Multi-omics approach to study global changes in a triclosan-resistant mutant strain of Acinetobacter baumannii ATCC 17978

Int J Antimicrob Agents. 2017 Jan;49(1):74-80. doi: 10.1016/j.ijantimicag.2016.10.014. Epub 2016 Dec 2.

Abstract

Acinetobacter baumannii AB042, a triclosan-resistant mutant strain, was examined for modulated gene expression using whole-genome sequencing, transcriptomics and proteomics in order to understand the mechanism of triclosan resistance as well as its impact on A. baumannii. Data revealed modulated expression of the fatty acid metabolism pathway, co-factors known to play a role in the synthesis of fatty acids, as well as several transcriptional regulators. The membrane composition of the mutant revealed a decrease in C18 with a corresponding increase in C16 fatty acids compared with the parent strain A. baumannii ATCC 17978. These data indicate that A. baumannii responds to triclosan by altering the expression of genes involved in fatty acid metabolism, antibiotic resistance and amino acid metabolism.

Keywords: Genomics; Global gene response; Proteomics; RNA-Seq.

MeSH terms

  • Acinetobacter baumannii / drug effects*
  • Anti-Infective Agents, Local / pharmacology*
  • Drug Resistance, Bacterial*
  • Gene Expression Profiling*
  • Genome, Bacterial*
  • Lipid Metabolism
  • Metabolic Networks and Pathways / genetics
  • Mutation
  • Proteome / analysis*
  • Sequence Analysis, DNA
  • Triclosan / pharmacology*

Substances

  • Anti-Infective Agents, Local
  • Proteome
  • Triclosan