Evidence map›Paper›PMID 42396090›Full record

ArticleACS omega2026

CRISPR/Cas12a2-Mediated Ultrasensitive Assay for Rapid Detection of H1N1 Influenza Virus RNA.

Chunlin Wen, Xiangyang Min, Helin Yu, Kai Jin, Wenwen Jing, Feifei Wang, Xunjia Cheng, Liulin Luo, Meng Feng

Abstract read
In one paragraph

Article in ACS omega, 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

9 authors.

Chunlin WenShanghai Institute of Infectious Disease and Biosecurity, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
Xiangyang MinDepartment of Clinical Laboratory, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China.
Helin YuShanghai Institute of Infectious Disease and Biosecurity, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
Kai JinDepartment of Surgical Intensive Care Unit, HuaDong Hospital Affiliated to Fudan University, Shanghai 200040, China.
Wenwen JingShanghai Institute of Infectious Disease and Biosecurity, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.ORCID https://orcid.org/0000-0003-1038-5509
Feifei WangShanghai Institute of Infectious Disease and Biosecurity, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
Xunjia ChengShanghai Institute of Infectious Disease and Biosecurity, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.ORCID https://orcid.org/0000-0002-8851-6903
Liulin LuoDepartment of Clinical Laboratory, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China.
Meng FengShanghai Institute of Infectious Disease and Biosecurity, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The H1N1 influenza virus poses a major global public health challenge, highlighting an urgent demand for advanced diagnostic technologies that enable rapid and accurate detection. This study established a novel CRISPR-Cas12a2-based diagnostic platform for highly sensitive and rapid detection of influenza A H1N1 virus. Targeting the conserved M gene, the assay combined optimized crRNA design with the unique dual RNA cleavage and collateral ssDNA degradation activities of SuCas12a2, enabling fluorescence-based detection with a sensitivity of 5 copies/μL. Clinical validation of 205 nasopharyngeal swabs demonstrated 91.22% concordance with real-time qPCR (κ = 0.65) and identified 18 additional positive cases, indicating superior sensitivity. The assay achieved a detection limit of 5 RNA copies/μL within 90 min by combining through a reverse transcription PCR with CRISPR detection. Rigorous specificity testing confirmed 100% discrimination against other respiratory pathogens. These results positioned CRISPR-Cas12a2 as a robust diagnostic alternative, offering advantages in speed and sensitivity. This technology represents a significant advancement in molecular diagnostics, meeting the critical needs for rapid and accurate pathogen detection during outbreaks.

Identifiers

PMID42396090
PMCPMC13325098

What OpenQuestion holds

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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.