High Carbapenem Resistance Caused by VIM and NDM Enzymes and OprD Alteration in Nonfermenter Bacteria Isolated from a Libyan Hospital
Acinetobacter baumannii and Pseudomonas aeruginosa are among the most prevalent pathogens causing a wide range of serious infections in hospitalized patients and contaminating intensive care units and inanimate surfaces. The purpose of this study was to investigate the mechanism of carbapenem resist...
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Veröffentlicht in: | Microbial drug resistance (Larchmont, N.Y.) N.Y.), 2021-11, Vol.27 (11), p.1546-1554 |
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Sprache: | eng |
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Zusammenfassung: | Acinetobacter baumannii
and
Pseudomonas aeruginosa
are among the most prevalent pathogens causing a wide range of serious infections in hospitalized patients and contaminating intensive care units and inanimate surfaces. The purpose of this study was to investigate the mechanism of carbapenem resistance in clinical and hospital environmental isolates of
A. baumannii
and
P. aeruginosa
recovered from a Libyan hospital. From a total of 82 Gram-negative bacteria, 8 isolates of
A. baumannii
and 3 isolates of
P. aeruginosa
exhibited resistance to imipenem with minimum inhibitory concentrations ranging from 16 to >32 μg/mL. Five isolates of
A. baumannii
harbored
bla
OXA-23
gene, from which three isolates were collected from patients and two from hospital environment. Only one isolate harbored
bla
NDM-1
gene, which was responsible for carbapenem resistance in
A. baumannii
. The
OprD
gene seems to be disturbed by an insertion sequence (
IS
) in two isolates and affected by polymorphism in one isolate. Pulsed-field gel electrophoresis results showed high genetic diversity among carbapenemase producing
A. baumannii
. This study highlights the dissemination of
bla
OXA-23
and
bla
NDM-1
genes in a Libyan setting. Therefore, infection prevention and control practices, antimicrobial stewardship initiatives, and antimicrobial resistance surveillance systems should be implemented to prevent the wide spread of antimicrobial resistance. |
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ISSN: | 1076-6294 1931-8448 |
DOI: | 10.1089/mdr.2020.0175 |