The Flagellar Gene Regulates Biofilm Formation and Mussel Larval Settlement and Metamorphosis

Int J Mol Sci. 2020 Jan 21;21(3):710. doi: 10.3390/ijms21030710.

Abstract

Biofilms are critical components of most marine systems and provide biochemical cues that can significantly impact overall community composition. Although progress has been made in the bacteria-animal interaction, the molecular basis of modulation of settlement and metamorphosis in most marine animals by bacteria is poorly understood. Here, Pseudoalteromonas marina showing inducing activity on mussel settlement and metamorphosis was chosen as a model to clarify the mechanism that regulates the bacteria-mussel interaction. We constructed a flagellin synthetic protein gene fliP deletion mutant of P. marina and checked whether deficiency of fliP gene will impact inducing activity, motility, and extracellular polymeric substances of biofilms. Furthermore, we examined the effect of flagellar proteins extracted from bacteria on larval settlement and metamorphosis. The deletion of the fliP gene caused the loss of the flagella structure and motility of the ∆fliP strain. Deficiency of the fliP gene promoted the biofilm formation and changed biofilm matrix by reducing β-polysaccharides and increasing extracellular proteins and finally reduced biofilm-inducing activities. Flagellar protein extract promoted mussel metamorphosis, and ∆fliP biofilms combined with additional flagellar proteins induced similar settlement and metamorphosis rate compared to that of the wild-type strain. These findings provide novel insight on the molecular interactions between bacteria and mussels.

Keywords: Mytilus coruscus; biofilm; flagellar gene; larval settlement and metamorphosis; mussel.

MeSH terms

  • Animals
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Biofilms / growth & development*
  • Bivalvia / microbiology
  • Bivalvia / physiology*
  • China
  • Flagellin / genetics*
  • Flagellin / metabolism
  • Host Microbial Interactions / genetics
  • Host Microbial Interactions / physiology*
  • Larva / microbiology
  • Larva / physiology*
  • Marine Biology
  • Metamorphosis, Biological / physiology*
  • Mutation
  • Mytilus / microbiology
  • Mytilus / physiology
  • Pseudoalteromonas / cytology
  • Pseudoalteromonas / genetics*
  • Pseudoalteromonas / physiology
  • Transcriptome

Substances

  • Bacterial Proteins
  • Flagellin
  • FliP protein, Bacillus