Evidence map›Paper›PMID 36840574›Full record

ArticleJournal of clinical microbiology2023

Molecular Analysis of Rabies Virus Using RNA Extracted from Used Lateral Flow Devices.

Jaira D Mauhay, Nobuo Saito, Kazunori Kimitsuki, Milagros R Mananggit, Jeffrey L Cruz, Maria G Lagayan, Alyssa M Garcia, Patricia M Lacanilao, Kentaro Yamada, Mariko Saito-Obata and 4 more

Open access · hybridFull text read
In one paragraph

Article in Journal of clinical microbiology, 2023. 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
1.1field-weighted citation impact, top 24% 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, 8 citations in OpenAlex.

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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

14 authors at 5 institutions in 2 countries.

Jaira D MauhayDepartment of Microbiology, Faculty of Medicine, Oita University, Yufu, Oita, Japan.
Nobuo SaitoDepartment of Microbiology, Faculty of Medicine, Oita University, Yufu, Oita, Japan.ORCID 0000-0002-4396-5000
Kazunori KimitsukiDepartment of Microbiology, Faculty of Medicine, Oita University, Yufu, Oita, Japan.
Milagros R MananggitRegional Animal Disease Diagnostic Laboratory, Department of Agriculture Field Office III, San Fernando, Pampanga, Philippines.
Jeffrey L CruzDepartment of Agriculture, Bureau of Animal Industry, Quezon, National Capital Region, Philippines.
Maria G LagayanDepartment of Agriculture, Bureau of Animal Industry, Quezon, National Capital Region, Philippines.
Alyssa M GarciaDepartment of Microbiology, Faculty of Medicine, Oita University, Yufu, Oita, Japan.
Patricia M LacanilaoDepartment of Microbiology, Faculty of Medicine, Oita University, Yufu, Oita, Japan.
Kentaro YamadaLaboratory of Veterinary Public Health, Department of Veterinary Medical Science, Faculty of Agriculture, University of Miyazaki, Miyazaki, Miyazaki, Japan.
Mariko Saito-ObataTohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.
Daria L ManaloResearch Institute for Tropical Medicine, Muntinlupa, National Capital Region, Philippines.
Catalino S DemetriaResearch Institute for Tropical Medicine, Muntinlupa, National Capital Region, Philippines.
Beatriz P QuiambaoResearch Institute for Tropical Medicine, Muntinlupa, National Capital Region, Philippines.
Akira NishizonoDepartment of Microbiology, Faculty of Medicine, Oita University, Yufu, Oita, Japan.
Oita University · JPResearch Institute for Tropical Medicine · PHBureau of Plant Industry · PHTohoku University · JPUniversity of Miyazaki · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular analysis of rabies virus can provide accurate diagnosis and information on its genetic diversity. The transportation of rabies brain samples from remote areas to a central laboratory is challenging owing to biohazard risks and decomposability. We investigated the utility of used lateral flow devices (LFDs) for subsequent molecular analysis and assessed the necessary storage temperatures. Using RNA extracted from used LFD strips, we performed conventional reverse transcription-PCR (RT-PCR) using an LN34 primer set to amplify short fragments (165 bp) for rabies virus detection and the P1-304 primer set to amplify long fragments of the entire N gene amplicon (1,506 bp) for phylogenetic analysis. Among 71 used LFDs stored in a refrigerator and 64 used LFDs stored at room temperature, the LN34 assay showed high sensitivities (96.2% and 100%, respectively) for the diagnosis of rabies, regardless of the storage temperature. A significant reduction in the sensitivity of rabies diagnosis was observed when using the P1-304 primer set for used LFDs stored at room temperature compared to those stored at refrigeration temperature (20.9% versus 100%;

Indexed as

RabiesRabies virusHumansPhylogenyPolymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionRNA, ViralSensitivity and SpecificityRNA, Virallateral flow devicesmolecular methodsPhilippinesrabies

Identifiers

PMID36840574
PMCPMC10035306
OpenAlexW4321493435

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read47
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.