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Monobactam
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Aztreonam
Drug class
Aztreonam. (The four-membered ring at the bottom is the β-lactam. There is a second thiazole ring, but it is not fused to the β-lactam ring.)
Class identifiers
UseBacterial infection
ATC codeJ01DF
External links
MeSHD008997
Legal status
In Wikidata
Tigemonam

Monobactams are bacterially-produced monocyclic β-lactam antibiotics. The β-lactam ring is not fused to another ring, in contrast to most other β-lactams.[1]

Monobactams are narrow-spectrum antibiotics[2] effective only against (strictly or facultatively[3]) aerobic Gram-negative bacilli,[4][5][3] exhibiting a high level of resistance to beta-lactamases of these organisms.[3] Due to their narrow spectrum, monobactams can be used to treat infections by susceptible bacteria without disrupting the patient's microbiota.[2] Monobactams are nevertheless seldom used.[2]

Aztreonam is the archetypal monobactam.[6] Other monobactams include tigemonam,[7] nocardicin A, carumonam and tabtoxin. An example of a monobactam that lacks antibiotic activity, but is used clinically for other purposes, is the cholesterol absorption inhibitor ezetimibe which is used to treat hypercholesterolemia.[8]

Pharmacology

[edit]

Monobactams exert their antibacterial effects by binding to penicillin-binding proteins (PBPs), thereby inhibiting bacterial wall synthesis.[5] Monobactams exhibit poor affinity for PBPs of Gram-positive bacteria as well as of strictly anaerobic bacteria, resulting in a lack of significant antimicrobial activity against these kinds of organisms.[3] Monobactams are synergetic with aminoglycosides, and piperacillin.[5]

Bacterial resistance to monobactams have been observed, and is mediated by bacterial beta-lactamases.[5]

Adverse effects

[edit]

Adverse effects to monobactams can include skin rash and occasional abnormal liver functions.[citation needed]

Monobactam antibiotics exhibit no IgE cross-reactivity reactions with penicillin but have shown some cross reactivity with cephalosporins, most notably ceftazidime, which contains an identical side chain as aztreonam.[9] Monobactams can trigger seizures in patients with history of seizures, although the risk is lower than with penicillins.[citation needed]

Research

[edit]

Siderophore-conjugated monobactams show promise for the treatment of multi drug-resistant pathogens.[10]

References

[edit]
[edit]
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Monobactam

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Monobactams are a class of synthetic beta-lactam antibiotics featuring a monocyclic beta-lactam ring structure, which sets them apart from the bicyclic structures of penicillins, cephalosporins, and carbapenems. This unique architecture confers resistance to many beta-lactamases produced by Gram-negative bacteria, making monobactams particularly effective against aerobic Gram-negative pathogens such as Pseudomonas aeruginosa, Escherichia coli, and Klebsiella species. The prototype and only monobactam in widespread clinical use is aztreonam, a bactericidal agent that inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), primarily PBP3, leading to cell lysis and death. Originally isolated from the bacterium in the late 1970s, natural monobactams exhibited limited antibacterial activity, prompting the development of synthetic derivatives like , which was approved by the in 1986 for parenteral administration. demonstrates a narrow spectrum of activity, with no significant efficacy against , anaerobes, or most atypical pathogens, resembling the profile of aminoglycosides but without the associated or . It is primarily indicated for treating moderate-to-severe infections, including urinary tract infections, lower respiratory tract infections, intra-abdominal infections, septicemia, and skin and skin-structure infections caused by susceptible Gram-negative aerobes. In patients with , inhaled (as Cayston) is used to suppress chronic P. aeruginosa colonization in those aged 6 years and older. Monobactams are generally well-tolerated, with a low incidence of hypersensitivity reactions and minimal cross-reactivity in patients allergic to other beta-lactams, due to their distinct immunogenic epitopes. Common adverse effects include gastrointestinal upset, rash, and injection-site reactions, while rare hepatotoxicity manifests as asymptomatic elevations in serum aminotransferases in 10% to 38% of recipients. Aztreonam is renally excreted with a half-life of approximately 1.7 hours in individuals with normal kidney function, necessitating dose adjustments in renal impairment. In February 2025, the FDA approved aztreonam in combination with avibactam (Emblaveo) for the treatment of complicated intra-abdominal infections caused by multidrug-resistant Gram-negative bacteria in adults with limited treatment options. Ongoing research explores novel monobactams to combat multidrug-resistant Gram-negative infections, leveraging the scaffold's stability against extended-spectrum beta-lactamases.

