Evidence map›Paper›PMID 40861863›Full record

ArticleFrontiers in bioengineering and biotechnology2025

A light-controlled one-tube detection platform combining CRISPR-Cas12a and RPA: an innovative approach for rapid diagnosis of

Zihan Zhou, Lele Pan, Shihua Luo, Jiangmei Ma, Baoyan Ren, Lina Liang, Xuebin Li, Guijiang Wei

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2025. 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
–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

2 citing papers in PubMed.

  1. Emerging point-of-care technologies for bacterial pathogen detection.Journal of Zhejiang University. Science. B · 2026
    Review
  2. Review
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

8 authors.

Zihan Zhou *Center for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Guangxi, Baise, China.
Lele PanCenter for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Guangxi, Baise, China.
Shihua LuoCenter for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Guangxi, Baise, China.
Jiangmei MaCenter for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Guangxi, Baise, China.
Baoyan RenYaneng BlOscience (Shenzhen) Corporation, Guangdong, Shenzhen, China.
Lina LiangCenter for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Guangxi, Baise, China.
Xuebin LiBaise Key Laboratory for Precise Genetic Testing of Long-dwelling Nationalities, Guangxi, Baise, China.
Guijiang WeiCenter for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Guangxi, Baise, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Methods: We have developed a one-tube detection method for UV light unlocking based on RPA-CRISPR/Cas12a technology. This method utilizes the photodegradable chemical group NPOM-dt to chemically modify the crRNA base, preventing it from complementary pairing with the base of the target molecule, thereby temporarily silencing the CRISPR system. After RPA preamplification, the caged modification group on the crRNA was removed with brief irradiation with ultraviolet light to restore the activity of the CRISPR/Cas12a. system. Results: Our results demonstrated that the detection system achieved a limit of detection as low as 10 copies/μL for target fragments, with no cross-reactivity observed with genomic DNA from six clinically common pathogenic bacteria, showcasing excellent sensitivity and specificity. Additionally, clinical validation was performed using 38 sputum samples. The system successfully identified A. baumannii in sputum specimens, with results consistent with those obtained via conventional PCR. Conclusion: We have successfully developed a light-controlled one-tube RPA-CRISPR/Cas12a detection system. It simplifies the operation and at the same time greatly reduces the risk of laboratory contamination caused by repeated tube opening, providing a new idea for the development of point-of-care testing (POCT).

Indexed as

Acinetobacter baumanniiCRISPR/Cas12aNPOM-dtone-tube detectionPOCT

Identifiers

PMID40861863
PMCPMC12375640

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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.