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. 2010 Sep-Dec;2(3):291–304. doi: 10.4103/0974-777X.68538

Table 3.

Mechanisms of antibiotic resistance found in Acinetobacter species1,7,54,55

Mechanism of resistance Genetic mechanisms Antimicrobials affected
A. Antimicrobial inactivating (hydrolysing) enzymes
  • Amp C Beta-lactamases [Acinetobacter-derived cephalosporinases (ADCs)]

  • Chromosomal mediated Insertion sequences ISAba1 and IS1135 increase production of beta-lactamase

  • Extended spectrum cephalosporins (including 3rd generation and cephamycin group); cefepime and carbapenems are spared

  • Ambler class D OXA-type enzymes

  • Chromosomal and Plasmid mediated

  • Carbapenems

  • Ambler class B metallo–b-lactamases (MBLs), such as VIM and IMP

  • Mobile genetic elements

  • Carbapenems

  • Ambler class A ESBLs (TEM, SHV)

  • Plasmid, chromosomal or mobile genetic elements

  • All cephalosporins (including 3rd generation) except cephamycin group

B. Reduced access to bacterial targets
  • Altered porin channels and other outer membrane proteins

  • Point mutations

  • Carbapenems

C. Mutations that change targets or cellular functions
  • DNA topoisomerase mutations

  • Point mutations in the bacterial targets gyrA and parC topoisomerase enzymes

  • Quinolones

  • Aminoglycoside-modifying enzyme

  • Plasmid, transposons

  • Aminoglycosides

  • Production of efflux pumps

  • Point mutations

  • Tigecycline, aminoglycosides, quinolones, tetracyclines

  • Modification of cell membrane lipopolysccarides

  • Point mutations

  • Colistin