Evidence map›Paper›PMID 39780098›Full record

ArticleBMC biology2025

Insights into Treponema pallidum genomics from modern and ancient genomes using a novel mapping strategy.

Marta Pla-Díaz, Gülfirde Akgül, Martyna Molak, Louis du Plessis, Hanna Panagiotopoulou, Karolina Doan, Wiesław Bogdanowicz, Paweł Dąbrowski, Maciej Oziembłowski, Barbara Kwiatkowska and 6 more

Abstract read
In one paragraph

Article in BMC biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Formal description ofInternational journal of systematic and evolutionary microbiology · 2026
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4 · The record

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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

16 authors.

Marta Pla-Díaz *Department of Environmental Sciences, University of Basel, Basel, Switzerland.
Gülfirde Akgül *Institute of Evolutionary Medicine, University of Zurich, Zurich, Switzerland.
Martyna MolakCentre of New Technologies, University of Warsaw, Warsaw, Poland.
Louis du PlessisDepartment of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.
Hanna PanagiotopoulouMuseum and Institute of Zoology, Polish Academy of Sciences, Warsaw, Poland.
Karolina DoanMuseum and Institute of Zoology, Polish Academy of Sciences, Warsaw, Poland.
Wiesław BogdanowiczMuseum and Institute of Zoology, Polish Academy of Sciences, Warsaw, Poland.
Paweł DąbrowskiDepartment of Anatomy, Wrocław Medical University, Wrocław, Poland.
Maciej OziembłowskiFaculty of Biotechnology and Food Sciences, Wrocław University of Environmental and Life Sciences, Wrocław, Poland.
Barbara KwiatkowskaDepartment of Anthropology, Wrocław University of Environmental and Life Sciences, Wrocław, Poland.
Jacek SzczurowskiDepartment of Anthropology, Wrocław University of Environmental and Life Sciences, Wrocław, Poland.
Joanna GrzelakDepartment of Anatomy, Wrocław Medical University, Wrocław, Poland.
Natasha AroraZurich Institute of Forensic Medicine, University of Zurich, Zurich, Switzerland.
Kerttu MajanderDepartment of Environmental Sciences, University of Basel, Basel, Switzerland. kerttu.majander@unibas.ch.
Fernando González-CandelasUnidad Mixta Infección y Salud Pública FISABIO, Universidad de Valencia-I2SysBio, Valencia, Spain. fernando.gonzalez@uv.es.
Verena J SchuenemannDepartment of Environmental Sciences, University of Basel, Basel, Switzerland. verena.schuenemann@iem.uzh.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTreponemal diseases are a significant global health risk, presenting challenges to public health and severe consequences to individuals if left untreated. Despite numerous genomic studies on Treponema pallidum and the known possible biases introduced by the choice of the reference genome used for mapping, few investigations have addressed how these biases affect phylogenetic and evolutionary analysis of these bacteria. In this study, we ascertain the importance of selecting an appropriate genomic reference on phylogenetic and evolutionary analyses of T. pallidum.

resultsWe designed a multiple-reference-based (MRB) mapping strategy using four different reference genomes and compared it to traditional single-reference mapping. To conduct this comparison, we created a genomic dataset comprising 77 modern and ancient genomes from the three subspecies of T. pallidum, including a newly sequenced seventeenth century genome (35X mean coverage) of a syphilis-causing strain (designated as W86). Our findings show that recombination detection was consistent across different references, but the choice of reference significantly affected ancient genome reconstruction and phylogenetic inferences. The high-coverage W86 genome introduced in this study also provided a new calibration point for Bayesian molecular clock dating, improving the reconstruction of the evolutionary history of treponemal diseases. Additionally, we identified novel recombination events, positive selection targets, and refined dating estimates for key events in the species' history.

conclusionsThis study highlights the importance of considering methodological implications and reference genome bias in high-throughput sequencing-based whole-genome analysis of T. pallidum, especially of ancient or low-coverage samples, contributing to a deeper understanding of the treponemal pathogen and its subspecies.

Indexed as

Genome, BacterialGenomicsPhylogenyTreponema pallidumHumansBacterial recombinationMapping strategyNatural selectionReference biasReference genome selectionTimescale estimationTreponematoses

Identifiers

PMID39780098
PMCPMC11716147

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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.