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.

Molecular Omics
|May 30, 2020
PubMed

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.

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