Chemistry

Structure

Monobactams are a class of synthetic or semi-synthetic β-lactam antibiotics characterized by a single monocyclic β-lactam ring, without the fused ring systems found in other β-lactams such as penicillins or cephalosporins. This distinguishes them structurally from bicyclic β-lactams, where the β-lactam ring is fused to a five- or six-membered ring, altering their overall conformation and enzymatic interactions. The core structure of monobactams consists of an azetidinone ring—a four-membered β-lactam cycle featuring a carbonyl group between the nitrogen and carbon atoms—typically substituted with side chains at positions 1 (on the nitrogen), 3 (on the carbon adjacent to the carbonyl), and 4 (the carbon opposite the nitrogen). These substitutions modulate their antibacterial potency and pharmacokinetic properties; for instance, a sulfonic acid group is often present at position 1, directly attached to the ring nitrogen, replacing the carboxylate seen in other β-lactams. A representative example is aztreonam, which bears a sulfonic acid at C-1 and an aminothiazole-oxime side chain at C-3, specifically a (Z)-2-(2-aminothiazol-4-yl)-2-[(2-methyl-1-carboxypropoxy)imino]acetyl group, along with a methyl substituent at C-4. Naturally occurring monobactams, such as nocardicins from Nocardia uniformis and sulfazecin from Pseudomonas species or Gluconobacter, have been isolated from soil bacteria, demonstrating the class's origins in microbial secondary metabolism. However, clinically used monobactams like aztreonam are primarily synthetic derivatives optimized for therapeutic efficacy. The absence of a fused in monobactams confers advantages in stability against many β-lactamases, as these enzymes often recognize and hydrolyze the bicyclic scaffolds of penicillins and cephalosporins more effectively. This monocyclic architecture results in a more planar β-lactam and reduced steric hindrance, enhancing resistance to by serine-based β-lactamases while maintaining the high (due to the 90° bond angles in the four-membered ring) that drives reactivity with . In comparison, the fused rings in other β-lactams increase overall strain but also provide binding epitopes for β-lactamases, leading to greater susceptibility.

Synthesis

The synthesis of monobactams has historically faced challenges in developing stereoselective methods for constructing the strained β-lactam ring while incorporating the critical N-sulfonic acid functionality. Early approaches adapted the Staudinger [2+2] cycloaddition reaction, involving the reaction of a derived from a and an , to form the azetidinone core of monobactams. However, achieving high at the C-3 and C-4 positions proved difficult, as the reaction often favors trans geometry due to steric and electronic factors in the , necessitating chiral auxiliaries or asymmetric variants to control the absolute of the biologically active trans isomers required for antibacterial activity. A pivotal synthetic route for , the prototypical monobactam, employs a stepwise assembly beginning with β-amino acids derived from L-threonine to establish the chiral centers at C-3 and C-4. The process involves forming the azetidinone ring via cyclization, followed by protection of the group—often as a or salt—to avoid interference during subsequent steps, and culminates in amide coupling of the (Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetic acid side chain using activating agents like dicyclohexylcarbodiimide or phosphorus-based reagents. This efficient, multi-step protocol was pioneered by & Sons in the early 1980s and patented for industrial scalability, yielding in high purity suitable for clinical use. Semi-synthetic strategies leverage natural monobactams obtained from bacterial , such as SQ 26,180 isolated from , as starting scaffolds. These precursors undergo targeted chemical derivatization, including selective at the C-3 amino position with acyl chlorides or activated carboxylic acids and adjustment of the N-1 substituent to improve pharmacokinetic properties, thereby generating analogs with enhanced potency against Gram-negative pathogens. Contemporary advancements incorporate enzymatic methods to resolve or synthesize chiral centers, exemplified by the use of oxidases or amidases to produce enantiopure β-hydroxy like (S)-β-hydroxyvaline, a key building block for monobactams such as tigemonam. These biocatalytic steps enhance yield and reduce waste compared to classical resolutions, facilitating large-scale production; such innovations build upon foundational patents from Squibb (now Bristol-Myers Squibb) that optimized overall process efficiency for pharmaceutical manufacturing. Natural precursors for these semi-synthetics derive from soil bacteria including and Flexibacter strains.

