Evidence map›Paper›PMID 41316351›Full record

ArticleParasites & vectors2025

Development of a field-deployable RPA-CRISPR/Cas12a assay for the detection of Cyclospora cayetanensis in human feces.

Ziyang Qin, Yilin Wang, Mengqing Sun, Qinglin Wang, Junxia Duan, Chunhao Gu, Xinfu Zhang, Fuchang Yu, Yayun Wu, Huiyan Xu and 2 more

Abstract read
In one paragraph

Article in Parasites & vectors, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

12 authors.

Ziyang QinCollege of Veterinary Medicine, Henan Agricultural University, No. 218 of Ping An Avenue, Zhengdong Newly-Developed Area, Zhengzhou, 450046, People's Republic of China.
Yilin WangCollege of Veterinary Medicine, Henan Agricultural University, No. 218 of Ping An Avenue, Zhengdong Newly-Developed Area, Zhengzhou, 450046, People's Republic of China.
Mengqing SunCollege of Veterinary Medicine, Henan Agricultural University, No. 218 of Ping An Avenue, Zhengdong Newly-Developed Area, Zhengzhou, 450046, People's Republic of China.
Qinglin WangCollege of Veterinary Medicine, Henan Agricultural University, No. 218 of Ping An Avenue, Zhengdong Newly-Developed Area, Zhengzhou, 450046, People's Republic of China.
Junxia DuanCollege of Veterinary Medicine, Henan Agricultural University, No. 218 of Ping An Avenue, Zhengdong Newly-Developed Area, Zhengzhou, 450046, People's Republic of China.
Chunhao GuCollege of Veterinary Medicine, Henan Agricultural University, No. 218 of Ping An Avenue, Zhengdong Newly-Developed Area, Zhengzhou, 450046, People's Republic of China.
Xinfu ZhangCollege of Veterinary Medicine, Henan Agricultural University, No. 218 of Ping An Avenue, Zhengdong Newly-Developed Area, Zhengzhou, 450046, People's Republic of China.
Fuchang YuCollege of Animal Science and Technology, Tarim University, Alar, Xinjiang, 843300, People's Republic of China.
Yayun WuCollege of Veterinary Medicine, Henan Agricultural University, No. 218 of Ping An Avenue, Zhengdong Newly-Developed Area, Zhengzhou, 450046, People's Republic of China.
Huiyan XuCollege of Veterinary Medicine, Henan Agricultural University, No. 218 of Ping An Avenue, Zhengdong Newly-Developed Area, Zhengzhou, 450046, People's Republic of China.
Junqiang LiCollege of Veterinary Medicine, Henan Agricultural University, No. 218 of Ping An Avenue, Zhengdong Newly-Developed Area, Zhengzhou, 450046, People's Republic of China. lijunqiangcool@126.com.
Longxian ZhangCollege of Veterinary Medicine, Henan Agricultural University, No. 218 of Ping An Avenue, Zhengdong Newly-Developed Area, Zhengzhou, 450046, People's Republic of China. zhanglx8999@henau.edu.cn.

Funding

Henan Province Scientific and Technological Project 232102110088Key Research and Development Project of Henan Province 231111111500National Key Research and Development Program of China 2023YFD1801200
6 · The paper itself

Abstract

backgroundCyclospora is an emerging intestinal pathogenic protozoan transmitted through foodborne and waterborne routes. At least 19 countries in the world have recorded outbreaks of cyclosporiasis, mainly associated with the consumption of contaminated fresh agricultural products. The lack of a sensitive immediate test is one of the major obstacles to the rapid diagnosis of cyclosporiasis. The target interference mechanisms of clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) protein systems have been adapted into versatile and efficient genome manipulation and disease-curing technologies, while also being promising for point-of-care testing (POCT) applications. It can serve as an excellent rapid and specific detection tool.

methodsThe recombinase polymerase amplification (RPA) and the CRISPR/Cas12a system were combined to develop a detection method for C. cayetanensis (termed RECCT-Cay) via visual observation of fluorescent readings under blue light and field diagnosis using lateral flow strip (LFS) biosensors.

resultsThe detection limit of the established RECCT-Cay was 7 copies/μL. Under simulated clinical conditions, the detection limit was 30 oocysts per gram of stool. At the same time, the established detection platform can distinguish C. cayetanensis from the closely related Eimeria spp. The results of our constructed assay were compared with nested PCR, and the detection results of 30 clinical stool samples were consistent, with three samples positive for C. cayetanensis. Based on the RECCT-Cay detection principle, a portable suitcase-sized device has been designed, which can conduct rapid on-site detection of clinical samples.

conclusionsThe RECCT-Cay platform features rapid speed, high sensitivity, and the capability for field detection, making it a promising tool for use in remote areas.

Indexed as

CRISPR-Cas SystemsCyclosporaCyclosporiasisFecesMolecular Diagnostic TechniquesNucleic Acid Amplification TechniquesBiosensing TechniquesHumansRecombinasesSensitivity and SpecificityRecombinasesCRISPR/Cas12aCyclospora cayetanensisOn-site detectionRecombinase polymerase amplificationVisualized detection

Identifiers

PMID41316351
PMCPMC12763960

What Socratic holds

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LicenceCC BY
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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 Socratic graph.