Introduction of epigenetic variation contribute to resistance against the human parasite Schistosoma mansoni

Waddington-type kick-start of adaptive evolution is assumed to be possible based on epigenetic variation alone. We tested this hypothesis in the snail Biomphalaria glabrata, vector of Schistosoma mansoni, the causative agent of the human disease schistosomiasis. Epilines and epigenetic recombinant inbred lines (epiRILs) were used to propagate DNA methylation variants over 3 generations. The fecundity and susceptibility to infection by S. mansoni were measured. Average parasite prevalence has a higher variance in epiRILs than in controls and decreased from 84 ± 5% in controls to 68 ± 21% in epiRILs. The increase in fertility in epiRILs was 12%, with an average heritability of 0.55. The introduction of 1% epimutant offspring snail into resident susceptible populations was simulated by a model. If genetic assimilation of the resistance occurred in 0.3% of the introduced epimutants, susceptibility would be replaced by resistance after less than one hundred generations. Environmental management can therefore be envisaged by introducing epigenetically modified organisms to prevent parasite infections from spreading to the intermediate host and, ultimately, the human population.

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Publication Details

Journal
Epigenetics & Chromatin
Published
2025-07-14
DOI
https://doi.org/10.1186/s13072-025-00607-4
Primary Topic
Parasites and Host Interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Introduction of epigenetic variation contribute to resistance against the human parasite Schistosoma mansoni

Marie Lopez, Benoît Pujol, Cristian Chaparro, Paola B. Arimondo et al.
Epigenetics & Chromatin
Parasites and Host Interactions
article

Introduction of epigenetic variation contribute to resistance against the human parasite Schistosoma mansoni

Marie Lopez, Benoît Pujol, Cristian Chaparro, Paola B. Arimondo, Céline Cosseau, Christoph Grunau, Bart Haegeman, Pierick Mouginot, Nelia Luviano-Aparicio
article en

Abstract

Waddington-type kick-start of adaptive evolution is assumed to be possible based on epigenetic variation alone. We tested this hypothesis in the snail Biomphalaria glabrata, vector of Schistosoma mansoni, the causative agent of the human disease schistosomiasis. Epilines and epigenetic recombinant inbred lines (epiRILs) were used to propagate DNA methylation variants over 3 generations. The fecundity and susceptibility to infection by S. mansoni were measured. Average parasite prevalence has a higher variance in epiRILs than in controls and decreased from 84 ± 5% in controls to 68 ± 21% in epiRILs. The increase in fertility in epiRILs was 12%, with an average heritability of 0.55. The introduction of 1% epimutant offspring snail into resident susceptible populations was simulated by a model. If genetic assimilation of the resistance occurred in 0.3% of the introduced epimutants, susceptibility would be replaced by resistance after less than one hundred generations. Environmental management can therefore be envisaged by introducing epigenetically modified organisms to prevent parasite infections from spreading to the intermediate host and, ultimately, the human population.

Epigenetics & ChromatinVol. 18(1)
Centre National de la Recherche Scientifique (FR), Université de Perpignan (FR), Ifremer (FR), Institut Pasteur (FR), École Pratique des Hautes Études (FR), Pierre Fabre (Germany) (DE), Université de Montpellier (FR), Université Paris Sciences et Lettres (FR), Sorbonne Université (FR), Pierre Fabre (France) (FR), Institut des Biomolécules Max Mousseron (FR), Laboratoire d'Océanographie Microbienne (FR), Chimie Biologique pour le Vivant (FR)
Wellcome Trust, Centre Méditerranéen de l’Environnement et de la Biodiversité, Nederlands Instituut voor Ecologie, Agence Nationale de la Recherche, Koninklijke Nederlandse Akademie van Wetenschappen, Région Occitanie Pyrénées-Méditerranée
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Parasites and Host Interactions
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