History

Discovery

In the 1970s, the widespread emergence of beta-lactamase-producing pathogens caused significant resistance to early penicillins and cephalosporins, driving pharmaceutical research toward novel beta-lactam structures resistant to enzymatic . A targeted screening program at the Squibb Institute for , initiated in the mid-1970s, sought bacterially produced beta-lactams with enhanced stability against gram-negative beta-lactamases and activity against aerobic . This effort culminated in the isolation of additional natural monobactams early in 1979, building on the prior discovery of the inaugural monobactam, nocardicin A, which had been isolated in 1976 through of the soil actinomycete Nocardia uniformis subsp. tsuyamanensis (ATCC 21806) by a Japanese research team, exhibiting moderate activity against such as Proteus and Pseudomonas species. Subsequent isolations included the monobactam nucleus SQ 81,761 from a related Nocardia uniformis strain in 1979 by the Squibb team, providing the core scaffold for further exploration. Additional natural producers emerged, such as Pseudomonas acidophila yielding sulfazecin in 1981, a sulfamic acid-containing monobactam with activity against gram-negative aerobes, and Chromobacterium violaceum producing related compounds such as SQ 26,180. Early structural elucidation of these monobactams, beginning with nocardicin A, relied on and () spectroscopy, revealing a single azetidinone ring devoid of fused structures typical of other beta-lactams. This monocyclic configuration was key to their stability and lack of immunological with penicillin-allergic patients, as confirmed by subsequent binding studies showing no interaction with penicillin-specific IgE antibodies.

Development

Following the isolation of natural monobactams from bacterial sources in the late , researchers at the Squibb Institute for Medical Research undertook extensive chemical modifications to address limitations in stability, solubility, and antibacterial potency of these compounds. These efforts focused on altering the side chains and moieties of the core monobactam ring, screening hundreds of synthetic analogs for improved pharmacokinetic properties and selective activity against . This optimization process led to the identification and selection of (SQ 26,776) in as the lead candidate, exhibiting enhanced resistance to beta-lactamases and superior activity compared to its natural precursors. Preclinical evaluation of involved systemic infection models in mice and rats, where it demonstrated high efficacy against a broad range of Gram-negative pathogens, including and , the latter being a key target due to its role in nosocomial infections. In these studies, achieved protective doses comparable to established beta-lactams like , with a wide attributed to its low toxicity and favorable distribution to infection sites such as the lungs and kidneys. Notably, showed synergistic effects when combined with aminoglycosides in Pseudomonas models, highlighting its potential for without cross-resistance concerns. Aztreonam advanced to human clinical trials in the early 1980s, beginning with phase I studies that established its safety and tolerability via intravenous administration, revealing minimal adverse effects even at high doses. Phase II and III trials, involving over 3,000 patients with serious Gram-negative infections such as , urinary tract infections, and septicemia, reported clinical cure or improvement rates exceeding 80% in evaluable cases, with bacteriological eradication in most instances. These results supported its efficacy as monotherapy or in combination, particularly against . The U.S. granted approval for (marketed as ) in December 1986, marking it as the first commercially available monobactam . Subsequent development efforts by other pharmaceutical companies yielded additional monobactams, though none achieved the global success of . Carumonam, synthesized by Takeda Pharmaceutical through modifications of sulfazecin, progressed through clinical trials in the mid-1980s and received approval in in 1987 for treating urinary tract and respiratory infections caused by susceptible ; however, its narrower spectrum and limited oral restricted international adoption. Similarly, tigemonam, an orally bioavailable analog developed by (ICI), underwent phase II and III trials in the late 1980s demonstrating good activity against but was discontinued in development around 1994 due to suboptimal efficacy against species and concerns over emerging resistance patterns.

Pharmacology

Mechanism of action

Monobactams exert their antibacterial effects by irreversibly binding to (PBPs), particularly PBP-3 in , where they acylate the active-site serine residue (e.g., Ser307), forming a stable acyl-enzyme complex. This binding inhibits the transpeptidase activity of PBP-3, which is essential for the final stage of synthesis during . As a result, transpeptidation is disrupted, preventing cross-linking of the layer in the bacterial and leading to weakened structural integrity, especially at the . The inhibition of PBP-3 by monobactams is bactericidal, primarily through a time-dependent mechanism that promotes autolytic cell in actively dividing . This causes morphological changes such as filamentation, where cells elongate without septation, ultimately resulting in due to osmotic instability. The time-dependent nature underscores their efficacy against growing populations of Gram-negative pathogens, with killing rates enhanced by prolonged exposure above the . A key feature of monobactams is their resistance to by many serine-based β-lactamases, such as TEM-1, owing to their monocyclic β-lactam and the N1-sulfonic substituent, which hinders effective recognition and cleavage by these enzymes. However, they remain susceptible to metallo-β-lactamases, which utilize zinc-dependent to break the β-lactam ring. This selective stability contributes to their utility against certain β-lactamase-producing Gram-negative strains but limits broader applications. Monobactams demonstrate no significant activity against due to their poor affinity for the PBPs in these organisms, arising from structural mismatches that prevent effective binding and inhibition. This specificity confines their action to Gram-negative aerobes, where PBP-3 homology facilitates potent interaction.

