A1S_2811, a CheA/Y-like hybrid two-component regulator from Acinetobacter baumannii ATCC17978, is involved in surface motility and biofilm formation in this bacterium

Microbiologyopen. 2017 Oct;6(5):e00510. doi: 10.1002/mbo3.510. Epub 2017 Jul 17.

Abstract

Two-component systems in Acinetobacter baumannii are associated with its virulence, drug resistance, motility, biofilm formation, and other characteristics. In this study, we used RecAb , a genetic engineering method, to investigate the function of A1S_2811 in A. baumannii strain ATCC17978. A1S_2811, a hypothetical hybrid sensor histidine kinase/response regulator, has four histidine-containing phosphotransfer domains, a CheA-like regulatory domain, and a CheY-like receiver domain at its C terminus. Compared with the ATCC17978 strain, both surface motility and biofilm formation at the gas-liquid interface decreased significantly in the A1S_2811 knock-out strain. The number of pilus-like structures and the amount of extrapolymeric substances on the cell surface also decreased in the A1S_2811 null strain. Transcription of abaI, which encodes an N-acylhomoserine lactone synthase in A. baumannii , decreased significantly in the A1S_2811 null strain, and supplementation with synthetic N-(3-oxodecanoyl) homoserine-l-lactone rescued the surface motility and biofilm formation phenotype in the null mutant. We speculate that A1S_2811 regulates surface motility and biofilm formation, not by regulating type IV pili-associated genes expression, but by regulating the chaperone/usher pili-associated csuA/ABCDE operon and the AbaI-dependent quorum-sensing pathway-associated A1S_0112-0119 operon instead.

Keywords: Acinetobacter baumannii; biofilm formation; motility; pili; quorum sensing; two-component systems.

MeSH terms

  • Acinetobacter baumannii / physiology*
  • Acinetobacter baumannii / ultrastructure
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Biofilms*
  • Gene Deletion
  • Gene Expression Profiling
  • Gene Expression Regulation, Bacterial
  • Gene Knockout Techniques
  • Gene Order
  • Histidine Kinase / chemistry
  • Histidine Kinase / genetics*
  • Histidine Kinase / metabolism*
  • Lactones / metabolism
  • Operon
  • Phenotype
  • Quorum Sensing*

Substances

  • Bacterial Proteins
  • Lactones
  • Histidine Kinase