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An automated and portable platform for rapid cell-free DNA isolation and its application in microbial DNA metagenomic sequencing from human blood samples

  • Linda Marriott
  • , Ana Martinez-Lopez
  • , Antonio Liga
  • , Kazuhiro Horiba
  • , Amanda Warr
  • , Jacob N. Phulusa
  • , Radhe Shantha Kumar
  • , Laura Carey
  • , Yoshinori Ito
  • , Benjamin J. Parcell
  • , Nicholas R. Leslie
  • , Nicholas A. Feasey
  • , Shevin T. Jacob
  • , Jamie Rylance
  • , Maïwenn Kersaudy-Kerhoas
  • Heriot-Watt University
  • University of Edinburgh
  • National Institute of Infectious Diseases
  • Kamuzu University of Health Sciences
  • University of Cambridge
  • Aichi Medical University
  • University of Dundee
  • University of St Andrews

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

The prompt identification of pathogens in human circulation in a clinically deployable format remains an unmet clinical need. The established test for infection diagnostics remains blood culture, which typically takes 2–4 days and is positive in less than 15% of cases, with many prevalent pathogens difficult or impossible to culture. While microbial cfDNA in blood could facilitate the diagnosis of sepsis, febrile and infectious conditions, sample preparation for cell-free DNA (cfDNA) analysis in decentralised settings presents challenges due to its complexity and the low concentration and fragmented nature of cfDNA in blood plasma. We developed a portable and automated platform and a consumable (CNASafe) for cfDNA isolation from human plasma samples. The platform-device performance was evaluated by comparing relative cfDNA yield against a reference (QIAGEN QIAamp Circulating Nucleic Acid Kit). cfDNA eluates from ten non-cultured blood samples from hospital patients were sequenced on a nanopore sequencer, and results compared to blood cultures. Extraction of cfDNA using the CNASafe device was completed in 40 minutes, compared to the 1 hour 15 min reference protocol. The device achieved an average relative cfDNA recovery of 100.5% over 333 unique extractions encompassing all parameter variations, demonstrating a performance equivalent to the reference kit. From the patient samples, a sufficient quantity of microbial cfDNA was extracted to either identify pathogens missed by blood cultures or confirm negative cultures. The CNASafe platform and real-time nanopore sequencing offer a promising solution for the rapid deployment of metagenomic diagnostics, enabling pathogen identification within a few hours in decentralised clinical environments.

Original languageEnglish
Pages (from-to)2849-2860
Number of pages12
JournalLab on a Chip
Volume26
Issue number9
DOIs
Publication statusAccepted/In press - 6 Feb 2026

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