Target intelligence / Profile preview

Extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-producing Enterobacteriaceae)

Target
ESBL-producing Enterobacteriaceae
Molecular classification
Other (Bacteria; clinical phenotype), If specifically considering the underlying enzyme: Enzyme (beta-lactamase family, Ambler class A and D serine beta-lactamases)
01

Overview

Extended-spectrum beta-lactamase-producing Enterobacteriaceae are Gram-negative bacteria of the Enterobacteriaceae family (such as Escherichia coli and Klebsiella pneumoniae) that produce extended-spectrum beta-lactamase enzymes. These enzymes hydrolyze and inactivate a broad range of beta-lactam antibiotics, including penicillins, third-generation cephalosporins, and aztreonam, leading to significant challenges in the treatment of infections caused by these organisms. The most common enzymes involved are of the TEM, SHV, and CTX-M families, and the genes encoding these enzymes are often plasmid-borne, facilitating rapid horizontal dissemination among bacterial strains. ESBL-producing Enterobacteriaceae are associated with higher rates of morbidity and mortality, especially in hospitalized patients and are recognized as a major global health threat due to their widespread antibiotic resistance.

Other names
ESBL-producing EnterobacteralesESBL-producing Gram-negative bacteriaEnterobacteriaceae producing extended-spectrum beta-lactamasesESBL-E
02

Mechanism of action

Antibiotics typically inhibit bacterial cell wall synthesis (beta-lactams), which is circumvented by ESBLs. Beta-lactamase inhibitors act by inhibiting the enzymatic activity of beta-lactamases (e.g., avibactam, tazobactam), though effectiveness varies by enzyme type. Other antibiotics work via different mechanisms, such as disruption of bacterial membrane potential and function (colistin) or inhibition of protein synthesis (aminoglycosides).

03

Biological functions

Antibiotic resistanceBeta-lactam antibiotic hydrolysisInfection (pathogenesis)
04

Disease associations

Infection (notably complicated urinary tract infections, bloodstream infections, pneumonia, and intra-abdominal infections)Antimicrobial resistance crisis
05

Safety considerations

Limited antibiotic options leading to treatment failureIncreased risk of morbidity and mortality in infected patientsRapid horizontal gene transfer and outbreak potentialUse of last-resort drugs (carbapenems, colistin) can drive additional resistanceNephrotoxicity and neurotoxicity with some last-resort antibiotics
06

Interacting drugs

Carbapenems (imipenem, meropenem, ertapenem)

8 more in the full profile.

07

Biomarkers

Presence of ESBL genes (e.g., bla_TEM, bla_SHV, bla_CTX-M detected by PCR or molecular diagnostics)Resistance phenotype (in vitro resistance to third-generation cephalosporins detected by susceptibility testing)

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