The Antimicrobial Resistance Characteristics of Imipenem-Non-Susceptible, Imipenemase-6-Producing <i>Escherichia coli</i>

Imipenemase-6 (IMP-6) type carbapenemase-producing <i>Enterobacteriaceae</i> is regarded as dangerous due to its unique lack of antimicrobial susceptibility. It is resistant to meropenem (MEPM) but susceptible to imipenem (IPM). In addition to carbapenemase, outer membrane porins and eff...

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Main Authors: Reo Onishi, Katsumi Shigemura, Kayo Osawa, Young-Min Yang, Koki Maeda, Shiuh-Bin Fang, Shian-Ying Sung, Kenichiro Onuma, Atsushi Uda, Takayuki Miyara, Masato Fujisawa
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:Antibiotics
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Online Access:https://www.mdpi.com/2079-6382/11/1/32
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Summary:Imipenemase-6 (IMP-6) type carbapenemase-producing <i>Enterobacteriaceae</i> is regarded as dangerous due to its unique lack of antimicrobial susceptibility. It is resistant to meropenem (MEPM) but susceptible to imipenem (IPM). In addition to carbapenemase, outer membrane porins and efflux pumps also play roles in carbapenem resistance by reducing the antimicrobial concentration inside cells. Extended-spectrum β-lactamase (ESBL) is transmitted with IMP-6 by the plasmid and broadens the spectrum of antimicrobial resistance. We collected 42 strains of IMP-6-producing <i>Escherichia coli</i> and conducted a molecular analysis of carbapenemase, ESBL, porin, efflux, and epidemiological characteristics using plasmid replicon typing. Among the 42 isolates, 21 strains were susceptible to IPM (50.0%) and 1 (2.4%) to MEPM. Seventeen strains (40.5%) co-produced CTX-M-2 type ESBL. We found that the relative expression of <i>ompC</i> and <i>ompF</i> significantly correlated with the MIC of IPM (<i>p</i> = 0.01 and <i>p</i> = 0.03, respectively). Sixty-eight% of CTX-M-2-non-producing strains had IncI1, which was significantly different from CTX-M-2-producing strains (<i>p</i> < 0.001). In conclusion, 50.0% of our IMP-6-producing strains were non-susceptible to IPM, which is different from the typical pattern and can be attributed to decreased porin expression. Further studies investigating other types of carbapenemase are warranted.
ISSN:2079-6382