
About
Beside the study of the biology of HSV-1, one of the main focus of the team is to understand, at the molecular level and using HSV-1 as a model, some basic aspects of nuclear and chromatin dynamics related to the maintenance of genome integrity and to the regulation of gene expression.
The major research interests of the team LOMONTE are:
- The study of the pathological consequences of the infection of neurons from the peripheral and central nervous systems by the neurotropic virus herpes simplex virus 1 (HSV-1). We essentially focus our research on the establishment of latency and reactivation processes.
- The study of the implication of nuclear architecture, especially promyelocytic leukemia nuclear bodies (PML NBs), in the regulation of latent HSV-1 chromatin features and in chromatin dynamics during the process of senescence.
- The study of the chromatin alterations associated to damage or to genetic pathologies, and potentially linked to genetic instabilities, or motoneurons decay.
Members

Patrick Lomonte
Senior Researcher

Tristan Bargain
PHD STUDENT

Damien Blanc
Student

Lucas Bonnefoy
Student

Pierre-Adrien Buffoni
Clinical Assistant Professor

Callum Burnard
MCU

Armelle Corpet
Associate Professor

Mazarine Couturier
PHD STUDENT

Tristan Escure
Doctorant

Clémence Guerriau
Research Assistant

Franceline Juillard
Assistant Professor

Rémi Lebon
PHD STUDENT

Alicia Lopes
Student

Chloé Madras
Research Assistant

Karine Monier
Research Engineer

Rémi Neplaz
PHD STUDENT

Delphine Poncet
Professor
Publications
2025
Functional analysis of telomere maintenance mechanisms is more informative than immunohistochemistry for ATRX mutation interpretation in Gliomas.,
Acta Neuropathol Commun 2025 Dec; 14(1): 25.
2025
A p97-PML NBs axis is essential for chromatin-bound cGAS untethering and degradation upon senescence-prone DNA damage,
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2025
Centromeric DNA amplification triggered by viral proteins activates nuclear cGAS.,
Cell 2025 Jul; 188(15): 4043-4057.e21.
2025
[Lyon, at the center of the global virology research challenge].,
Virologie (Montrouge) 2025 Apr; 29(2): 59-63.
2025
Correlation-Based Nanometric Localization Using Lattice SIM² and dSTORM in PML Nuclear Bodies validated by Calibration Spheres,
Biochem Biophys Res Commun 2025 Mar; 752(): 151450.
2024
The HUSH epigenetic repressor complex silences PML nuclear body- associated HSV-1 quiescent genomes,
Proc Natl Acad Sci U S A 2024 Dec; 121(49): e2412258121.
2023
Nucleolar reorganization after cellular stress is orchestrated by SMN shuttling between nuclear compartments.,
Nat Commun 2023 Nov; 14(1): 7384.
2023
The TUDOR domain of SMN is an H3K79 me1 histone mark reader,
Life Sci Alliance 2023 Jun; 6(6): .
2023
Interplay between PML NBs and HIRA for H3.3 dynamics following type I interferon stimulus,
Elife 2023 May; 12(): .
2023
The HUSH-SETDB1-MORC2 epigenetic repressor complex restricts herpesvirus infection in association with PML nuclear bodies,
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2022
Initial TK-deficient HSV-1 infection in the lip alters contralateral lip challenge immune dynamics,
Sci Rep 2022 May; 12(1): 8489.
2022
SMA-linked SMN mutants prevent phase separation properties and SMN interactions with FMRP family members,
Life Science Alliance.
2022
Microrchidia CW-Type Zinc Finger 2, a Chromatin Modifier in a Spectrum of Peripheral Neuropathies,
Front Cell Neurosci 2022 ; 16(): 896854.
2020
Latent/Quiescent Herpes Simplex Virus 1 Genome Detection by Fluorescence In Situ Hybridization (FISH),
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