Borrelia-specific cell-free DNA in plasma from adults with Lyme neuroborreliosis: an explorative study

Current blood-based diagnostic modalities for LNB have significant limitations. Using Next Generation Sequencing, we investigated blood samples from patients with LNB and non-LNB controls for Borrelia burgdorferi-specific cfDNA (Bb-cfDNA). Blood-samples from 61 adults suspected for LNB were analysed with amplification-free Nanopore metagenomic sequencing and detected cfDNA was cross-referenced with human and Bb-genome databases to identify Bb-specific-cfDNA. Bb-cfDNA was detected in 3 of 45 patients with LNB (6.7%) and in none of the 16 controls. Positive samples contained low levels of Borrelia-classified reads. Bb-cfDNA is unlikely to become a relevant blood-based diagnostic test for LNB in immunocompetent adults. Borrelia burgdorferi-specific cell-free DNA (Bb-cfDNA) was detected at low levels in plasma from 3/45 patients with Lyme neuroborreliosis and in none of the 16 controls. With medium-depth amplification-free, untargeted metagenomic Nanopore sequencing, plasma microbial cfDNA (mcfDNA) is unlikelyto be clinically useful as a standalone blood-based diagnostic test for Lyme neuroborreliosis.

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Journal
European Journal of Clinical Microbiology & Infectious Diseases
Published
2026-11-06
DOI
https://doi.org/10.1007/s10096-026-05715-x
Primary Topic
Vector-borne infectious diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Borrelia-specific cell-free DNA in plasma from adults with Lyme neuroborreliosis: an explorative study

Helene Mens, Anna Maria Florescu, Marc Stegger, Martin Schou Pedersen et al.
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European Journal of Clinical Microbiology & Infectious Diseases
Vector-borne infectious diseases
article

Borrelia-specific cell-free DNA in plasma from adults with Lyme neuroborreliosis: an explorative study

Helene Mens, Anna Maria Florescu, Marc Stegger, Martin Schou Pedersen, Anne‐Mette Lebech, Lasse Fjordside, Kirsten Ellegaard, Christian Brandt, Christian Stenør, Micha Phill Grønholm Jepsen, Al‐Hasan Hussein Dos
article en

Abstract

Current blood-based diagnostic modalities for LNB have significant limitations. Using Next Generation Sequencing, we investigated blood samples from patients with LNB and non-LNB controls for Borrelia burgdorferi-specific cfDNA (Bb-cfDNA). Blood-samples from 61 adults suspected for LNB were analysed with amplification-free Nanopore metagenomic sequencing and detected cfDNA was cross-referenced with human and Bb-genome databases to identify Bb-specific-cfDNA. Bb-cfDNA was detected in 3 of 45 patients with LNB (6.7%) and in none of the 16 controls. Positive samples contained low levels of Borrelia-classified reads. Bb-cfDNA is unlikely to become a relevant blood-based diagnostic test for LNB in immunocompetent adults. Borrelia burgdorferi-specific cell-free DNA (Bb-cfDNA) was detected at low levels in plasma from 3/45 patients with Lyme neuroborreliosis and in none of the 16 controls. With medium-depth amplification-free, untargeted metagenomic Nanopore sequencing, plasma microbial cfDNA (mcfDNA) is unlikelyto be clinically useful as a standalone blood-based diagnostic test for Lyme neuroborreliosis.

European Journal of Clinical Microbiology & Infectious Diseases
Statens Serum Institut (DK), University of Copenhagen (DK), Murdoch University (AU), Roskilde Sygehus (DK), Herlev Hospital (DK), Copenhagen University Hospital (DK), Gentofte Hospital (DK), Rigshospitalet (DK), Zealand University Hospital (DK), Nordsjællands Hospital (DK), Harry Butler Institute (AU)
Gentofte Hospital, Lundbeckfonden, Rigshospitalet
Good health and well-being
Openalex Percentile: Top 13%
Vector-borne infectious diseases
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