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<p>Torque Teno Virus (TTV) is a widespread commensal virus within the human virome, characterized by a high prevalence in human population and an unclear pathogenic role. Over the past three decades, TTV has garnered increasing attention due to its ability to establish lifelong chronic viremia, which intriguingly fluctuates among individuals in relation to immune competence status, with a typical peak after an organ transplantation, followed by a plateau and a slow decrease. The regulatory mechanisms underlying TTV infection remain elusive, and factors influencing its interactions with the immune system have yet to be identified. To explore this complex interplay, we analyzed DNA methylation patterns associated with TTV load in older adult hospitalized patients (mean age: 83.15 ± 7.49) from the PROMOTERA cohort. In this study, we present for the first time the identification of differentially methylated probes (DMPs) correlated to TTV load in our cohort. The statistically significant DMPs were located in genes involved in immune regulation and lipid metabolism. To further characterize these findings, we performed an exploratory enrichment analysis by applying several <i>p</i>-value thresholds, which yielded multiple gene lists derived from the sets of significant probes. Genes associated with this epigenetic signature were found to enrich functional pathways related to immune activation, leukocyte differentiation, and cytokine production, while additional significantly enriched gene sets were involved in cell–cell adhesion and cell migration processes. Since our analysis followed an exploratory approach, these results should be interpreted as hypothesis-generating and warrant further investigation.</p> Graphical Abstract <p></p>

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Methylation patterns associated with TTV load in geriatric hospitalized patients: an exploratory functional analysis

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年10月22日

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  • Carlo Fortunato,
  • Pietro Giorgio Spezia,
  • Federica Novazzi,
  • Gretta Veronica Badillo Pazmay,
  • Laura Cianfruglia,
  • Francesca Drago Ferrante,
  • Davide Gentilini,
  • Luciano Calzari,
  • Paolo Antonio Grossi,
  • Nicasio Mancini,
  • Luigi Rosa,
  • Mirko Di Rosa,
  • Anna Rita Bonfigli,
  • Roberta Galeazzi,
  • Antonio Cherubini,
  • Leonardo Biscetti,
  • Riccardo Sarzani,
  • Fabrizia Lattanzio,
  • Maurizio Cardelli,
  • Fabiola Olivieri,
  • Marco Malavolta,
  • Francesco Piacenza,
  • Fabrizio Maggi,
  • Robertina Giacconi

摘要

Torque Teno Virus (TTV) is a widespread commensal virus within the human virome, characterized by a high prevalence in human population and an unclear pathogenic role. Over the past three decades, TTV has garnered increasing attention due to its ability to establish lifelong chronic viremia, which intriguingly fluctuates among individuals in relation to immune competence status, with a typical peak after an organ transplantation, followed by a plateau and a slow decrease. The regulatory mechanisms underlying TTV infection remain elusive, and factors influencing its interactions with the immune system have yet to be identified. To explore this complex interplay, we analyzed DNA methylation patterns associated with TTV load in older adult hospitalized patients (mean age: 83.15 ± 7.49) from the PROMOTERA cohort. In this study, we present for the first time the identification of differentially methylated probes (DMPs) correlated to TTV load in our cohort. The statistically significant DMPs were located in genes involved in immune regulation and lipid metabolism. To further characterize these findings, we performed an exploratory enrichment analysis by applying several p-value thresholds, which yielded multiple gene lists derived from the sets of significant probes. Genes associated with this epigenetic signature were found to enrich functional pathways related to immune activation, leukocyte differentiation, and cytokine production, while additional significantly enriched gene sets were involved in cell–cell adhesion and cell migration processes. Since our analysis followed an exploratory approach, these results should be interpreted as hypothesis-generating and warrant further investigation.

Graphical Abstract