Identification of fosA10 , a Novel Plasmid-Mediated Fosfomycin Resistance Gene of Klebsiella pneumoniae Origin, in Escherichia coli
Several subtypes of plasmid-mediated fosfomycin resistance gene in have been reported worldwide and have caused concern. The present study characterized a novel member of gene located on a plasmid from . A fosfomycin-resistant isolate PK9 was recovered from a chicken meat sample in 2018. The presenc...
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Veröffentlicht in: | Infection and drug resistance 2020-05, Vol.13, p.1273-1279 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Several subtypes of plasmid-mediated fosfomycin resistance gene
in
have been reported worldwide and have caused concern. The present study characterized a novel member of
gene located on a plasmid from
.
A fosfomycin-resistant
isolate PK9 was recovered from a chicken meat sample in 2018. The presence of
genes was detected by PCR and sequencing. Whole-genome sequencing (WGS), conjugation, and cloning were performed to identify the mechanism responsible for fosfomycin resistance. Oxford Nanopore MinION sequencing was carried out to characterize the plasmid carrying fosfomycin resistance gene and the genetic context of the novel
variant.
A novel
gene with significant homology (>98%) with
and
genes was identified by WGS and was named
. FosA10 shared 56.1% to 98.6% amino acid sequence identity with other reported plasmid-mediated FosA enzymes. Fosfomycin resistance and
gene were successfully transferred to
C600 by conjugation. Cloning confirmed that FosA10 could confer fosfomycin resistance (MIC > 128 μg/mL). The
gene was localized on a 53kb IncFII (F35:A-:B-) plasmid. The
fragment (4328 bp), located between two copies of IS10R, showed 100% identity with the chromosomal sequences of 17
strains of ST664 and one of ST3821 in GenBank.
Our findings indicated that the
gene of
might be captured from the chromosome of
by IS
, which further demonstrated that
might act as a reservoir of
-like genes acquired by
. |
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ISSN: | 1178-6973 1178-6973 |
DOI: | 10.2147/IDR.S251360 |