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Updated: Dec 20, 2025

Author Spotlight: Advancing Antibiotic Resistance Research Using an Efflux-Deficient Bacterial Strain and a Single-Copy Gene Expression System
Published on: January 5, 2024
Pan-transcriptomic analysis identified common differentially expressed genes of Acinetobacter baumannii in response
Mengyao Li1, Su Mon Aye, Maizbha Uddin Ahmed
1Biomedicine Discovery Institute, Infection & Immunity Program and Department of Microbiology, Monash University, 19 Innovation Walk, Melbourne 3800, Australia. yan.zhu@monash.edu jian.li@monash.edu.
Abstract:
Multidrug-resistant Acinetobacter baumannii is a top-priority Gram-negative pathogen and polymyxins are a last-line therapeutic option. Previous systems pharmacological studies examining polymyxin killing and resistance usually focused on individual strains, and the derived knowledge could be limited by strain-specific genomic context. In this study, we examined the gene expression of five A. baumannii strains (34654, 1207552, 1428368, 1457504 and ATCC 19606) to determine the common differentially expressed genes in response to polymyxin treatments. A pan-genome containing 6061 genes was identified for 89 A. baumannii genomes from RefSeq database which included the five strains examined in this study; 2822 of the 6061 genes constituted the core genome. After 2 mg L-1 or 0.75 × MIC polymyxin treatments for 15 min, 41 genes were commonly up-regulated, including those involved in membrane biogenesis and homeostasis, lipoprotein and phospholipid trafficking, efflux pump and poly-N-acetylglucosamine biosynthesis; six genes were commonly down-regulated, three of which were related to fatty acid biosynthesis. Additionally, comparison of the gene expression at 15 and 60 min in ATCC 19606 revealed that polymyxin treatment resulted in a rapid change in amino acid metabolism at 15 min and perturbations on envelope biogenesis at both time points. This is the first pan-transcriptomic study for polymyxin-treated A. baumannii and our results identified that the remodelled outer membrane, up-regulated efflux pumps and down-regulated fatty acid biosynthesis might be essential for early responses to polymyxins in A. baumannii. Our findings provide important mechanistic insights into bacterial responses to polymyxin killing and may facilitate the optimisation of polymyxin therapy against this problematic 'superbug'.
Insights
Multidrug-resistant Acinetobacter baumannii responds to polymyxins by up-regulating genes for membrane repair and efflux pumps, while down-regulating fatty acid synthesis. This pan-transcriptomic study reveals key mechanisms for combating this superbug.
Area of Science:
- Microbiology
- Genomics
- Pharmacology
Background:
- Multidrug-resistant Acinetobacter baumannii is a critical Gram-negative pathogen.
- Polymyxins are last-resort antibiotics, but resistance is increasing.
- Previous studies on polymyxin resistance were limited by strain-specific genomic data.
Purpose of the Study:
- To identify common gene expression changes in A. baumannii in response to polymyxin treatment across multiple strains.
- To understand the pan-genome and core genome of A. baumannii relevant to polymyxin resistance.
- To investigate the temporal dynamics of gene expression changes following polymyxin exposure.
Main Methods:
- Comparative transcriptomics of five A. baumannii strains treated with polymyxins.
- Pan-genome and core genome analysis of 89 A. baumannii genomes.
- Analysis of gene expression at 15 and 60 minutes post-treatment.
Main Results:
- 41 genes commonly up-regulated, including those involved in membrane biogenesis, homeostasis, and efflux pump activity.
- Six genes commonly down-regulated, notably three related to fatty acid biosynthesis.
- Polymyxin treatment rapidly altered amino acid metabolism and envelope biogenesis.
Conclusions:
- The study is the first pan-transcriptomic analysis of polymyxin-treated A. baumannii.
- Remodeled outer membrane, increased efflux pump activity, and reduced fatty acid synthesis are crucial early responses.
- Findings offer mechanistic insights to optimize polymyxin therapy against A. baumannii infections.

