Evidence map›Paper›PMID 42102105›Full record

ArticlePloS one2026

The wild, wild west of plasmids: First insights into comparative genomics of Borrelia burgdorferi sensu lato.

Sabrina Hepner, Robert E Rollins, Evangelos Mourkas, Konstantin Kuleshov, Sherwood Casjens, Weigang Qiu, Alexandra Dangel, Dunia Velázquez, Sergey Y Kovalev, Andreas Wieser and 4 more

Abstract readComparative Study
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Sabrina HepnerGerman National Reference Centre for Borrelia, Oberschleissheim, Germany.ORCID https://orcid.org/0009-0000-7768-4867
Robert E RollinsInstitute of Avian Research "Vogelwarte Helgoland", Wilhelmshaven, Germany.ORCID https://orcid.org/0000-0002-5779-7001
Evangelos MourkasZoonosis Science Centre, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0002-7411-4743
Konstantin KuleshovCentral Research Institute of Epidemiology, Moscow, Russia.
Sherwood CasjensSchool of Biological Sciences and Division of Microbiology and Immunology, Pathology Department, University of Utah School, Utah, United States of America.
Weigang QiuGraduate Center and Hunter College, City University of New York, New York, United States of America.
Alexandra DangelBavarian Health and Food Safety Authority, Oberschleissheim, Germany.
Dunia VelázquezGerman National Reference Centre for Borrelia, Oberschleissheim, Germany.
Sergey Y KovalevInstitute of Natural Science and Mathematics, Ural Federal University, Yekaterinburg, Russia.ORCID https://orcid.org/0000-0002-4669-5288
Andreas WieserMedical Microbiology and Hospital Epidemiology, Max von Pettenkofer Institute, Faculty of Medicine, LMU Munich, Munich, Germany.
Johannes HübnerDr. von Hauner Children's Hospital, LMU Munich, Munich, Germany.
Andreas SingGerman National Reference Centre for Borrelia, Oberschleissheim, Germany.
Volker FingerleGerman National Reference Centre for Borrelia, Oberschleissheim, Germany.
Gabriele MargosGerman National Reference Centre for Borrelia, Oberschleissheim, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lyme borreliosis is caused by species of the Borrelia burgdorferi sensu lato complex. Genospecies vary in human pathogenicity, reservoir host and tick vector adaptation. What causes these differences is currently unknown, but some answers are likely to be found within the fragmented genomes containing linear and circular plasmids (and even fusions). These plasmids are highly variable and challenging to reconstruct completely. We aimed to analyze plasmid presence/absence and to identify trends in plasmid numbers and/or types associated with specific ecological adaptations or pathogenic potentials. For this, we used the most complete, reliable, and currently available 86 B. burgdorferi s.l. genomes (30 newly sequenced, 56 publicly available) belonging to 21 of the 28 known species. The plasmid types per isolate vary from 6-21 (median: 12) and linear plasmid numbers (3-12, median: 7) are significantly higher than circular plasmids (2-11, median: 5). The only plasmids found in all isolates are lp54 and cp26 and only a few species- or population-specific plasmids are identified, demonstrating the high variability. Species with smaller plasmid counts (median < 11) tend to have fewer lp28 and cp32 plasmids than larger plasmid counts species (median ≥ 15). Significantly higher total and circular plasmid numbers are found in rodents-only compared to birds-only associated species. Interestingly, plasmid numbers are not significantly reduced in species associated with a single reservoir host/vector compared to multiple. Analyses of the plasmid-location of the vls/vlsE antigenic variation system highlighted the dynamic nature of B. burgdorferi s.l. plasmids. Surprisingly, whilst the plasmid repertoire of B. burgdorferi s.l. is very plastic and variable, our analyses rarely reveal plasmids associated with specific ecological adaptations or pathogenic potentials. However, some plasmids were more frequently found in one of the groups and will be of interest for gene-based analyses that will be required for further progress in this research area.

Indexed as

Borrelia burgdorferiBorrelia burgdorferi GroupGenomicsPlasmidsAnimalsGenome, BacterialHumansLyme DiseasePhylogeny

Identifiers

PMID42102105
PMCPMC13155636

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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.