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CADEM: Species-level detection of mycobacterial cfDNA via CRISPR for pulmonary disease diagnosis

Authors
 Park, Seungil  ;  Koo, Bonhan  ;  Kim, Myoung Gyu  ;  Lee, Eun Yeong  ;  Lee, Hyo Joo  ;  Roh, Yeonjeong  ;  Lee, Minju  ;  Bae, Chae Eun  ;  Lee, Sei Won  ;  Kang, Young Ae  ;  Shin, Yong 
Citation
 ANALYTICA CHIMICA ACTA, Vol.1388, 2026-02 
Article Number
 345085 
Journal Title
ANALYTICA CHIMICA ACTA
ISSN
 0003-2670 
Issue Date
2026-02
MeSH
CRISPR-Cas Systems* ; Cell-Free Nucleic Acids* / analysis ; Cell-Free Nucleic Acids* / blood ; Cell-Free Nucleic Acids* / genetics ; DNA, Bacterial* / blood ; DNA, Bacterial* / genetics ; Humans ; Lab-On-A-Chip Devices ; Lung Diseases* / diagnosis ; Lung Diseases* / microbiology ; Microfluidic Analytical Techniques ; Mycobacterium avium Complex / genetics ; Mycobacterium avium Complex / isolation & purification
Keywords
Mycobacterial pulmonary diseases ; CADEM assay ; cfDNA enrichment ; CRISPR-based detection ; Clinical applications
Abstract
Background: Pulmonary infections caused by Mycobacterium tuberculosis (MTB) and nontuberculous mycobacteria (NTM) present significant clinical challenges due to overlapping symptoms and different treatments. In particular, accurate identification of NTM species such as Mycobacterium avium complex (MAC) and Mycobacterium abscessus complex (MABC) is essential, as these species show drug susceptibility profiles that differ markedly from MTB. However, conventional culture-based diagnostics are time-consuming, and current molecular assays often lack resolution and rely heavily on sputum specimens. To address these limitations, liquid biopsy using bacterial-derived circulating cell-free DNA (cfDNA) offers a minimally invasive alternative, and CRISPR/Cas12a technology provides the sensitivity required to detect its low levels. Results: We developed CADEM (CRISPR-Assisted Detection via Enrichment of Mycobacterium-derived cfDNA using Microfluidic technology), a streamlined diagnostic system that integrates microfluidic cfDNA enrichment, targeted amplification, and CRISPR/Cas12a-based detection. The microfluidic platform enables high-yield recovery of cfDNA from large-volume clinical samples without the need for cell lysis. Optimized Cas12a-crRNA complexes enable highly sensitive and specific detection of MAC-, MABC-, and MTB-specific amplicons, achieving 10-to 100-fold greater sensitivity than end-point PCR and probe-based real-time PCR. In a validation set of 20 clinical specimens (7 positives and 13 healthy controls), CADEM identified all MAC, MABC, and MTB cases with full accuracy and no false positives. The CRISPR detection step produced a clear fluorescence readout within 20 min and, together with enrichment and amplification, delivered species-level results within a 2-h workflow. Significance: CADEM offers an accurate and streamlined molecular approach for distinguishing MAC, MABC, and MTB at the species-level to support appropriate diagnosis and treatment. By combining microfluidic cfDNA enrichment with CRISPR-based detection, CADEM enables efficient analysis from liquid biopsy samples for pulmonary disease diagnosis. The system is also compatible with isothermal amplification, supporting future adaptation for point-of-care testing in resource-limited settings.
Full Text
https://www.sciencedirect.com/science/article/pii/S0003267026000358
DOI
10.1016/j.aca.2026.345085
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kang, Young Ae(강영애) ORCID logo https://orcid.org/0000-0002-7783-5271
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/211044
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