Spectrum of activity

Monobactams, exemplified by , exhibit selective activity against aerobic Gram-negative , particularly members of the family such as and species, as well as . For susceptible strains, minimum inhibitory concentrations (MICs) of typically range from 0.5 to 8 μg/mL against these pathogens, with breakpoints defining susceptibility at ≤4 μg/mL for and ≤8 μg/mL for P. aeruginosa. This class of antibiotics shows no activity against , such as staphylococci, or anaerobic organisms, limiting their utility to infections caused exclusively by susceptible Gram-negatives. Additionally, monobactams are ineffective against most atypical pathogens and demonstrate poor coverage against extended-spectrum β-lactamase (ESBL)-producing strains unless combined with a β-lactamase inhibitor. In terms of comparative efficacy, provides broader coverage than early-generation cephalosporins, which generally lack activity against this organism, but its overall spectrum is narrower than that of , which encompass Gram-positives, anaerobes, and a wider range of Gram-negatives. studies have demonstrated synergy between aztreonam and aminoglycosides against resistant strains of P. aeruginosa and , enhancing bactericidal effects in combination regimens.

Medical uses

Indications

Aztreonam, the prototypical monobactam antibiotic, is FDA-approved for the treatment of several infections caused by susceptible aerobic , including complicated urinary tract infections (such as ), lower respiratory tract infections (such as and ), and intra-abdominal infections (such as ). These indications encompass pathogens like , , , and species, with efficacy demonstrated in both adult and pediatric patients. In addition, the inhaled formulation of (Cayston) is specifically approved for improving respiratory symptoms in patients aged 7 years and older with P. aeruginosa infections, addressing chronic pulmonary exacerbations in this population. The Infectious Diseases Society of America (IDSA) 2024 Guidance on the Treatment of Antimicrobial-Resistant Gram-Negative Infections endorses as a key alternative for beta-lactam-allergic individuals experiencing Gram-negative infections, particularly in scenarios like and in cancer patients. For instance, in high-risk neutropenic fever, combined with is recommended for patients with severe penicillin to provide empiric coverage against Gram-negative while minimizing risks. Similarly, for antimicrobial-resistant Gram-negative in allergic patients, IDSA guidance suggests , often paired with beta-lactamase inhibitors such as ceftazidime-avibactam, to target extended-spectrum -producing or metallo-beta-lactamase producers when other options are limited. In 2025, the FDA approved EMBLAVEO ( and avibactam) for injection, in combination with , for the treatment of complicated intra-abdominal infections (cIAI) in adults aged 18 years and older with limited or no alternative therapy options, caused by susceptible Gram-negative microorganisms including Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, Enterobacter cloacae complex, Citrobacter freundii complex, and Serratia marcescens. This approval expands monobactam use against certain resistant pathogens. Patient selection for monobactams emphasizes individuals with documented IgE-mediated beta-lactam allergies, as exhibits negligible cross-reactivity with penicillins, cephalosporins, or (except ceftazidime due to side-chain similarity). It is favored in such cases for its safety profile in allergy histories, but not as a first-line agent for polymicrobial infections, where broader coverage for Gram-positive or anaerobic organisms is required. Due to its spectrum limitations to aerobic Gram-negatives, is often necessary in complex clinical settings like intra-abdominal or mixed infections.

