4.5 Article

Simultaneous detection of multiple bacterial and viral aquatic pathogens using a fluorogenic loop-mediated isothermal amplification-based dual-sample microfluidic chip

Journal

JOURNAL OF FISH DISEASES
Volume 44, Issue 4, Pages 401-413

Publisher

WILEY
DOI: 10.1111/jfd.13325

Keywords

aquatic pathogen; dual‐ sample microfluidic chip; loop‐ mediated isothermal amplification; multiplex detection; real‐ time detection

Funding

  1. Program of Science and Technology Department of Zhejiang Province [LGN18C180002]
  2. State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products [KF20200105, 2010DS700124ZZ2008]
  3. Scientific Innovation Team Project of Ningbo [2015C110018]
  4. Natural Science Foundation of Ningbo [2018A610342]
  5. Zhejiang Key Laboratory of Exploitation and Preservation of Coastal Bio-resource [J2018004]
  6. Jiangbei Agricultural and Social Development Science and Technology Project [2017B02]

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A dual-sample microfluidic chip integrated with real-time fluorogenic loop-mediated isothermal amplification assay was developed for simultaneous detection of 10 pathogenic microorganisms in aquaculture, achieving high clinical sensitivity and specificity.
Rapid and user-friendly diagnostic tests are necessary for early diagnosis and immediate detection of diseases, particularly for on-site screening of pathogenic microorganisms in aquaculture. In this study, we developed a dual-sample microfluidic chip integrated with a real-time fluorogenic loop-mediated isothermal amplification assay (dual-sample on-chip LAMP) to simultaneously detect 10 pathogenic microorganisms, that is Aeromonas hydrophila, Edwardsiella tarda, Vibrio harveyi, V. alginolyticus, V. anguillarum, V. parahaemolyticus, V. vulnificus, infectious hypodermal and haematopoietic necrosis virus, infectious spleen and kidney necrosis virus, and white spot syndrome virus. This on-chip LAMP provided a nearly automated protocol that can analyse two samples simultaneously, and the tests achieved limits of detection (LOD) ranging from 10(0) to 10(-1) pg/mu l for genomic DNA of tested bacteria and 10(-4) to 10(-5) pg/mu l for recombinant plasmid DNA of tested viruses, with run times averaging less than 30 min. The coefficient of variation for the time-to-positive value was less than 10%, reflecting a robust reproducibility. The clinical sensitivity and specificity were 93.52% and 85.53%, respectively, compared to conventional microbiological or clinical methods. The on-chip LAMP assay provides an effective dual-sample and multiple pathogen analysis, and thus would be applicable to on-site detection and routine monitoring of multiple pathogens in aquaculture.

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