Presence of optrA- mediated linezolid resistance in multiple lineages and plasmids of Enterococcus faecalis revealed by long read sequencing
Transferable linezolid resistance due to , , and -like genes is increasingly detected in enterococci associated with animals and humans globally. We aimed to characterize the genetic environment of in linezolid-resistant isolates from Scotland. Six linezolid-resistant isolated from urogenital sample...
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Veröffentlicht in: | Microbiology (Society for General Microbiology) 2022-02, Vol.168 (2) |
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Hauptverfasser: | , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Transferable linezolid resistance due to
,
,
and
-like genes is increasingly detected in enterococci associated with animals and humans globally. We aimed to characterize the genetic environment of
in linezolid-resistant
isolates from Scotland. Six linezolid-resistant
isolated from urogenital samples were confirmed to carry the
gene by PCR. Short read (Illumina) sequencing showed the isolates were genetically distinct (>13900 core SNPs) and belonged to different MLST sequence types. Plasmid contents were examined using hybrid assembly of short and long read (Oxford Nanopore MinION) sequencing technologies. The
gene was located on distinct plasmids in each isolate, suggesting that transfer of a single plasmid did not contribute to
dissemination in this collection. pTM6294-2, BX5936-1 and pWE0438-1 were similar to
-positive plasmids from China and Japan, while the remaining three plasmids had limited similarity to other published examples. We identified the novel Tn
transposon in pWE0254-1 carrying linezolid (
), macrolide (
) and spectinomycin [ANT(9)-Ia] resistance genes. OptrA amino acid sequences differed by 0-20 residues. We report multiple variants of
on distinct plasmids in diverse strains of
. It is important to identify the selection pressures driving the emergence and maintenance of resistance against linezolid to retain the clinical utility of this antibiotic. |
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ISSN: | 1350-0872 1465-2080 |
DOI: | 10.1099/mic.0.001137 |