Evidence map›Paper›PMID 42515595›Full record

ArticleViruses2026

Detectability of Pathogenic RNA Virus Families in Different Body Sites: A Scoping Review.

Christian Schaadt Ilsby, Thomas Leineweber Kristensen, Kristian Bagge, Jens Bukh, Jan Gorm Lisby, Uffe Vest Schneider

Abstract readScoping Review
In one paragraph

Article in Viruses, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Christian Schaadt IlsbyDepartment of Virology and Microbiological Preparedness, Statens Serum Institut, 2300 Copenhagen, Denmark.ORCID 0000-0002-9029-203X
Thomas Leineweber KristensenDepartment of Virology and Microbiological Preparedness, Statens Serum Institut, 2300 Copenhagen, Denmark.ORCID 0000-0001-9377-0781
Kristian BaggeCopenhagen Hepatitis C Program (CO-HEP), Department of Immunology and Microbiology, University of Copenhagen, 2200 Copenhagen, Denmark.ORCID 0000-0002-7078-4002
Jens BukhCopenhagen Hepatitis C Program (CO-HEP), Department of Immunology and Microbiology, University of Copenhagen, 2200 Copenhagen, Denmark.ORCID 0000-0002-7815-4806
Jan Gorm LisbyDepartment of Clinical Microbiology, Copenhagen University Hospital-Hvidovre, 2650 Hvidovre, Denmark.ORCID 0000-0002-6416-7550
Uffe Vest SchneiderDepartment of Virology and Microbiological Preparedness, Statens Serum Institut, 2300 Copenhagen, Denmark.ORCID 0000-0003-1372-7885

Funding

The DURABLE project Project number: 101102733
6 · The paper itself

Abstract

Nucleic acid amplification tests (NAATs) are central to modern virology diagnostics. However, evidence supporting alternative specimen types remains uneven across viral families, especially for emerging viruses. This limits diagnostic flexibility in outbreak and clinically complex settings. We conducted a scoping review of NAAT detectability across key body sites for human RNA viruses. PubMed and Embase were systematically searched for studies reporting NAAT results from urine, blood, fecal, cerebrospinal fluid, or respiratory specimens. Data were independently screened and synthesized to summarize specimen-specific detectability for each virus. From 8676 screened records, 321 studies were included, covering 39 viruses across 25 RNA virus families. Detectability across specimen types varied substantially between viruses. Consistent detection across multiple specimens was observed for few viruses, including SARS-CoV-2, Zika virus, and HIV, whereas many emerging viruses were evaluated in a single body compartment with limited comparative data. NAAT performance across specimen types is highly virus-specific and unevenly studied, with reliance on blood or respiratory specimens, potentially overlooking viable, less invasive alternatives. Evidence gaps are particularly pronounced for urine and cerebrospinal fluid, and heterogeneous reporting limits cross-study comparability. Standardized, cross-specimen and longitudinal studies are needed to improve diagnostic strategies, outbreak preparedness, and future assay development.

Indexed as

Nucleic Acid Amplification TechniquesRNA VirusesRNA Virus InfectionsBody FluidsFecesHumansRNA, ViralUrineRNA, Viralbody sitesdiagnostic samplingRNA virusesscoping reviewviral detectionviral tropism

Identifiers

PMID42515595
PMCPMC13431510

What OpenQuestion holds

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Registered trials

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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.