Acinetobacter baumannii: Pathogenesis, virulence factors, novel therapeutic options and mechanisms of resistance to antimicrobial agents with emphasis on tigecycline
- PMID: 36200470
- DOI: 10.1111/jcpt.13787
Acinetobacter baumannii: Pathogenesis, virulence factors, novel therapeutic options and mechanisms of resistance to antimicrobial agents with emphasis on tigecycline
Abstract
What is known and objective: Acinetobacter baumannii is one of the most important nosocomial pathogens with the ability to cause infections such as meningitis, pneumonia, urinary tract, septicaemia and wound infections. A wide range of virulence factors are responsible for pathogenesis and high mortality of A. baumannii including outer membrane proteins, lipopolysaccharide, capsule, phospholipase, nutrient- acquisition systems, efflux pumps, protein secretion systems, quarom sensing and biofilm production. These virulence factors contribute in pathogen survival in stressful conditions and antimicrobial resistance.
Comment: According to the World Health Organization (WHO), A. baumannii is one of the most resistant pathogens of ESKAPE group (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, A. baumannii, Pseudomonas aeruginosa and Enterobacter spp.). In recent years, resistance to a wide range of antibiotics in A. baumannii has significantly increased and the high emergence of extensively drug resistant (XDR) isolates is challenging. Among therapeutic antibiotics, resistance to tigecycline as a last resort antibiotic has become a global concern. Several mechanisms are involved in tigecycline resistance, the most important of which is RND (Resistance-Nodulation-Division) family efflux pumps overexpression. The development of new therapeutic strategies to confront A. baumannii infections has been very promising in recent years.
What is new and conclusion: In the present review we highlight microbiological and virulence traits in A. baumannii and peruse the tigecycline resistance mechanisms and novel therapeutic options. Among the novel therapeutic strategies we focus on combination therapy, drug repurposing, novel antibiotics, bacteriophage therapy, antimicrobial peptides (AMPs), human monoclonal antibodies (Hu-mAbs), nanoparticles and gene editing.
Keywords: Acinetobacter baumannii; combination therapy; drug repurposing; mechanism of antibiotic resistance; pathogenesis; phage therapy; tigecycline; treatment options; virulence factors.
© 2022 John Wiley & Sons Ltd.
Similar articles
-
Genomic and Phenotypic Evolution of Tigecycline-Resistant Acinetobacter baumannii in Critically Ill Patients.Microbiol Spectr. 2022 Feb 23;10(1):e0159321. doi: 10.1128/spectrum.01593-21. Epub 2022 Jan 19. Microbiol Spectr. 2022. PMID: 35044218 Free PMC article.
-
Tigecycline Heteroresistance and Resistance Mechanism in Clinical Isolates of Acinetobacter baumannii.Microbiol Spectr. 2021 Oct 31;9(2):e0101021. doi: 10.1128/Spectrum.01010-21. Epub 2021 Sep 15. Microbiol Spectr. 2021. PMID: 34523993 Free PMC article.
-
Synergistic pathogenesis: exploring biofilms, efflux pumps and secretion systems in Acinetobacter baumannii and Staphylococcus aureus.Arch Microbiol. 2025 May 2;207(6):134. doi: 10.1007/s00203-025-04336-w. Arch Microbiol. 2025. PMID: 40314822 Review.
-
The role of quorum sensing, biofilm formation, and iron acquisition as key virulence mechanisms in Acinetobacter baumannii and the corresponding anti-virulence strategies.Microbiol Res. 2022 Jul;260:127032. doi: 10.1016/j.micres.2022.127032. Epub 2022 Apr 12. Microbiol Res. 2022. PMID: 35483311 Review.
-
Resistance mechanisms of tigecycline in Acinetobacter baumannii.Front Cell Infect Microbiol. 2023 May 9;13:1141490. doi: 10.3389/fcimb.2023.1141490. eCollection 2023. Front Cell Infect Microbiol. 2023. PMID: 37228666 Free PMC article. Review.
Cited by
-
A fresh pH-responsive imipenem-loaded nanocarrier against Acinetobacter baumannii with a synergetic effect.Front Bioeng Biotechnol. 2023 Apr 11;11:1166790. doi: 10.3389/fbioe.2023.1166790. eCollection 2023. Front Bioeng Biotechnol. 2023. PMID: 37113664 Free PMC article.
-
Green-Synthesized Zinc Oxide Nanoparticles for Acinetobacter baumannii Control: A Review of Plant-Based Approaches.Cureus. 2025 May 5;17(5):e83506. doi: 10.7759/cureus.83506. eCollection 2025 May. Cureus. 2025. PMID: 40470438 Free PMC article. Review.
-
Epidemiology of Acinetobacter baumannii: analysis of hazard factors associated with positivity cases in Guizhou province, China from 2015 to 2023.Front Public Health. 2025 Jul 3;13:1592783. doi: 10.3389/fpubh.2025.1592783. eCollection 2025. Front Public Health. 2025. PMID: 40678652 Free PMC article.
-
Antimicrobial peptide 2K4L disrupts the membrane of multidrug-resistant Acinetobacter baumannii and protects mice against sepsis.Front Microbiol. 2023 Oct 24;14:1258469. doi: 10.3389/fmicb.2023.1258469. eCollection 2023. Front Microbiol. 2023. PMID: 37942076 Free PMC article.
-
Acinetobacter Baumannii Phages: Past, Present and Future.Viruses. 2023 Mar 3;15(3):673. doi: 10.3390/v15030673. Viruses. 2023. PMID: 36992382 Free PMC article. Review.
References
REFERENCES
-
- Howard A, O'Donoghue M, Feeney A, Sleator RD. Acinetobacter baumannii: an emerging opportunistic pathogen. Virulence. 2012;3(3):243-250.
-
- Peleg AY, Seifert H, Paterson DL. Acinetobacter baumannii: emergence of a successful pathogen. Clin Microbiol Rev. 2008;21(3):538-582.
-
- Vijayakumar S, Biswas I, Veeraraghavan B. Accurate identification of clinically important Acinetobacter spp.: an update. Future Science OA. 2019;5(7):FSO395.
-
- Villalón P, Ortega M, Sáez-Nieto JA, et al. Dynamics of a sporadic nosocomial Acinetobacter calcoaceticus-Acinetobacter baumannii complex population. Front Microbiol. 2019;10:593.
-
- Vincent J-L, Rello J, Marshall J, et al. International study of the prevalence and outcomes of infection in intensive care units. JAMA. 2009;302(21):2323-2329.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous