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

J James I. Mullet L Liqing Zhang A Amy Pruden C Connor L. Brown

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.

Article Details

Journal PLoS ONE
Volume / Issue Vol. 21, Issue 5
Published May 29, 2026
Pages e0350027
ISSN 1932-6203
Publisher Public Library of Science

Journal Info

PLoS ONE

Public Library of Science

ISSN: 1932-6203 Open Access Health Sciences

Authors (4)

J

James I. Mullet

L

Liqing Zhang

A

Amy Pruden

C

Connor L. Brown