Host-encoded DNA methyltransferases modify the epigenome and host tropism of invading phages

Restriction modification (RM) systems are ubiquitous bacterial defense systems; however, some phages evade RM system and adapt to their bacterial hosts. In such cases, phages are thought to stochastically acquire DNA methylation from host-encoded DNA methyltransferases (MTases), facilitating host adaptation. However, no studies have directly compared the methylomes of host bacteria and their infecting phages. Here, we demonstrate the epigenetic landscape of adapted phages with diverse infection histories, focusing on the broad host-range phage KHP30T as its adapts to three <i>Helicobacter pylori</i> strains. Using a multistage infection system, we observed that the adapted phages displayed significantly high titers against the last infected <i>H. pylori</i> strain, suggesting an attendant change in host tropism. Single-molecule real-time sequencing revealed that methylated motifs were predominantly shared between the adapted phages and their most recent host. Our findings enhance our understanding of epigenetic phage-host interactions, which have significant implications for microbial ecology.

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Publication Details

Journal
iScience
Published
2025-03-22
DOI
https://doi.org/10.1016/j.isci.2025.112264
Citations
6
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
10.30

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article

Host-encoded DNA methyltransferases modify the epigenome and host tropism of invading phages

Michiko Takahashi, Shigenobu Matsuzaki, Hiroaki Takeuchi, Yuki Matsumoto et al.
6 citations
iScience
Bacteriophages and microbial interactions
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article

Host-encoded DNA methyltransferases modify the epigenome and host tropism of invading phages

Michiko Takahashi, Shigenobu Matsuzaki, Hiroaki Takeuchi, Yuki Matsumoto, Hiromichi Maeda, Takako Ujihara, Satoru Seo, Satoshi Hiraoka, Keizo Nagasaki, Rikako Shibagaki
article en
6 citations

Abstract

Restriction modification (RM) systems are ubiquitous bacterial defense systems; however, some phages evade RM system and adapt to their bacterial hosts. In such cases, phages are thought to stochastically acquire DNA methylation from host-encoded DNA methyltransferases (MTases), facilitating host adaptation. However, no studies have directly compared the methylomes of host bacteria and their infecting phages. Here, we demonstrate the epigenetic landscape of adapted phages with diverse infection histories, focusing on the broad host-range phage KHP30T as its adapts to three <i>Helicobacter pylori</i> strains. Using a multistage infection system, we observed that the adapted phages displayed significantly high titers against the last infected <i>H. pylori</i> strain, suggesting an attendant change in host tropism. Single-molecule real-time sequencing revealed that methylated motifs were predominantly shared between the adapted phages and their most recent host. Our findings enhance our understanding of epigenetic phage-host interactions, which have significant implications for microbial ecology.

iScienceVol. 28(4)
Japan Agency for Marine-Earth Science and Technology (JP), Kōchi University (JP), International University of Health and Welfare (JP), Kochi Gakuen College (JP)
Kochi University, Japan Society for the Promotion of Science, Japan Science and Technology Agency, Precursory Research for Embryonic Science and Technology, Exploratory Research for Advanced Technology, ACT-X
Zero hunger
Openalex Percentile: Top 2%
Bacteriophages and microbial interactions
10.30
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