Evidence map›Paper›PMID 25392356›Full record

ArticleJournal of clinical microbiology2015

Development of an immunochromatographic assay kit using fluorescent silica nanoparticles for rapid diagnosis of Acanthamoeba keratitis.

Koji Toriyama, Takashi Suzuki, Tomoyuki Inoue, Hiroshi Eguchi, Saichi Hoshi, Yoshitsugu Inoue, Hideki Aizawa, Kazutomi Miyoshi, Michio Ohkubo, Eiji Hiwatashi and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 22 citations in OpenAlex.

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

12 authors at 7 institutions in 1 country.

Koji ToriyamaDepartment of Ophthalmology, Ehime University, Graduate School of Medicine, Ehime, Japan.
Takashi SuzukiDepartment of Ophthalmology, Ehime University, Graduate School of Medicine, Ehime, Japan t-suzuki@m.ehime-u.ac.jp.
Tomoyuki InoueDepartment of Ophthalmology, Ehime University, Graduate School of Medicine, Ehime, Japan.
Hiroshi EguchiDepartment of Ophthalmology, Institute of Health Biosciences, University of Tokushima Graduate School, Tokushima, Japan.
Saichi HoshiFujieda Municipal General Hospital, Shizuoka, Japan.
Yoshitsugu InoueDivision of Ophthalmology and Visual Science, Faculty of Medicine, Tottori University, Tottori, Japan.
Hideki AizawaFurukawa Electric Co., Ltd., Tokyo, Japan.
Kazutomi MiyoshiFurukawa Electric Co., Ltd., Tokyo, Japan.
Michio OhkuboFurukawa Electric Co., Ltd., Tokyo, Japan.
Eiji HiwatashiDepartment of Ophthalmology, Ofuna Chuo Hospital, Kanagawa, Japan.
Hiroshi TachibanaDepartment of Infectious Diseases, Tokai University School of Medicine, Kanagawa, Japan.
Yuichi OhashiDepartment of Ophthalmology, Ehime University, Graduate School of Medicine, Ehime, Japan.
Ehime University · JPFurukawa Electric (Japan) · JPFujieda Municipal General Hospital · JPGunma Chuo Hospital · JPTokai University · JPTokushima University · JPTottori University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We developed an immunochromatographic assay kit that uses fluorescent silica nanoparticles bound to anti-Acanthamoeba antibodies (fluorescent immunochromatographic assay [FICGA]) and evaluated its efficacy for the detection of Acanthamoeba and diagnosis of Acanthamoeba keratitis (AK). The sensitivity of the FICGA kit was evaluated using samples of Acanthamoeba trophozoites and cysts diluted to various concentrations. A conventional immunochromatographic assay kit with latex labels (LICGA) was also evaluated to determine its sensitivity in detecting Acanthamoeba trophozoites. To check for cross-reactivity, the FICGA was performed by using samples of other common causative pathogens of infectious keratitis, such as Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, and Candida albicans. Corneal scrapings from patients with suspected AK were tested with the FICGA kit to detect the presence of Acanthamoeba, and the results were compared with those of real-time PCR. The FICGA kit detected organisms at concentrations as low as 5 trophozoites or 40 cysts per sample. There were no cross-reactivities with other pathogens. The FICGA was approximately 20 times more sensitive than the LICGA for the detection of Acanthamoeba trophozoites. The FICGA kit yielded positive results for all 10 patients, which corresponded well with the real-time PCR results. The FICGA kit demonstrated high sensitivity for the detection of Acanthamoeba and may be useful for the diagnosis of AK.

Indexed as

Fluorescent Antibody TechniqueNanoparticlesReagent Kits, DiagnosticSilicon DioxideAcanthamoebaAcanthamoeba KeratitisAdolescentAdultAntibodies, ProtozoanChromatography, AffinityFemaleHumansMaleMiddle AgedReproducibility of ResultsSensitivity and SpecificityAntibodies, ProtozoanReagent Kits, DiagnosticSilicon Dioxide

Identifiers

PMID25392356
PMCPMC4290933
OpenAlexW2021947806

What OpenQuestion holds

Textmetadata
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.