Shivshetty, Swift and Pinnock (Grant 0998800/B/12/Z).The full-text of this article will be released for public view at the end of the the publisher embargo on 3rd Dec 2022