Evidence map›Paper›PMID 40895317›Full record

ArticlePhenomics (Cham, Switzerland)2025

MVPCR: Multiplex Visual Detection Strategy Based on Ultrafast PCR for Point-of-Care Pathogens Detection Within 10 Min.

Ziqin Zhang, Cui Wu, Linlin Bai, Kaiming Guo, Ting Wang, Dianwei Liu, Mingrui Zhu, Feng Qian, Fang Zhang, Rui Wang

Abstract read
In one paragraph

Article in Phenomics (Cham, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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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

10 authors.

Ziqin Zhang *College of Biological Science and Engineering, Fuzhou University, Fuzhou, 350108 China.ORCID 0009-0008-4754-719X
Cui Wu *School of Biosystems Engineering and Food Science, ZJU-Hangzhou Global Scientific and Technological Innovation Center, Zhejiang University, Hangzhou, 310058 China.ORCID 0000-0002-8946-9918
Linlin BaiHuman Phenome Institute, State Key Laboratory of Genetic Engineering, School of Life Science, Fudan University, Shanghai, 200438 China.
Kaiming GuoHuman Phenome Institute, State Key Laboratory of Genetic Engineering, School of Life Science, Fudan University, Shanghai, 200438 China.
Ting WangDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen Peking University-The Hong Kong University of Science and Technology Medical Center, Shenzhen, 518036 China.
Dianwei LiuHuman Phenome Institute, State Key Laboratory of Genetic Engineering, School of Life Science, Fudan University, Shanghai, 200438 China.
Mingrui ZhuHuman Phenome Institute, State Key Laboratory of Genetic Engineering, School of Life Science, Fudan University, Shanghai, 200438 China.
Feng QianHuman Phenome Institute, State Key Laboratory of Genetic Engineering, School of Life Science, Fudan University, Shanghai, 200438 China.
Fang ZhangCollege of Biological Science and Engineering, Fuzhou University, Fuzhou, 350108 China.ORCID 0000-0001-5323-6728
Rui WangHuman Phenome Institute, State Key Laboratory of Genetic Engineering, School of Life Science, Fudan University, Shanghai, 200438 China.ORCID 0000-0003-2945-2046

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogens pose significant threats to biosecurity and environmental health due to their potential for widespread outbreaks. Effective pathogen detection requires methods that are rapid, sensitive, specific, and informative. Here, we proposed a multiplex visual detection system that integrated ultrafast polymerase chain reaction (PCR) and molecular beacons, allowing the simultaneous detection of three pathogens in a one-pot reaction. The ultrafast PCR protocol employed cycles of just 7 s each, allowing the entire process-from sampling to result-to be completed within only 10 min. Molecular beacons hybridized with target sequences during ultrafast PCR, generating fluorescence signals that are visually detectable without specialized equipment. Additionally, we developed a compact, portable cartridge integrated with online software for fluorescence visualization and direct result output, eliminating the need for bulky instruments and specialized personnel, thereby facilitating point-of-care testing (POCT). The method demonstrated high specificity and sensitivity, with a limit of detection (LOD) as low as 23 copies per reaction. It achieved a 100% positive detection rate in practical applications, performing comparably to standard PCR. Furthermore, the method effectively identified low concentrations of pathogens in animal infection samples. This ultrafast, highly sensitive, specific, and informative method shows significant potential for POCT applications, including food safety monitoring and clinical diagnostics. Supplementary Information: The online version contains supplementary material available at 10.1007/s43657-024-00216-3.

Indexed as

Molecular beaconMultiple pathogens detectionPoint-of-care testingUltrafast polymerase chain reactionVisual strategy

Identifiers

PMID40895317
PMCPMC12390895

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.