A plasmid-associated immunoglobulin-binding protein in Acinetobacter baumannii

Background A cinetobacter baumannii is a critical global health threat due to multidrug resistance and high mortality. Although antimicrobial resistance mechanisms are well characterised, the virulence determinants that drive severe infections remain poorly understood. Methods We screened 89 carbapenem-resistant clinical isolates of A. baumannii for virulence in animal infection models and combined comparative genomics with functional assays to identify virulence factors. An im munoglobulin- b inding protein from A . baumannii (ImbA) encoded on the type D plasmid was selected and characterised. Protein–immunoglobulin interactions were analysed by pull-down and biolayer interferometry. Additional ImbA inhibition of IgG–Fcγ receptor binding by flow cytometry were tested. Protective efficacy was evaluated in mice using vaccination or anti-ImbA antibodies. Findings A type D plasmid was consistently linked to high virulence in clinical isolates. The deletion of plasmid-encoded ImbA attenuated virulence. ImbA bound murine IgA and IgG with high affinity. The binding to the Fc region of IgG disrupted IgG–Fcγ receptor interactions. Vaccination with recombinant ImbA improved survival and reduced bacterial dissemination in female mice with anti-ImbA antibodies partially protecting against lethal infection. Bacterial burdens in the blood were reduced in treated groups. Interpretation Our study demonstrates ImbA as an unrecognised plasmid-encoded virulence factor in A. baumannii . By intercepting host immunoglobulins, ImbA drives immune evasion and hypervirulence. Blocking ImbA by vaccination and antibody therapy restored host defence and improved outcomes in female mice, highlighting ImbA as a non-antibiotic therapeutic target with potential against multidrug-resistant A. baumannii . Funding Bio&Medical Technology Development Program of the National Research Foundation (NRF), funded by the Korean government (MSIT) (No. RS-2023-00219213); Korea Research Institute of Bioscience and Biotechnology (KRIBB) Research Initiative Program.

Authors

Institutions

Publication Details

Journal
EBioMedicine
Published
2026-08-24
DOI
https://doi.org/10.1016/j.ebiom.2026.106445
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A plasmid-associated immunoglobulin-binding protein in Acinetobacter baumannii

Haeyoung Jeong, Choong‐Min Ryu, Min-Seon Park, Soohyun Lee et al.
EBioMedicine
Antibiotic Resistance in Bacteria
article

A plasmid-associated immunoglobulin-binding protein in Acinetobacter baumannii

Haeyoung Jeong, Choong‐Min Ryu, Min-Seon Park, Soohyun Lee, Jae‐Yoon Kim, Solip Lee, Nam-Kyung Lee, Dajeong Kim, Jihyun Yang, Hwi Won Seo, Kyungjin Lee, Hyuna Lim, Eui-Jeon Woo, Cheong Kim, Min Young Jeon
article en

Abstract

Background A cinetobacter baumannii is a critical global health threat due to multidrug resistance and high mortality. Although antimicrobial resistance mechanisms are well characterised, the virulence determinants that drive severe infections remain poorly understood. Methods We screened 89 carbapenem-resistant clinical isolates of A. baumannii for virulence in animal infection models and combined comparative genomics with functional assays to identify virulence factors. An im munoglobulin- b inding protein from A . baumannii (ImbA) encoded on the type D plasmid was selected and characterised. Protein–immunoglobulin interactions were analysed by pull-down and biolayer interferometry. Additional ImbA inhibition of IgG–Fcγ receptor binding by flow cytometry were tested. Protective efficacy was evaluated in mice using vaccination or anti-ImbA antibodies. Findings A type D plasmid was consistently linked to high virulence in clinical isolates. The deletion of plasmid-encoded ImbA attenuated virulence. ImbA bound murine IgA and IgG with high affinity. The binding to the Fc region of IgG disrupted IgG–Fcγ receptor interactions. Vaccination with recombinant ImbA improved survival and reduced bacterial dissemination in female mice with anti-ImbA antibodies partially protecting against lethal infection. Bacterial burdens in the blood were reduced in treated groups. Interpretation Our study demonstrates ImbA as an unrecognised plasmid-encoded virulence factor in A. baumannii . By intercepting host immunoglobulins, ImbA drives immune evasion and hypervirulence. Blocking ImbA by vaccination and antibody therapy restored host defence and improved outcomes in female mice, highlighting ImbA as a non-antibiotic therapeutic target with potential against multidrug-resistant A. baumannii . Funding Bio&Medical Technology Development Program of the National Research Foundation (NRF), funded by the Korean government (MSIT) (No. RS-2023-00219213); Korea Research Institute of Bioscience and Biotechnology (KRIBB) Research Initiative Program.

EBioMedicineVol. 131
Genome Research Foundation (KR), Korea Research Institute of Bioscience and Biotechnology (KR), Korea University of Science and Technology (KR)
Openalex Percentile: Top 18%
Antibiotic Resistance in Bacteria
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.