ReviewArchives of microbiology2025
Acinetobacter baumannii-rare virulence factors and pathogenesis: the impact of biofilm associated protein (Bap), outer membrane vesicles, and iron acquisition system.
Review in Archives of microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Acinetobacter baumannii is an opportunistic pathogen that poses a significant threat to the global healthcare system. It is a member of Extensively Drug-Resistant pathogens and one of the critical priority pathogens listed by the World Health Organisation. Bacteria develop resistance to various types of antibiotics through genetic adaptation. While numerous studies have concentrated on common virulence factors, we here focus on uncommon and underexplored virulence factors, such as biofilm-associated proteins, outer membrane vesicles, and the iron acquisition system of A. baumannii. Biofilm-associated proteins, including the chaperone-usher system, play a crucial role in the formation and stability of biofilms, providing a protective niche that enhances resistance to antibiotics and environmental stresses. Outer membrane vesicles bound to AbOmpA play a predominant role in delivering virulence factors into host cells, facilitating inter-bacterial communication through quorum sensing and modulating host-pathogen interactions. Iron acquisition systems, involving siderophores, TonB, and AbHemO, are used to acquire iron from the host cell or from the environment for bacterial growth and metabolism in an iron-limited environment. By integrating insights into the structural, regulatory, and functional aspects of these uncommon virulence factors, this review outlines their synergistic contribution to A. baumannii pathogenicity. Additionally, it examines emerging anti-virulence and resistance-modifying strategies that target these factors. Such understanding provides a foundation for developing targeted therapeutic interventions against multidrug-resistant A. baumannii infections.
Indexed as
Identifiers
41379337What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.