Administration and dosage

Monobactams, primarily represented by , are administered via intravenous (IV) infusion or intramuscular () injection, as they exhibit no oral . The standard adult dosage for systemic s is 1-2 g every 8 hours IV or IM, with adjustments based on severity; for moderately severe cases, 1-2 g every 8-12 hours is typical, while severe or life-threatening s may require 2 g every 6-8 hours, not exceeding 8 g per day. Doses of 1 g or less may be given IM for moderately severe s where IV access is not feasible. Aztreonam is supplied as a lyophilized powder in single-dose vials (500 mg, 1 g, or 2 g) for reconstitution with a compatible , such as sterile water or 0.9% , prior to administration. For patients with experiencing lung infections, an inhaled formulation (Cayston) is available: 75 mg (one vial reconstituted with 1 mL ) administered three times daily via for a 28-day course, followed by a 28-day off period, in adults and pediatric patients aged 7 years and older. Dosage adjustments are necessary for renal impairment; in adults with creatinine clearance (CrCl) of 10-30 mL/min/1.73 m², administer an initial of 1-2 g, followed by half the usual dose at the standard interval, while for CrCl <10 mL/min/1.73 m², reduce maintenance doses to one-fourth of the initial dose every 6-12 hours, with supplemental dosing after hemodialysis for severe infections. Pediatric dosing for systemic infections ranges from 30 mg/kg every 6-8 hours (up to 120 mg/kg/day maximum), divided based on severity, with similar renal adjustments applied proportionally. Therapy duration is typically 7-14 days but should continue for at least 48 hours after clinical resolution or bacterial eradication, extending longer for persistent or complicated infections based on susceptibility testing and patient response.

Adverse effects

Common reactions

Monobactams, exemplified by , are generally well-tolerated with a low overall incidence of adverse effects in clinical use. In domestic clinical trials involving over 2,000 patients, systemic adverse events occurred in approximately 1-2% of cases, primarily mild and transient, leading to drug discontinuation in less than 1% of patients. Gastrointestinal disturbances represent one of the most frequently reported categories of side effects. Diarrhea affects 1-1.4% of treated patients, while nausea and/or vomiting occur in 1-1.3%, typically resolving without intervention and described as mild and self-limiting. Local reactions at the injection site are also common, particularly with intravenous administration. Phlebitis or thrombophlebitis is observed in about 1.9% of cases, and intramuscular injections may cause discomfort or swelling in around 2.4% of patients. These effects are usually minor and do not necessitate treatment cessation. Laboratory abnormalities are infrequent but noteworthy. Transient elevations in liver enzymes, such as AST (SGOT) and ALT (SGPT), occur in 10% to 38% of patients during high-dose intravenous therapy, generally asymptomatic and reversible upon discontinuation; elevations exceeding three times the upper limit of normal are reported in 2-3% of cases. Eosinophilia is reported in approximately 4% of cases across trials. Overall, these mild reactions contrast with the relative rarity of severe hypersensitivities.

Hypersensitivity and contraindications

Monobactams, particularly aztreonam, are associated with a low incidence of hypersensitivity reactions, including anaphylaxis and urticaria, each occurring in less than 1% of patients. These reactions can manifest in individuals with or without prior exposure to the drug and may require immediate discontinuation and supportive care, such as epinephrine administration. Severe cutaneous reactions, including Stevens-Johnson syndrome, are rare but have been reported, often in patients with complicating factors like sepsis or immunosuppression. Due to their monocyclic beta-lactam structure, monobactams exhibit minimal cross-reactivity with penicillins, with rates below 1% in patients with IgE-mediated penicillin allergies, making them a safe alternative in such cases. Both preclinical and clinical data confirm that aztreonam rarely interacts with penicillin-specific IgE antibodies. Aztreonam is contraindicated in patients with known hypersensitivity to the drug or any of its components. Caution is advised in individuals with a history of carbapenem allergy, as immunological and limited clinical evidence suggests a potential for cross-reactivity, though overall rates remain low at under 1%. Skin testing for monobactam hypersensitivity is not routinely recommended as a standard practice, unlike for penicillins. Instead, close monitoring for signs of allergic response, such as rash development, is essential, with prompt discontinuation if any occur.

