P-1333. Activity of Zosurabalpin and Comparator Antimicrobial Agents Tested Against Acinetobacter baumannii-calcoaceticus complex (ABC) Isolates Collected Worldwide in 2024

TL;DR

Zosurabalpin is a new antibiotic that effectively targets drug-resistant Acinetobacter bacteria, including those resistant to other newer drugs.

Contribution

Zosurabalpin shows potent activity against carbapenem-resistant and multidrug-resistant Acinetobacter isolates, including those resistant to cefiderocol and sulbactam-durlobactam.

Findings

Zosurabalpin inhibited 99.7% of Acinetobacter isolates at ≤1 mg/L.

Zosurabalpin was effective against isolates resistant to cefiderocol and sulbactam-durlobactam.

Zosurabalpin's activity was consistent against both carbapenem-resistant and multidrug-resistant strains.

Abstract

Zosurabalpin (ZAB, RG6006) is a novel tethered macrocyclic peptide antibiotic that targets intracellular transport of lipopolysaccharide inhibiting the LptB2FGC complex. This agent has demonstrated in vitro activity against Acinetobacter baumannii-calcoaceticus complex (ABC) clinical isolates, including carbapenem-resistant (CRABC) and multidrug-resistant (MDR) strains. We evaluated the activity of ZAB against 1,575 ABC bacterial isolates collected during 2024 in a global surveillance program.Activity of zosurabalpin and comparator agents against ABC isolates

Activity of zosurabalpin and comparator agents against ABC isolates

Isolates were collected in 109 hospitals in Asia-Pacific (9 hospitals; n=166), Europe (39; n=747), Latin America (7; n=100) and the USA (54; n=562). Isolates originated from patients hospitalized with pneumonia (n=586), skin and skin structure infections (n=312), bloodstream infections(n=208), urinary tract infections (n=30), and other infections (n=293). Susceptibility testing was performed by the CLSI reference broth microdilution method. ZAB was tested in CAMHB supplemented with 20% heat-inactivated horse serum. CLSI and FDA interpretative criteria were applied. CRABC were resistant (R) to imipenem and/or meropenem and MDR were R to ≥ 3 antimicrobial classes applying CLSI breakpoints.

ZAB (MIC50/90, 0.12/0.5 mg/L) inhibited all ABC isolates at ≤ 2 mg/L and 99.7% at ≤ 1 mg/L. Among comparators, cefiderocol (FDC) and sulbactam-durlobactam (SUD) were the most active agents inhibiting 92.9% and 95.2% of the isolates, respectively (Table). The activity of ZAB was similar against CRABC (n=724 [46.0% overall]; MIC50/90, 0.25/0.5 mg/L) and MDR (n=761 [48.3%]; MIC50/90, 0.25/0.5 mg/L) isolates, inhibiting 99.7% at ≤1 mg/L and 100% at ≤ 2 mg/L. FDC and SUD inhibited 86.3% and 89.6% of the CRABC isolates and 86.6% and 90.1% of the MDR isolates, respectively. The activity of other comparators was markedly reduced against CRABC and MDR isolates. FDC-R (n=74), SUD-R (n=62) and 24 isolates resistant to both agents were all inhibited by ZAB at ≤ 1 mg/L.

ABC isolates are often CRABC and MDR and therapeutic options against these isolates remain limited. Zosurabalpin was active against CRABC and MDR ABC isolates and isolates resistant to novel agents including FDC and SUD. Further development of this agent is warranted.

Mariana Castanheira, PhD, Melinta Therapeutics: Advisor/Consultant|Melinta Therapeutics: Grant/Research Support Kelley A. Fedler, BS, Melinta Therapeutics: Grant/Research Support

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