Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Dec 10;11(12):1793.
doi: 10.3390/antibiotics11121793.

Acinetobacter baumannii Resistance to Sulbactam/Durlobactam: A Systematic Review

Affiliations
Review

Acinetobacter baumannii Resistance to Sulbactam/Durlobactam: A Systematic Review

Luigi Principe et al. Antibiotics (Basel). .

Abstract

Infections caused by carbapenem-resistant Acinetobacter baumannii (CRAB) have limited therapeutic options. Sulbactam-durlobactam is a combination of two βlactamase inhibitors with activity against CRAB under phase 3 clinical investigation. We performed a systematic review on in vitro studies reporting A. baumannii resistances against sulbactam/durlobactam. We considered "resistant" species to be those with MIC ≥ 8 mg/L. Ten studies were included in the review (9754 tested isolates). Overall, 2.3% of A. baumannii were resistant to sulbactam/durlobactam, and this percentage rose to 3.4% among CRAB subgroups and to 3.7% among colistin-resistant strains. Resistance was 100% among metallo β-lactamase-producing strains. Overall, in 12.5% of cases, sulbactam/durlobactam resistance was associated with the production of NDM-1, in 31.7% of cases with the substitutions in the PBP3 determinants, and in the remaining cases the resistance mechanism was unknown. In conclusion, A. baumannii resistance towards sulbactam/durlobactam is limited, except for MBL-producing strains.

Keywords: Acinetobacter; efficacy; resistance; resistances; sulbactam-durlobactam; sulbactam/durlobactam; susceptibility.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Search strategy.

References

    1. Kumar S., Anwer R., Azzi A. Virulence Potential and Treatment Options of Multidrug-Resistant (MDR) Microorganisms. 2021;9:2104. doi: 10.3390/microorganisms9102104. - DOI - PMC - PubMed
    1. Vrancianu C.O., Gheorghe I., Czobor I.B., Chifiriuc M.C. Antibiotic Resistance Profiles, Molecular Mechanisms and Innovative Treatment Strategies of Acinetobacter baumannii. Microorganisms. 2020;8:935. doi: 10.3390/microorganisms8060935. - DOI - PMC - PubMed
    1. Hamidian M., Nigro S.J. Emergence, Molecular Mechanisms and Global Spread of Carbapenem-Resistant. Microb. Genom. 2019;5:e000306. doi: 10.1099/mgen.0.000306. - DOI - PMC - PubMed
    1. Principe L., Lupia T., Andriani L., Campanile F., Carcione D., Corcione S., De Rosa F.G., Luzzati R., Stroffolini G., Steyde M., et al. Microbiological, Clinical, and PK/PD Features of the New Anti-Gram-Negative Antibiotics: β-Lactam/β-Lactamase Inhibitors in Combination and Cefiderocol-An All-Inclusive Guide for Clinicians. Pharmaceuticals. 2022;15:463. doi: 10.3390/ph15040463. - DOI - PMC - PubMed
    1. Bassetti M., Echols R., Matsunaga Y., Ariyasu M., Doi Y., Ferrer R., Lodise T.P., Naas T., Niki Y., Paterson D.L., et al. Efficacy and Safety of Cefiderocol or Best Available Therapy for the Treatment of Serious Infections Caused by Carbapenem-Resistant Gram-Negative Bacteria (CREDIBLE-CR): A Randomised, Open-Label, Multicentre, Pathogen-Focused, Descriptive, Phase 3 Trial. Lancet Infect. Dis. 2021;21:226–240. doi: 10.1016/S1473-3099(20)30796-9. - DOI - PubMed

LinkOut - more resources