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Diversity of P1 phage-like elements in multidrug resistant Escherichia coli
The spread of multidrug resistance via mobile genetic elements is a major clinical and veterinary concern. Pathogenic Escherichia coli harbour antibiotic resistance and virulence genes mainly on plasmids, but also bacteriophages and hybrid phage-like plasmids. In this study, the genomes of three E....
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Published in: | Scientific reports 2019-12, Vol.9 (1), p.18861-10, Article 18861 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The spread of multidrug resistance via mobile genetic elements is a major clinical and veterinary concern. Pathogenic
Escherichia coli
harbour antibiotic resistance and virulence genes mainly on plasmids, but also bacteriophages and hybrid phage-like plasmids. In this study, the genomes of three
E. coli
phage-like plasmids, pJIE250-3 from a human
E. coli
clinical isolate, pSvP1 from a porcine ETEC O157 isolate, and pTZ20_1P from a porcine commensal
E. coli
, were sequenced (PacBio RSII), annotated and compared. All three elements are coliphage P1 variants, each with unique adaptations. pJIE250-3 is a P1-derivative that has lost lytic functions and contains no accessory genes. In pTZ20_1P and pSvP1, a core P1-like genome is associated with insertion sequence-mediated acquisition of plasmid modules encoding multidrug resistance and virulence, respectively. The transfer ability of pTZ20_1P, carrying antibiotic resistance markers, was also tested and, although this element was not able to transfer by conjugation, it was able to lysogenize a commensal
E. coli
strain with consequent transfer of resistance. The incidence of P1-like plasmids (~7%) in our
E. coli
collections correlated well with that in public databases. This study highlights the need to investigate the contribution of phage-like plasmids to the successful spread of antibiotic resistant pathotypes. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-019-54895-4 |