Resistance to gentamicin: a growing concern

Insights

Gentamicin and tobramycin resistance in gram-negative bacteria is increasing, with significant percentages of Pseudomonas and Proteus species showing resistance in 1975. This rise necessitates the development of new antimicrobial agents.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Pharmacology

Background:

  • Gentamicin, a broad-spectrum aminoglycoside, was introduced in 1969 for treating aerobic gram-negative bacilli infections.
  • Clinical isolates demonstrating resistance to gentamicin have become increasingly prevalent in recent years.

Purpose of the Study:

  • To document the prevalence of gentamicin and tobramycin resistance in clinical isolates of gram-negative bacilli.
  • To highlight the emergence of resistance in previously uncommon bacterial species.

Main Methods:

  • Laboratory analysis of clinical isolates.
  • In vitro susceptibility testing against gentamicin and tobramycin.

Main Results:

  • In 1975, 32% of Pseudomonas sp and 44% of indole-negative Proteus sp isolates were resistant to gentamicin.
  • Resistance to tobramycin was observed in 24% of Escherichia coli and 28% of indole-negative Proteus sp isolates.
  • Dramatic increase in isolation of gentamicin-resistant Proteus rettgeri and indole-positive Proteus sp.

Conclusions:

  • Rising resistance to gentamicin and tobramycin among gram-negative bacilli is a significant clinical concern.
  • The increasing prevalence of resistant strains necessitates the development of novel antimicrobial therapies.

Related Concept Videos

Antibiotic Selection00:57

Antibiotic Selection

Overview
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations01:15

Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations

Gentamicin, an aminoglycoside antibiotic, is commonly administered via intermittent intravenous infusion to treat severe infections. An intermittent one-hour infusion of gentamicin, administered at eight-hour intervals, allows for precise control of plasma drug concentrations, minimizing toxicity while ensuring therapeutic efficacy. Pharmacokinetic principles govern the dynamics of plasma concentrations and can be mathematically described using specific equations.The plasma drug concentration...
Mechanism of Antibiotic Resistance in MRSA01:25

Mechanism of Antibiotic Resistance in MRSA

Antibiotic resistance in bacteria arises when microorganisms evolve the ability to withstand drugs designed to kill them or inhibit their growth, rendering once-effective treatments useless. This phenomenon, driven by genetic change and selection under antibiotic exposure, poses a profound threat to modern medicine. Mechanisms include drug-inactivating enzymes (e.g., β-lactamases), efflux pumps that eject antibiotics, mutations altering antibiotic targets, decreased drug uptake, and acquisition...
Clinical Significance of Antibiotic Resistance01:25

Clinical Significance of Antibiotic Resistance

Methicillin-resistant Staphylococcus aureus (MRSA) presents a critical public health threat, arising from its capacity to resist β-lactam antibiotics due to acquisition of the mecA gene within the staphylococcal cassette chromosome mec (SCCmec). This gene encodes penicillin-binding protein 2a (PBP2a), which impairs binding efficacy of methicillin and other β-lactams. MRSA has evolved into distinct clonal lineages impacting humans and animals alike, reinforcing its significance within the One...