Evidence map›Paper›PMID 41310300›Full record

ArticleWorld journal of microbiology & biotechnology2025

Development and application of a rapid dual RPA-LFS assay for simultaneous detection of Enterococcus faecalis and Enterococcus faecium.

Yang Wang, Zhongfang Dai, Wenjun Zhu, Lei Wang, Hongchun Li

Abstract read
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In one paragraph

Article in World journal of microbiology & 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. Simultaneous point-of-care detection and virulence typing of Helicobacter pylori using multiplex recombinase polymerase amplification combined with lateral flow strip.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
  2. Establishment and clinical application of a rapid RPA-LFS assay for detectingFrontiers in cellular and infection microbiology · 2026
    Article
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

5 authors.

Yang Wang *Department of Oncology, The Affiliated Lianyungang Hospital of Xuzhou Medical University, (The First People's Hospital of Lianyungang), Lianyungang, Jiangsu, China.
Zhongfang Dai *Department of Laboratory Medicine, The Affiliated Lianyungang Hospital of Xuzhou Medical University, (The First People's Hospital of Lianyungang), Lianyungang, Jiangsu, China.
Wenjun ZhuDepartment of Laboratory Medicine, The Second People's Hospital of Lianyungang, Lianyungang, Jiangsu, China.
Lei WangDepartment of Laboratory Medicine, The Affiliated Lianyungang Hospital of Xuzhou Medical University, (The First People's Hospital of Lianyungang), Lianyungang, Jiangsu, China. wangleiwendy@126.com.
Hongchun LiMedical Technology College, Xuzhou Medical University, Xuzhou, Jiangsu, China. lihongchun@xzhmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enterococcus faecium and Enterococcus faecalis, ranked among the top three global nosocomial pathogens (WHO data), pose escalating threats due to multidrug resistance (particularly vancomycin-resistant strains, VRE) and foodborne transmission. Conventional detection relies on time-consuming culture-based typing (ISO 7899-2; 48-72 h) with > 12% false-negative rates, while molecular methods like qPCR require sophisticated instrumentation, limiting field deployment. This study developed a rapid dual recombinase polymerase amplification-lateral flow strip (RPA-LFS) assay for simultaneous detection of E. faecium and E. faecalis, addressing critical bottlenecks of prolonged turnaround time, species differentiation challenges, and equipment dependency. Species-specific primers and probes were designed targeting conserved genomic regions. Probes featured 5'-FITC/DIG reporter groups and amplification products incorporated 3'-biotin modifications, enabling THF cleavage-mediated signal release. Following optimization (37 °C, 20 min), results were visually interpreted via LFS within 10 min. Key findings include: Sensitivity: 10 CFU/mL (E. faecalis) and 10

Indexed as

Enterococcus faecalisEnterococcus faeciumGram-Positive Bacterial InfectionsNucleic Acid Amplification TechniquesDNA, BacterialHumansRecombinasesSensitivity and SpecificityDNA, BacterialRecombinasesEnterococcus faecalisEnterococcus faeciumLFSRPA

Identifiers

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.