Evidence map›Paper›PMID 36653150›Full record

ArticleThe Journal of veterinary medical science2023

Simple and rapid detection of severe fever with thrombocytopenia syndrome virus in cats by reverse transcription-loop-mediated isothermal amplification (RT-LAMP) assay using a dried reagent.

Keita Ishijima, Kota Yokono, Eunsil Park, Masakatsu Taira, Kango Tatemoto, Yudai Kuroda, Milagros Virhuez Mendoza, Yusuke Inoue, Michiko Harada, Aya Matsuu and 3 more

Open access · diamondAbstract read
In one paragraph

Article in The Journal of veterinary medical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. 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

13 authors at 3 institutions in 1 country.

Keita IshijimaDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo, Japan.
Kota YokonoEiken Chemical Co., Ltd., Tokyo, Japan.
Eunsil ParkDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo, Japan.
Masakatsu TairaDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo, Japan.
Kango TatemotoDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo, Japan.
Yudai KurodaDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo, Japan.
Milagros Virhuez MendozaDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo, Japan.
Yusuke InoueDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo, Japan.
Michiko HaradaDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo, Japan.
Aya MatsuuDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo, Japan.
Shigeru MorikawaFaculty of Veterinary Medicine, Okayama University of Science, Ehime, Japan.
Shuetsu FukushiDepartment of Virology 1, National Institute of Infectious Diseases, Tokyo, Japan.
Ken MaedaDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo, Japan.
National Institute of Infectious Diseases · JPOkayama University of Science · JPYamaguchi University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe fever with thrombocytopenia syndrome virus (SFTSV) causes lethal hemorrhagic diseases in human, cats, and dogs. Several human cases involving direct transmission of SFTSV from diseased animals have been reported. Therefore, rapid diagnosis in veterinary clinics is important for preventing animal-to-human transmission. Previously, we developed a simplified reverse transcription-loop-mediated isothermal amplification (RT-LAMP) assay for human that does not require RNA extraction for detecting the SFTSV genome. In this study, we improved the simplified RT-LAMP assay for cats by introducing a dried reaction reagent and investigated the applicability of this method for diagnosing SFTS in cats. SFTSV RNA was detected in 11 of 12 cats naturally infected with SFTSV by RT-LAMP assay using both liquid and dried reagents. The RT-LAMP assay using liquid and dried reagents was also applicable to the detection of SFTSV genes 3-4 days after challenge in cats experimentally infected with SFTSV. The minimum copy number of SFTSV genes for 100% detection using the RT-LAMP assay with liquid and dried reagents was 4.3 × 10

Indexed as

Cat DiseasesDog DiseasesPhlebovirusSevere Fever with Thrombocytopenia SyndromeAnimalsCatsDogsHumansIndicators and ReagentsMolecular Diagnostic TechniquesNucleic Acid Amplification TechniquesRNA, ViralSensitivity and SpecificityIndicators and ReagentsRNA, Viralcatreverse transcription-loop-mediated isothermal amplificationreverse transcription-polymerase chain reactionsevere fever with thrombocytopenia syndrome viruszoonosis

Identifiers

PMID36653150
PMCPMC10076197
OpenAlexW4317037165

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.