Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Bacterial membrane vesicles (BMVs) represent a class of nanoscale lipid particles released by both Gram-positive and Gram-negative bacteria, serving as versatile mediators of intercellular communication and host-pathogen interactions. Their unique biogenesis pathways and functional properties have positioned them as promising targets for therapeutic and biotechnological applications. To comprehensively assess the research trends of this dynamic research field, we conducted a bibliometric analysis of 6,352 studies on BMVs published between 1 January 2014 and 19 November 2024 using VOSviewer, CiteSpace, and the R package "bibliometrix." Our analysis revealed that the Chinese Academy of Sciences led institutional contributions, while Frontiers in Microbiology emerged as the most active journal. Kim, Yoon-Keun was the most prolific author, reflecting his significant influence in the field. Key research hotspots were categorized into four frontiers: biogenesis mechanisms, pathogenesis and immune regulation, clinical applications, and methodological and engineering innovations.

Download full-text PDF

Source
http://dx.doi.org/10.1080/21645515.2025.2511355DOI Listing

Publication Analysis

Top Keywords

bacterial membrane
8
membrane vesicles
8
bibliometric analysis
8
translational horizons
4
horizons bacterial
4
vesicles hotspots
4
hotspots frontiers
4
frontiers basic
4
basic medicine
4
medicine clinical
4

Similar Publications

This study investigates a multifunctional hydrogel system integrating carboxymethyl cellulose (CMC) in a 3D-printed limonene (LIM) scaffold coated with poly(3,4-ethylenedioxythiophene): polystyrene sulfonate (PEDOT:PSS). The system allows to enhance wound healing, prevent infections, and monitor the healing progress. CMC is crosslinked with citric acid (CA) to form the hydrogel matrix (CMC-CA), while the 3D-printed limonene (LIM) scaffold is embedded within the hydrogel to provide mechanical support.

View Article and Find Full Text PDF

Pentameric ligand-gated ion channels control synaptic neurotransmission via an allosteric mechanism, whereby agonist binding induces global protein conformational changes that open an ion-conducting pore. For the proton-activated bacterial () ligand-gated ion channel (GLIC), high-resolution structures are available in multiple conformational states. We used a library of atomistic molecular dynamics (MD) simulations to study conformational changes and to perform dynamic network analysis to elucidate the communication pathways underlying the gating process.

View Article and Find Full Text PDF

Plasmalogens are a subclass of glycerophospholipids characterized by a vinyl-ether bond at the sn-1 position; they play several physiological roles including membrane stabilization, antioxidant activity, and signal transduction. While choline, ethanolamine, serine, and glycerol plasmalogens (PlsCho, PlsEtn, PlsSer, and PlsGro) are naturally abundant, inositol plasmalogens (PlsIns) are rare. In contrast to the limited occurrence of PlsIns, phosphatidylinositol is a biologically crucial lipid, and its enzymatic biosynthesis from phosphatidylcholine has been extensively studied.

View Article and Find Full Text PDF

Outer membrane vesicles (OMVs) are nanosized vesicles naturally secreted by Gram-negative bacteria and represent a promising platform for vaccine development. OMVs possess inherent immunostimulatory properties due to the presence of pathogen-associated molecular patterns (PAMPs), providing self-adjuvanting capabilities and the ability to elicit both innate and adaptive immune responses. This review outlines the advantages of OMVs over traditional vaccine strategies, including their safety, modularity, and the potential for genetic engineering to enable targeted antigen delivery.

View Article and Find Full Text PDF

Background: Synergy between antibiotic pairs is typically discovered using chequerboard assays that assume uniform, static drug exposure; however, such conditions rarely apply in vivo. Dynamic and heterogeneous tissue environments create spatial and temporal mismatches in drug exposure that can uncouple synergistic interactions, leading to unexpected treatment failure.

Objective: This study aims to develop a physiologically relevant in vitro model that integrates infection-site microenvironments and drug-specific pharmacokinetics.

View Article and Find Full Text PDF