Phage-plasmid-like elements are found throughout diverse environments and encode niche-specific functional traits

Phage-plasmids are unique mobile genetic elements that function as plasmids and temperate phages. While it has been observed that such elements often encode antibiotic resistance genes and defense system genes, little else is known about other functional traits they encode. Further, no study to date has documented their environmental distribution and prevalence. Here, we performed genome sequence mining of public databases of phages and plasmids utilizing a random forest classifier to identify phage-plasmids. We recovered 5,712 unique phage-plasmid-like genomes from a remarkable array of disparate environments, including human, animal, plant, fungi, soil, sediment, freshwater, wastewater, and saltwater environments. The resulting genomes were used in a comparative sequence analysis, revealing functional traits/accessory genes associated with specific environments. Host-associated elements contained the most defense systems (including CRISPR and anti-CRISPR systems) as well as antibiotic resistance genes, while other environments, such as freshwater and saltwater systems, tended to encode components of various biosynthetic pathways. Interestingly, we identified genes encoding for certain functional traits, including anti-CRISPR systems and specific antibiotic resistance genes, that were enriched in phage-plasmid-like elements relative to both plasmids and phages. Our results highlight that phage-plasmid-like elements are found across a wide-array of environments and likely play a role in shaping microbial ecology in a multitude of niches.

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Publication Details

Journal
PLoS ONE
Published
2026-05-29
DOI
https://doi.org/10.1371/journal.pone.0350027
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Phage-plasmid-like elements are found throughout diverse environments and encode niche-specific functional traits

James I Mullet, Amy Pruden, Liqing Zhang, Connor L. Brown
PLoS ONE
Bacteriophages and microbial interactions
article

Phage-plasmid-like elements are found throughout diverse environments and encode niche-specific functional traits

James I Mullet, Amy Pruden, Liqing Zhang, Connor L. Brown
article en

Abstract

Phage-plasmids are unique mobile genetic elements that function as plasmids and temperate phages. While it has been observed that such elements often encode antibiotic resistance genes and defense system genes, little else is known about other functional traits they encode. Further, no study to date has documented their environmental distribution and prevalence. Here, we performed genome sequence mining of public databases of phages and plasmids utilizing a random forest classifier to identify phage-plasmids. We recovered 5,712 unique phage-plasmid-like genomes from a remarkable array of disparate environments, including human, animal, plant, fungi, soil, sediment, freshwater, wastewater, and saltwater environments. The resulting genomes were used in a comparative sequence analysis, revealing functional traits/accessory genes associated with specific environments. Host-associated elements contained the most defense systems (including CRISPR and anti-CRISPR systems) as well as antibiotic resistance genes, while other environments, such as freshwater and saltwater systems, tended to encode components of various biosynthetic pathways. Interestingly, we identified genes encoding for certain functional traits, including anti-CRISPR systems and specific antibiotic resistance genes, that were enriched in phage-plasmid-like elements relative to both plasmids and phages. Our results highlight that phage-plasmid-like elements are found across a wide-array of environments and likely play a role in shaping microbial ecology in a multitude of niches.

PLoS ONEVol. 21(5)
Massachusetts Institute of Technology (US), Virginia Tech (US), Aalborg University (DK)
National Science Foundation
Clean water and sanitation
Openalex Percentile: Top 6%
Bacteriophages and microbial interactions
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