ArticleVirology journal2025
Establishment and comparison of RF-RAA and qPCR for rapid detection of Chinese soft-shelled turtle adenovirus (CSTAdV).
Article in Virology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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.
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.
Who cites it
2 citing papers in PubMed.
- Logistics-Mediated Artificial Sympatry and Its Implications for Molecular Detection ofInsects · 2026Article
- Development and evaluation of a recombinase-aided amplification-lateral flow dipstick assay for rapid and sensitive detection ofFrontiers in cellular and infection microbiology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
backgroundChinese soft-shelled turtle adenovirus (CSTAdV) is a new virus discovered recently that infects farmed Chinese soft-shelled turtle. In order to investigate its epizootiology and meet the requirements of timely prevention and control, it is imperative to establish an efficient diagnostic assay for CSTAdV.
resultsIn this study, on-site diagnostic real-time fluorescence Recombinase-aided amplification (RF-RAA) and real-time quantitative polymerase chain reaction (qPCR) detection methods were established based on the specific sequence of the viral DNA polymerase gene. The results showed that the sensitivity of the CSTAdV RF-RAA assay and qPCR assay was 1.0 × 10
conclusionsTherefore, the RF-RAA and qPCR assays provide two novel alternatives for simple, sensitive and specific identification of CSTAdV for pathogen screening in the field and quantitative analysis in the laboratory.
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Registered trials
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