Evidence map›Paper›PMID 27844206›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2017

Ex vivo rabbit and human corneas as models for bacterial and fungal keratitis.

Abigail Pinnock, Nagaveni Shivshetty, Sanhita Roy, Stephen Rimmer, Ian Douglas, Sheila MacNeil, Prashant Garg

Open access · hybridAbstract read
In one paragraph

Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.3field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Ultrastructural polymicrobialFuture microbiology · 2025
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  3. Exploring interspecies differences inJournal of medical microbiology · 2024
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  5. Concanavalin A Delivers a Photoactive Protein to the Bacterial Wall.International journal of molecular sciences · 2024
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  6. Article
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  9. Article
  10. How to study biofilms: technological advancements in clinical biofilm research.Frontiers in cellular and infection microbiology · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Genipin in an Ex Vivo Corneal Model of Bacterial and Fungal Keratitis.Translational vision science & technology · 2021
    Article
  16. Article
  17. Review
  18. Key Role of Staphylococcal Fibronectin-Binding Proteins During the Initial Stage ofFrontiers in cellular and infection microbiology · 2021
    Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Abigail PinnockUniversity of Sheffield, Sheffield, S10 2TA, UK.
Nagaveni ShivshettyLV Prasad Eye Institute, Banjara Hills, Hyderabad, 500034, India.
Sanhita RoyLV Prasad Eye Institute, Banjara Hills, Hyderabad, 500034, India.
Stephen RimmerUniversity of Bradford, Bradford, BD7 1DP, UK.
Ian DouglasUniversity of Sheffield, Sheffield, S10 2TA, UK.
Sheila MacNeilUniversity of Sheffield, Sheffield, S10 2TA, UK. s.macneil@sheffield.ac.uk.
Prashant GargLV Prasad Eye Institute, Banjara Hills, Hyderabad, 500034, India.
L V Prasad Eye Institute · INUniversity of Sheffield · GBUniversity of Bradford · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

purposeIn 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.

methodsExcised rabbit and human corneoscleral rims maintained in organ culture were infected using 10

resultsWe 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.

conclusionsBoth 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.

Indexed as

AnimalsBacteriaColony Count, MicrobialCorneaDisease Models, AnimalEye Infections, BacterialEye Infections, FungalFungiHumansKeratitisMicroscopy, FluorescenceOrgan Culture TechniquesRabbitsColony-forming unitsCorneal modelEx vivo corneaMicrobial keratitis

Identifiers

PMID27844206
PMCPMC5285415
OpenAlexW2551369376

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.