Evidence map›Paper›PMID 41599009›Full record

ArticlePathogens (Basel, Switzerland)2025

Rapid and Simple Detection of

Yue-Rong Lv, Yi-Yang Liu, Rong Zhang, Bo Yang, Shi-Yuan Xue, Yu-Lin Ding, Jun-Tao Jia, Hasi Bayaer, Alateng Bagen, Rui-Bin Chen and 3 more

Abstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Yue-Rong LvCollege of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China.ORCID 0009-0001-1337-3901
Yi-Yang LiuCollege of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China.
Rong ZhangOtok Banner Animal Disease Prevention and Control Center, Ordos 016100, China.
Bo YangAnimal Disease Control Center of Ordos, Ordos 016100, China.
Shi-Yuan XueCollege of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China.ORCID 0009-0000-1640-7890
Yu-Lin DingCollege of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China.
Jun-Tao JiaCollege of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China.
Hasi BayaerOtok Banner Animal Disease Prevention and Control Center, Ordos 016100, China.
Alateng BagenOtok Banner Animal Disease Prevention and Control Center, Ordos 016100, China.
Rui-Bin ChenOtok Banner Animal Disease Prevention and Control Center, Ordos 016100, China.
Siqin TunalaOtok Banner Animal Disease Prevention and Control Center, Ordos 016100, China.
Li ZhaoCollege of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China.ORCID 0000-0001-8538-5605
Yong-Hong LiuCollege of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China.ORCID 0000-0003-4432-9433

Funding

1.Ordos Science & Technology Plan 2.Special Project for the Construction of Scientific Research and Innovation Teams, Class B Team 3.Inner Mongolia Autonomous Region First Class Discipline Research Special Project 1.(YF20240007) 2.(BR251303) 3.(YLXKZX-NND-012)
6 · The paper itself

Abstract

Paratuberculosis (PTB), caused by Mycobacterium avium subsp. paratuberculosis (MAP), is a chronic intestinal disease in ruminants. PTB is difficult to diagnose, control, and eradicate, leading to substantial economic losses. Thus, sensitive and specific detection methods are urgently required. crRNA and primers targeting the MAP ATPase FtsK gene were designed for recombinase polymerase amplification (RPA) and nested PCR. Fecal DNA was amplified using RPA or nested PCR, purified with Tris-saturated phenol-chloroform-isoamyl alcohol, and detected via CRISPR-Cas12a. Moreover, signals were read using a qPCR instrument, fluorescence reader, or lateral flow strips. RPA-CRISPR-Cas12a and nested PCR-CRISPR-Cas12a assays were optimized and validated on 50 clinical samples and 7 MAP cultures. The limits of detection were 1 × 10

Indexed as

CRISPR-Cas SystemsMycobacterium avium subsp. paratuberculosisParatuberculosisPolymerase Chain ReactionAnimalsCattleDNA, BacterialFecesRapid Diagnostic TestsRecombinasesSensitivity and SpecificityDNA, BacterialRecombinasesCRISPR-Cas12aMycobacterium avium subsp. paratuberculosisnested PCRRPA

Identifiers

PMID41599009
PMCPMC12845311

What OpenQuestion holds

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LicenceCC BY
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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.