Detection of high level aminoglycoside resistance genes among clinical isolates of Enterococcus species
Background Enterococci are intrinsically resistant to clinically achievable concentrations of aminoglycosides. However, high-level resistance to aminoglycosides (HLAR) is primarily due to the acquisition of genes encoding aminoglycoside-modifying enzymes (AMEs). Aminoglycosides along with cell wall...
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Veröffentlicht in: | Egyptian Journal of Medical Human Genetics 2019-11, Vol.20 (1), p.1-6, Article 28 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background
Enterococci are intrinsically resistant to clinically achievable concentrations of aminoglycosides. However, high-level resistance to aminoglycosides (HLAR) is primarily due to the acquisition of genes encoding aminoglycoside-modifying enzymes (AMEs). Aminoglycosides along with cell wall inhibitors are given clinically for treating enterococcal infections. The current study was conducted to investigate the rate of HLAR and to determine aminoglycoside resistance encoding genes profile in enterococcal isolates from different clinical specimens.
Results
From 120
Enterococcus
species, 50 (41.7%) enterococcal isolates were proven to have HLAR, 78% (39/50) have high-level gentamicin resistance (HLGR), and 74% (37/50) were high-level streptomycin-resistant (HLSR). HLGR isolates carried aminoglycoside modifying gene
aac (6′)-Ie-aph (2
′
)-Ia
in 26/39 (66.7%) of isolates, whereas 32/37 (86.5%) of HLSR carried
aph (3
′
)-IIIa
gene and were observed in
E. faecalis
,
E. faecium
,
E. gallinarum
, and
E. casseliflavus
. The
aph (2
′
)-Ib
,
aph (2
′
)-Ic
, and
aph (2
′
)-Id
that encode HLGR could not be detected.
Conclusions
The high detection rate of HLAR among the studied
Enterococcus
species and the coexistence of HLGR and HLSR strains provide crucial insights to the necessity of routine testing for HLAR in the microbiology lab. The main AME genes among HLGR and HLSR enterococci were
aac (6′)-Ie-aph (2″)-Ia
and
aph (3′)-IIIa
, respectively. |
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ISSN: | 2090-2441 1110-8630 2090-2441 |
DOI: | 10.1186/s43042-019-0032-3 |