Evidence map›Paper›PMID 41428300›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2026

Establishment and application of multiple cross displacement amplification coupled with lateral flow biosensor (MCDA-LFB) for visual and rapid detection of Candida glabrata.

Yan Yuan, Yuhong Zhou, Yanfeng Zhou, Rui Ye, Jingrun Lu, Yizhe Wang, Fang Wei, Fukuan He, Honglan Yu, Yu Wang

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Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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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

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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. Rapid and ultrasensitive detection ofFrontiers in cellular and infection microbiology · 2026
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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Yan YuanDepartment of Clinical Laboratory, The First People's Hospital of Guiyang, Guiyang, China.
Yuhong ZhouDepartment of Clinical Laboratory, The First People's Hospital of Guiyang, Guiyang, China.
Yanfeng ZhouDepartment of Basic Clinical Laboratory Medicine, School of Clinical Laboratory Science, Guizhou Medical University, Guiyang, Guizhou Province, China.
Rui YeDepartment of Clinical Laboratory, The First People's Hospital of Guiyang, Guiyang, China.
Jingrun LuDepartment of Clinical Laboratory, The First People's Hospital of Guiyang, Guiyang, China.
Yizhe WangDepartment of Clinical Laboratory, The First People's Hospital of Guiyang, Guiyang, China.
Fang WeiDepartment of Clinical Laboratory, The First People's Hospital of Guiyang, Guiyang, China.
Fukuan HeDepartment of Clinical Laboratory, The First People's Hospital of Guiyang, Guiyang, China.
Honglan YuDepartment of Clinical Laboratory, The First People's Hospital of Guiyang, Guiyang, China. 1049251463@qq.com.
Yu WangDepartment of Clinical Laboratory, The First People's Hospital of Guiyang, Guiyang, China. wangzhongyuwy@163.com.

Funding

Science and Technology Department of Guiyang city of Guizhou Province. Zhu Ke He Tong (2020)-10-6, Zhu ke he tong [2021]-43-25 and GCC [2023]030Science and Technology Department of Guizhou Province Qian Ke He Zhi Cheng [2021] yi ban 440the Guiyang High-level Innovative Youth Health Talent Training Program Zhu Wei Jian Ke Ji He Tong [2023]-011
6 · The paper itself

Abstract

background(Candida glabrata C. glabrata) is classified as a high-priority pathogen by the World Health Organization (WHO). It causes mucosal and deep infections in immunocompromised individuals, yet its diagnosis currently relies on slow culture processes. This highlights the urgent need for rapid and accurate detection methods.

methodsTen primers targeting different regions of the C. glabrata ITS2 gene were designed to create a multiple cross displacement amplification (MCDA) assay coupled with a nanoparticle lateral flow biosensor (LFB). Following optimisation of temperature and time, the multiple cross displacement amplification coupled with lateral flow biosensor (MCDA-LFB) system was employed to detect C. glabrata DNA in clinical specimens.

resultsUnder optimal conditions (63 °C, 40 min), the C. glabrata-MCDA-LFB assay achieved a limit of detection (LoD) of 10 fg/µL.The assay successfully detected all C. glabrata strains tested and demonstrated no cross-reactivity with non-C. glabrata isolates. Findings showed that the C. glabrata-MCDA-LFB assay promptly and successfully detected all 57 C. glabrata-positive samples among 240 clinical specimens identified by traditional culture methods. The entire process, including sample processing (20 min), the MCDA reaction (40 min) and result documentation (2 min), was completed within 62 min.

conclusionThe C. glabrata-MCDA-LFB assay developed in this study is a rapid, simplified, sensitive and specific technique that is straightforward to use. It can be used to screen for or diagnose C. glabrata infections in clinical settings, particularly in regions with limited resources.

Indexed as

Biosensing TechniquesCandida glabrataCandidiasisMolecular Diagnostic TechniquesNucleic Acid Amplification TechniquesDNA, FungalDNA PrimersHumansLimit of DetectionSensitivity and SpecificityDNA, FungalDNA PrimersCandida glabrataC. glabrata-MCDA-LFBLateral flow biosensorMultiple cross displacement amplification

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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.