# Activity of ceftolozane/tazobactam and imipenem/relebactam against clinical isolates of Enterobacterales and Pseudomonas aeruginosa collected in Greece and Italy—SMART 2017–2021

**Authors:** James A. Karlowsky, Sibylle H. Lob, Stephen P. Hawser, Nimmi Kothari, Fakhar Siddiqui, Irina Alekseeva, C. Andrew DeRyke, Katherine Young, Mary R. Motyl, Daniel F. Sahm

PMC · DOI: 10.1007/s10096-024-04756-4 · 2024-05-22

## TL;DR

This study assesses the effectiveness of two antibiotic combinations against bacterial infections in Greece and Italy, finding they work well against many strains.

## Contribution

The study provides new data on the efficacy of ceftolozane/tazobactam and imipenem/relebactam against clinical isolates in southern Europe.

## Key findings

- Ceftolozane/tazobactam inhibited 85–87% of Enterobacterales and 94–96% of ESBL-positive isolates.
- Imipenem/relebactam inhibited 95–98% of non-CRE NME isolates and 98–99% of KPC-positive isolates.
- Both antibiotics inhibited 84% of P. aeruginosa isolates from Greece and 91–92% from Italy.

## Abstract

The current study evaluated the in vitro activities of ceftolozane/tazobactam (C/T), imipenem/relebactam (IMI/REL), and comparators against recent (2017–2021) clinical isolates of gram-negative bacilli from two countries in southern Europe.

Nine clinical laboratories (two in Greece; seven in Italy) each collected up to 250 consecutive gram-negative isolates per year from lower respiratory tract, intraabdominal, urinary tract, and bloodstream infection samples. MICs were determined by the CLSI broth microdilution method and interpreted using 2022 EUCAST breakpoints. β-lactamase genes were identified in select β-lactam-nonsusceptible isolate subsets.

C/T inhibited the growth of 85–87% of Enterobacterales and 94–96% of ESBL-positive non-CRE NME (non-Morganellaceae Enterobacterales) isolates from both countries. IMI/REL inhibited 95–98% of NME, 100% of ESBL-positive non-CRE NME, and 98–99% of KPC-positive NME isolates from both countries. Country-specific differences in percent susceptible values for C/T, IMI/REL, meropenem, piperacillin/tazobactam, levofloxacin, and amikacin were more pronounced for Pseudomonas aeruginosa than Enterobacterales. C/T and IMI/REL both inhibited 84% of P. aeruginosa isolates from Greece and 91–92% of isolates from Italy. MBL rates were estimated as 4% of Enterobacterales and 10% of P. aeruginosa isolates from Greece compared to 1% of Enterobacterales and 3% of P. aeruginosa isolates from Italy. KPC rates among Enterobacterales isolates were similar in both countries (7–8%). OXA-48-like enzymes were only identified in Enterobacterales isolates from Italy (1%) while GES carbapenemase genes were only identified in P. aeruginosa isolates from Italy (2%).

We conclude that C/T and IMI/REL may provide viable treatment options for many patients from Greece and Italy.

## Linked entities

- **Chemicals:** ceftolozane/tazobactam (PubChem CID 86291594), meropenem (PubChem CID 441130), piperacillin/tazobactam (PubChem CID 461573), levofloxacin (PubChem CID 149096), amikacin (PubChem CID 37768)
- **Diseases:** urinary tract infection (MONDO:0005247)
- **Species:** Enterobacterales (taxon 91347), Pseudomonas aeruginosa (taxon 287)

## Full-text entities

- **Genes:** REM1 (RRAD and GEM like GTPase 1) [NCBI Gene 28954] {aka GD:REM, GES}
- **Diseases:** NME (MESH:C580335), bloodstream infection (MESH:D018805), gram-negative (MESH:D016905)
- **Species:** Enterobacterales (order) [taxon 91347], Homo sapiens (human, species) [taxon 9606], Pseudomonas aeruginosa (species) [taxon 287]

---
Source: https://tomesphere.com/paper/PMC11271313