4.6 Article

Pathogen infection induces specific transgenerational modifications to gene expression and fitness in Caenorhabditis elegans

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FRONTIERS IN PHYSIOLOGY
卷 14, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fphys.2023.1225858

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epigenetics; transgenerational modification; immunity; C. elegans; pathogen infection; stress response

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The impact of pathogen infection in a parental generation on the response to the same pathogen in future generations through epigenetic modifications has been studied. Using the nematode Caenorhabditis elegans as a model, it was found that training a lineage of C. elegans against a specific pathogen did not significantly change overall survival, but reduced survival variability between generations. Gene expression analysis revealed reduced variation in a specific transcription factor pathway. The study also reported a repeating pattern of survival times in the control lineage, indicating potential regulation of survival variability between generations. In conclusion, pathogen infection can cause specific phenotypic changes through epigenetic modifications, and there may be a system of epigenetic regulation between generations.
How pathogen infection in a parental generation affects response in future generations to the same pathogen via epigenetic modifications has been the topic of recent studies. These studies focused on changes attributed to transgenerational epigenetic inheritance and how these changes cause an observable difference in behavior or immune response in a population. However, we questioned if pathogen infection causes hidden epigenetic changes to fitness that are not observable at the population level. Using the nematode Caenorhabditis elegans as a model organism, we examined the generation-to-generation differences in survival of both an unexposed and primed lineage of animals against a human opportunistic pathogen Salmonella enterica. We discovered that training a lineage of C. elegans against a specific pathogen does not cause a significant change to overall survival, but rather narrows survival variability between generations. Quantification of gene expression revealed reduced variation of a specific member of the TFEB lipophagic pathway. We also provided the first report of a repeating pattern of survival times over the course of 12 generations in the control lineage of C. elegans. This repeating pattern indicates that the variability in survival between generations of the control lineage is not random but may be regulated by unknown mechanisms. Overall, our study indicates that pathogen infection can cause specific phenotypic changes due to epigenetic modifications, and a possible system of epigenetic regulation between generations.

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