Evidence map›Paper›PMID 28275313›Full record

ArticleMolecular vision2017

Zinc oxide tetrapods inhibit herpes simplex virus infection of cultured corneas.

Neil Duggal, Dinesh Jaishankar, Tejabhiram Yadavalli, Satvik Hadigal, Yogendra Kumar Mishra, Rainer Adelung, Deepak Shukla

Abstract read
In one paragraph

Article in Molecular vision, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. 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.

Neil DuggalDepartment of Ophthalmology and Visual Sciences, University of Illinois at Chicago, IL.
Dinesh JaishankarDepartment of Ophthalmology and Visual Sciences, University of Illinois at Chicago, IL; Department of Bioengineering, University of Illinois at Chicago, IL.
Tejabhiram YadavalliDepartment of Ophthalmology and Visual Sciences, University of Illinois at Chicago, IL.
Satvik HadigalDepartment of Ophthalmology and Visual Sciences, University of Illinois at Chicago, IL.
Yogendra Kumar MishraFunctional Nanomaterials, Institute for Materials Science, Kiel University, Kiel, Germany.
Rainer AdelungFunctional Nanomaterials, Institute for Materials Science, Kiel University, Kiel, Germany.
Deepak ShuklaDepartment of Ophthalmology and Visual Sciences, University of Illinois at Chicago, IL; Department of Bioengineering, University of Illinois at Chicago, IL; Department of Microbiology and Immunology, University of Illinois at Chicago, IL.

Funding

Translational Core for Therapeutic and Diagnostic DevelopmentP30EY001792 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI AAKALU, VINAY · 1985 to 2025
$14.8M
A new molecular therapy against ocular herpesR01EY024710 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DEEPAK SHUKLA · 2015 to 2026
$5.2M
NEI NIH HHS P30 EY001792NEI NIH HHS R01 EY024710
6 · The paper itself

Abstract

purposeInfection of the human cornea by herpes simplex virus type-1 (HSV-1) can cause significant vision loss. The purpose of this study was to develop an ex vivo model to visualize viral growth and spread in the cornea. The model was also used to analyze cytokine production and study the antiviral effects of zinc oxide tetrapods.

methodsA β-galactosidase-expressing recombinant virus, HSV-1(KOS)tk12, was used to demonstrate the ability of the virus to enter and develop blue plaques on human corneal epithelial (HCE) cells and corneal tissues. Freshly obtained porcine corneas were cultured and then scratched before infection with HSV-1(KOS)tk12. The blue plaques on the corneas were imaged using a stereomicroscope. Western blot analysis for HSV-1 proteins was performed to verify HSV-1 infection of the cornea. Using the ex vivo model, zinc oxide tetrapods were tested for their anti-HSV-1 potential, and a cytokine profile was developed to assess the effects of the treatment.

resultsCultured corneas and the use of β-galactosidase-expressing HSV-1(KOS)tk12 virus can provide an attractive ex vivo model to visualize and study HSV-1 entry and spread of the infection in tissues. We found that unlike cultured HCE cells, which demonstrated nearly 100% infectivity, HSV-1 infection of the cultured cornea was more restrictive and took longer to develop. We also found that the zinc oxide tetrapod-shaped nano- and microstructures inhibited HSV infection of the cultured cells, as well as the cultured corneas. The cytokine profile of the infected samples was consistent with previous studies of HSV-1 corneal infection.

conclusionsThe ability to visualize HSV-1 growth and spread in corneal tissues can provide new details about HSV-1 infection of the cornea and the efficacy of new cornea-specific antiviral drug candidates. The ex vivo model also demonstrates antiviral effects of zinc oxide tetrapods and adequately portrays the drug delivery issues that cornea-specific treatments face.

Indexed as

AnimalsCells, CulturedCorneaCytokinesEpithelial CellsEpithelium, CornealHerpes SimplexHerpesvirus 1, HumanHumansImmunity, InnateSus scrofaThymidine KinaseVirus InternalizationZinc OxideCytokinesThymidine KinaseZinc Oxide

Identifiers

PMID28275313
PMCPMC5334001

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.