Research

Emerging monobactams

Ongoing research into monobactams in the 2020s has focused on developing derivatives that overcome limitations in spectrum of activity and penetration into Gram-negative bacteria, particularly multidrug-resistant (MDR) strains. These efforts include structural modifications to enhance stability against β-lactamases and improve delivery mechanisms, aiming to restore efficacy in treating complicated infections such as those caused by and species. Siderophore-conjugated monobactams represent a key class of novel agents designed for enhanced penetration into Gram-negative pathogens by exploiting bacterial iron uptake systems. For instance, MB-1, a conjugate linking a monobactam core to a siderophore mimic, demonstrates broad-spectrum in vitro activity against MDR Gram-negative bacteria, including efflux pump-overexpressing strains, by facilitating active transport across outer membranes. This compound remains in preclinical stages as of 2025, with studies highlighting its potential against Pseudomonas aeruginosa and other non-fermenters, though challenges like competition with endogenous siderophores have been noted. Similarly, BAL30072, a siderophore monosulfactam incorporating iron-chelating groups, exhibited potent activity against MDR isolates of Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacteriaceae, including those producing metallo-β-lactamases, in preclinical and early clinical studies. However, development was discontinued after Phase I trials due to hepatotoxicity concerns. These modifications, including the addition of iron-chelating moieties, also aim to target intracellular pathogens by improving uptake in iron-limited environments. Combination therapies have emerged as a practical approach to extend monobactam utility against resistant pathogens. Aztreonam-avibactam (Emblaveo), approved by the European Commission in April 2024 for treating complicated intra-abdominal infections, hospital-acquired pneumonia, and ventilator-associated pneumonia caused by MDR Gram-negative bacteria, pairs aztreonam with the non-β-lactam β-lactamase inhibitor avibactam to protect against serine β-lactamases while leveraging aztreonam's inherent stability to metallo-β-lactamases. In February 2025, the U.S. FDA approved aztreonam-avibactam (Emblaveo) for complicated intra-abdominal infections in adults with limited treatment options, with commercial availability beginning in Q3 2025. This combination shows high susceptibility rates (>99%) against , including carbapenem-resistant strains, in European surveillance studies conducted through 2025. Recent advances in the 2020s have also explored non-β-lactam mimics that retain elements of the monobactam scaffold or mechanism to combat MDR infections. Lactivicin derivatives, which emulate the serine protease inhibitory action of monobactams without a β-lactam ring, have been modified with siderophore-like groups to boost potency against in ; for example, acetamido-substituted variants show improved activity and remain in preclinical evaluation for broader antimicrobial applications. Additionally, synthetic efforts have yielded new monobactam sulfonates and piperidine-modified analogs, with select compounds demonstrating superior efficacy against MDR compared to alone. Other candidates, such as LYS228 (which reached Phase II clinical development for urinary tract and intra-abdominal infections before out-licensure) and AIC499 (in Phase I trials), further illustrate this trend toward scaffold-retaining innovations for coverage.

Resistance challenges

Bacterial resistance to monobactams, such as aztreonam, primarily arises through several key mechanisms that impair drug entry, enhance expulsion, or enable enzymatic degradation. Efflux pumps, particularly the MexAB-OprM system in Pseudomonas aeruginosa, actively export monobactams from the bacterial periplasm, reducing intracellular drug concentrations and conferring multidrug resistance. Similarly, loss or downregulation of outer membrane porins like OmpF in Enterobacteriaceae limits the passive diffusion of hydrophilic monobactams across the outer membrane, often in combination with other resistance factors to elevate minimum inhibitory concentrations. Metallo-β-lactamases, exemplified by NDM-1, hydrolyze the β-lactam ring of monobactams, although less efficiently than other β-lactams, leading to resistance particularly when co-expressed with additional β-lactamases like AmpC or ESBLs. The prevalence of monobactam resistance is increasing, especially among Gram-negative pathogens in high-risk environments. In (ICU) settings, resistance rates to in P. aeruginosa isolates often exceed 20%, with surveillance data from 2024-2025 indicating rates up to 22-57% depending on regional and institutional factors, driven by selective pressure from use. This rise contributes significantly to the burden of multidrug-resistant (MDR) Gram-negative infections, complicating treatment of nosocomial pathogens. To mitigate these challenges, counterstrategies focus on restoring monobactam susceptibility through synergistic combinations. inhibitors like avibactam protect monobactams from by serine-based enzymes, enabling effective activity against NDM-1-producing strains when paired with , as evidenced by the 2025 FDA approval of aztreonam-avibactam for complicated intra-abdominal infections caused by MDR Gram-negatives. with enhances bacterial killing by disrupting outer membrane integrity, synergizing with monobactams to overcome efflux and permeability barriers in resistant P. aeruginosa, with in vitro and studies demonstrating improved against MDR isolates. Globally, monobactam resistance exacerbates the threat of MDR , particularly carbapenem-resistant (CRE), which the classifies as a critical priority due to high mortality rates and limited therapeutic options. While monobactams retain utility against certain CRE subsets lacking hydrolytic enzymes, the emergence of combined resistance mechanisms underscores their role in driving the crisis, necessitating enhanced stewardship and novel interventions.

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