Aminoglycoside Revival: Review of a Historically Important Class of Antimicrobials Undergoing Rejuvenation.

Article Details

Citation

Serio AW, Keepers T, Andrews L, Krause KM

Aminoglycoside Revival: Review of a Historically Important Class of Antimicrobials Undergoing Rejuvenation.

EcoSal Plus. 2018 Nov;8(1). doi: 10.1128/ecosalplus.ESP-0002-2018.

PubMed ID
30447062 [ View in PubMed
]
Abstract

Aminoglycosides are cidal inhibitors of bacterial protein synthesis that have been utilized for the treatment of serious bacterial infections for almost 80 years. There have been approximately 15 members of this class approved worldwide for the treatment of a variety of infections, many serious and life threatening. While aminoglycoside use declined due to the introduction of other antibiotic classes such as cephalosporins, fluoroquinolones, and carbapenems, there has been a resurgence of interest in the class as multidrug-resistant pathogens have spread globally. Furthermore, aminoglycosides are recommended as part of combination therapy for empiric treatment of certain difficult-to-treat infections. The development of semisynthetic aminoglycosides designed to overcome common aminoglycoside resistance mechanisms, and the shift to once-daily dosing, has spurred renewed interest in the class. Plazomicin is the first new aminoglycoside to be approved by the FDA in nearly 40 years, marking the successful start of a new campaign to rejuvenate the class.

DrugBank Data that Cites this Article

Drugs
Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
GentamicinBacterial outer membraneGroupBacteria
Yes
Incorporation into and destabilization
Details
GentamicinCytoplasmic membraneGroupBacteria
Yes
Incorporation into and destabilization
Details
StreptomycinBacterial outer membraneGroupBacteria
Yes
Incorporation into and destabilization
Details
StreptomycinCytoplasmic membraneGroupBacteria
Yes
Incorporation into and destabilization
Details
Tobramycin16S ribosomal RNANucleotideEnteric bacteria and other eubacteria
Yes
Inhibitor
Details
TobramycinBacterial outer membraneGroupBacteria
Yes
Incorporation into and destabilization
Details
TobramycinCytoplasmic membraneGroupBacteria
Yes
Incorporation into and destabilization
Details