Evidence map›Paper›PMID 34569661›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2021

Nerve-associated transient receptor potential ion channels can contribute to intrinsic resistance to bacterial adhesion in vivo.

Stephanie J Wan, Ananya Datta, Orneika Flandrin, Matteo M E Metruccio, Sophia Ma, Vincent Nieto, Abby R Kroken, Rose Z Hill, Diana M Bautista, David J Evans and 1 more

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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  11. Review
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

11 authors at 1 institution in 1 country.

Stephanie J WanVision Science Program, University of California, Berkeley, California, USA.
Ananya DattaSchool of Optometry, University of California, Berkeley, California, USA.
Orneika FlandrinVision Science Program, University of California, Berkeley, California, USA.
Matteo M E MetruccioSchool of Optometry, University of California, Berkeley, California, USA.
Sophia MaSchool of Optometry, University of California, Berkeley, California, USA.
Vincent NietoSchool of Optometry, University of California, Berkeley, California, USA.
Abby R KrokenSchool of Optometry, University of California, Berkeley, California, USA.
Rose Z HillDepartment of Molecular and Cell Biology and Helen Wills Neuroscience Institute, University of California, Berkeley, California, USA.
Diana M BautistaDepartment of Molecular and Cell Biology and Helen Wills Neuroscience Institute, University of California, Berkeley, California, USA.
David J EvansSchool of Optometry, University of California, Berkeley, California, USA.
Suzanne M J FleiszigVision Science Program, University of California, Berkeley, California, USA.
University of California, Berkeley · US

Funding

SIGNIFICANCE OF CORNEAL CELL INVASION BY BACTERIAR01EY011221 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI Suzanne MJ FLEISZIG · 1995 to 2026
$8.4M
Transient Receptor Potential Ion Channels and Corneal Defense Against Bacterial AdhesionR01EY030350 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI Suzanne MJ FLEISZIG · 2019 to 2026
$3.0M
NEI NIH HHS R01 EY011221NEI NIH HHS R01 EY030350
6 · The paper itself

Abstract

The cornea of the eye differs from other mucosal surfaces in that it lacks a viable bacterial microbiome and by its unusually high density of sensory nerve endings. Here, we explored the role of corneal nerves in preventing bacterial adhesion. Pharmacological and genetic methods were used to inhibit the function of corneal sensory nerves or their associated transient receptor potential cation channels TRPA1 and TRPV1. Impacts on bacterial adhesion, resident immune cells, and epithelial integrity were examined using fluorescent labeling and quantitative confocal imaging. TRPA1/TRPV1 double gene-knockout mice were more susceptible to adhesion of environmental bacteria and to that of deliberately-inoculated Pseudomonas aeruginosa. Supporting the involvement of TRPA1/TRPV1-expressing corneal nerves, P. aeruginosa adhesion was also promoted by treatment with bupivacaine, or ablation of TRPA1/TRPV1-expressing nerves using RTX. Moreover, TRPA1/TRPV1-dependent defense was abolished by enucleation which severs corneal nerves. High-resolution imaging showed normal corneal ultrastructure and surface-labeling by wheat-germ agglutinin for TRPA1/TRPV1 knockout murine corneas, and intact barrier function by absence of fluorescein staining. P. aeruginosa adhering to corneas after perturbation of nerve or TRPA1/TRPV1 function failed to penetrate the surface. Single gene-knockout mice showed roles for both TRPA1 and TRPV1, with TRPA1

Indexed as

Bacterial AdhesionCorneaAnimalsFemaleMaleMiceMice, KnockoutPseudomonas aeruginosaTRPA1 Cation ChannelTRPV Cation ChannelsTRPA1 Cation ChannelTrpa1 protein, mouseTRPV1 protein, mouseTRPV Cation Channelsbacterial adhesioncorneaepithelial defensesensory nervesTRP ion channels

Identifiers

PMID34569661
PMCPMC8486357
OpenAlexW3204825146

What OpenQuestion holds

Textmetadata
LicenceTDM
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.