Cited by 5Bacteriophages and microbial interactionsMicrobial Community Ecology and PhysiologyMicrobial metabolism and enzyme function

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Parasitic connections: a patescibacterial epibiont, its methylotrophic gammaproteobacterial host, and their phages

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Bouderka, Feriel, López-García, Purificación, Deschamps, Philippe, Zhou, Yifan, Krupovic, Mart, Gutiérrez-Preciado, Ana, Ciobanu, Maria, Bertolino, Paola, David, Gwendoline, Moreira, David, Jardillier, Ludwig·2026·mBio

Published version of a preprint

Abstract

Patescibacteriota form a very diverse and widely distributed phylum of small bacteria inferred to have an episymbiotic lifestyle. However, the prevalence of this lifestyle within the phylum and its host specificity remain poorly known due to the scarcity of cultured representatives. Here, we describe a complex system consisting of a patescibacterium, its gammaproteobacterial hosts, and their respective phages based on enrichment cultures and metagenomic data from two shallow, geographically close, freshwater ecosystems. The patescibacterium Strigamonas methylophilicida sp. nov. defines a new genus within the family Absconditicoccaceae. It grows as an epibiont on cells of methanotrophic species of the gammaproteobacterial family Methylophilaceae. Strigamonas cells grow tightly attached to the host, sometimes forming stacks that connect two host cells. Despite a surprisingly large genome (1.9 Mb) compared to many other Patescibacteriota, S. methylophilicida lacks many essential biosynthetic pathways, including the complete biosynthesis of phospholipids, amino acids, and nucleic acids, implying a dependence on the host to obtain these molecules. We also identified and assembled the complete genomes of one patescibacterial phage that might represent a new virus family within the class Caudoviricetes , and two Methylophilaceae phages predicted to have head-tailed and filamentous virions, respectively. The patesciphage uses a modified genetic code similar to that of its host and encodes four tRNA genes, including the suppressor tRNA gene for the UGA stop codon, which is reassigned to glycine in many Patescibacteriota. Our results confirm a prevalent episymbiotic lifestyle in Absconditicoccaceae and further suggest a clade-specific adaptation of this patescibacterial family for gammaproteobacterial hosts. IMPORTANCE: Patescibacteriota are ultra-small bacteria with reduced genomes that rely on symbiotic interactions with other prokaryotes; however, their host specificity and associated viral parasites remain poorly characterized due to limited cultured representatives. By combining targeted cultivation with genomic and microscopy analyses, we reveal previously unrecognized host lineages and expand the known viral diversity infecting this major, but still poorly known, bacterial phylum. We describe Strigamonas methylophilicida , a new patescibacterial species of the family Absconditicoccaceae that grows as an epibiont on various methylotrophic Gammaproteobacteria. This expands the host range for this family, previously found to infect only photosynthetic partners. Using enrichment cultures and metagenomics, we retrieved complete genomes of novel phages infecting S. methylophilicida and its methylotrophic hosts, including one phage that uses a modified genetic code matching that of the patescibacterium, which shows a specific viral adaptation to infect Absconditicoccaceae hosts. Our findings reveal a previously unrecognized patescibacteria-methylotrophs-phages tripartite interaction in freshwater environments, highlight the adaptations of patescibacterial phages, and shed light on the complex ecology and evolution of host-parasite-phage dynamics in understudied bacterial lineages.

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Metadata

Authors
Bouderka, F., López-García, P., Deschamps, P., Zhou, Y., Krupovic, M., Gutiérrez-Preciado, A., Ciobanu, M., Bertolino, P., David, G., Moreira, D., & Jardillier, L.
Affiliations
  • Centre National de la Recherche Scientifique (FR)
  • Unité d'Ecologie Société et Evolution, CNRS, Université Paris-Saclay, AgroParisTech
  • Institut Pasteur, Université Paris Cité, CNRS UMR 6047, Cell Biology and Virology of Archaea Unit
Corresponding author
  • Moreira, David
  • Jardillier, Ludwig
Venue
mBio
Published
2026-04-08
Volume
17
Issue
4
Pages
e0002526-e0002526
ISSN
2150-7511 (ISSN-L)
OpenAlex
W7134961109
Cited by
5
References
3
Citations by year
2026: 2
FWCI
6.94
Type
journal article
Language
en
Open access
Locations
  • mBio (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • HAL (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • H2020 European Research Council (787904)
  • HORIZON EUROPE European Research Council (101141745)
  • Agence Nationale de la Recherche (ANR-22-CE02-0012-02, ANR-23-CE02-0016-01)
Topics
  • Life Sciences › Immunology and Microbiology › Virology › Bacteriophages and microbial interactions
  • Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial metabolism and enzyme function
Keywords
Methylophilaceae, epibionts, host specificity, bacterial phages, Caudoviricetes, filamentous phage, suppressor tRNA, reduced genome, freshwater bacteria, new genus and species, viral diversity, host-virus interaction, methanotrophic bacteria, methylotrophic bacteria
MeSH terms
Bacteriophages, Fresh Water, Phylogeny, Symbiosis, Sequence Analysis, DNA, Gammaproteobacteria, Host Specificity

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