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
. 2020 Jun 21;8(6):935.
doi: 10.3390/microorganisms8060935.

Antibiotic Resistance Profiles, Molecular Mechanisms and Innovative Treatment Strategies of Acinetobacter baumannii

Affiliations
Review

Antibiotic Resistance Profiles, Molecular Mechanisms and Innovative Treatment Strategies of Acinetobacter baumannii

Corneliu Ovidiu Vrancianu et al. Microorganisms. .

Abstract

Antibiotic resistance is one of the biggest challenges for the clinical sector and industry, environment and societal development. One of the most important pathogens responsible for severe nosocomial infections is Acinetobacter baumannii, a Gram-negative bacterium from the Moraxellaceae family, due to its various resistance mechanisms, such as the β-lactamases production, efflux pumps, decreased membrane permeability and altered target site of the antibiotic. The enormous adaptive capacity of A. baumannii and the acquisition and transfer of antibiotic resistance determinants contribute to the ineffectiveness of most current therapeutic strategies, including last-line or combined antibiotic therapy. In this review, we will present an update of the antibiotic resistance profiles and underlying mechanisms in A. baumannii and the current progress in developing innovative strategies for combating multidrug-resistant A. baumannii (MDRAB) infections.

Keywords: Acinetobacter baumannii; CRISPR; antimicrobial peptide; antimicrobial resistance; bacteriophage; β-lactamases.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Schematic representation of clustered regularly interspaced short palindromic repeat (CRISPR)-based targeting of mobile genetic elements (MGEs). This system contains the cas9 nuclease, sgRNA transcript and other structural elements. In the first stage, sgRNA forms a complex with Cas 9 nuclease. The sgRNA transcript guide cas9 nuclease to introduce double-stranded breaks at the ends of the target DNA, leading to cleavage. Direct target recognition is achieved by recognizing protospacer adjacent motifs (PAM), short DNA sequences that are not found in CRISPR loci, so there is no risk of self-degradation. This system can be used to edit the genome of several antibiotic-resistant bacterial strains, leading to the removal of resistance determinants. Figure created with https://biorender.com/.

References

    1. O’Neill J. Tackling Drug-Resistance Infections Globally: Final Report and Recommendations. The Review on Antimicrobial Resistance. Government of the United Kingdom; London, UK: 2016. pp. 1–84.
    1. Monserrat-Martinez A., Gambin Y., Sierecki E. Thinking Outside the Bug: Molecular Targets and Strategies to Overcome Antibiotic Resistance. Int. J. Mol. Sci. 2019;20:1255. doi: 10.3390/ijms20061255. - DOI - PMC - PubMed
    1. Holmes A.H., Moore L.S.P., Sundsfjord A., Steinbakk M., Regmi S., Karkey A., Guerin P.J., Piddock L.J.V. Understanding the Mechanisms and Drivers of Antimicrobial Resistance. Lancet. 2016;387:176–187. doi: 10.1016/S0140-6736(15)00473-0. - DOI - PubMed
    1. Eze E.C., Chenia H.Y., El Zowalaty M.E. Acinetobacter Baumannii Biofilms: Effects of Physicochemical Factors, Virulence, Antibiotic Resistance Determinants, Gene Regulation, and Future Antimicrobial Treatments. Infect. Drug Resist. 2018;11:2277–2299. doi: 10.2147/IDR.S169894. - DOI - PMC - PubMed
    1. Nemec A., Krizova L., Maixnerova M., van der Reijden T.J.K., Deschaght P., Passet V., Vaneechoutte M., Brisse S., Dijkshoorn L. Genotypic and Phenotypic Characterization of the Acinetobacter Calcoaceticus-Acinetobacter Baumannii Complex with the Proposal of Acinetobacter Pittii Sp. Nov. (Formerly Acinetobacter Genomic Species 3) and Acinetobacter Nosocomialis Sp. Nov. (formerly Acinetobacter genomic species 13TU) Res. Microbiol. 2011;162:393–404. doi: 10.1016/j.resmic.2011.02.006. - DOI - PubMed